Gastric Residual VolumeNCT05888090
The Effect of Position Given to Preterms After Feeding on Gastric Residual Volume, Abdominal Oxygenation and Fractional Oxygen Extraction
A study testing Prone, right lateral, and semi-elevated supine positions, Semi-elevated supine, prone, and right lateral positions and Right lateral, semi-elevated supine, and prone positions in people with Gastric Residual Volume and Abdominal Oxygenation, run by Istanbul University - Cerrahpasa at 1 site in Turkey (Türkiye).
Trial summary
This study is a PhD dissertation. In this study, the investigators aim to investigate the effects of three different positions after feeding on gastric residual volume, abdominal oxygenation using near infrared spectroscopy (NIRS), and fractional oxygen extraction values in preterm newborns. Read more about this study
- Who is it for?
- Ages 28 to 33 weeks
- Conditions the study is for
- Gastric Residual Volume, Abdominal Oxygenation, Fractional Oxygen Extraction
- What is being tested?
- Prone, right lateral, and semi-elevated supine positions, Semi-elevated supine, prone, and right lateral positions and Right lateral, semi-elevated supine, and prone positions
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 48 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 1 Sep 2023to 4 Jun 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 28 to 33 weeks
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- Preterm newborns who are at 28-33 weeks of gestation according to the last menstrual period of the mother,
- Preterm newborns who are breastfed,
- Preterm newborns who are clinically stable and enteral feeding started,
- Preterm newborns who are first enteral nutrition 24 hours after mechanical ventilation,
- Preterm newborns who are at least 50% of their nutrition provided with enteral nutrition,
- Free Newborns fed by flow and orogastric tube and with informed consent of the parents will be included in the study.
Who cannot join
- Preterm newborns requiring mechanical ventilation,
- Preterm newborns diagnosed with NEC,
- Preterm newborns vomiting,
- Preterm newborns who have abdominal distension,
- Preterm newborns who have nasal mechanical obstruction,
- Preterm newborns who have congenital anomalies,
Show all 9Show fewer
- Preterm newborns who have gastrointestinal problems such as gastroschisis or congenital diaphragmatic hernia,
- Preterm newborn who have cerebrovascular disease, apnea episodes, severe neurological disease, were included in the study. will not be included,
- Preterm newborns who worsen clinically after inclusion in the sample group will be excluded from the study.
Trial locations and contacts
1 site in 1 country.
About this study
This study is a PhD dissertation. In this study, the investigators aim to investigate the effects of three different positions after feeding on gastric residual volume, abdominal oxygenation using near infrared spectroscopy (NIRS), and fractional oxygen extraction values in preterm newborns.
Read the detailed description
The Design of Research
This study was planned in a randomized crossover study design to evaluate the effects of three different positions on gastric residual volume, fractional oxygen extraction and abdominal oxygenation in clinically stable breastfed preterm newborns. The order of the 3 positions that will be given to the participants the research group will be determined by drawing lots and 3 intervention groups will be formed. The participants in each intervention group will be followed for two hours after feeding in all three positions: semi-elevated supine position, prone position, and right lateral position. Positions will be given to the participants, taking into account the order of positions in each group. All positions will be applied once to each participant. Groups and position rankings according to the result of the draw:
- st group: Prone, right lateral, and semi-elevated supine position;
- nd group: Semi-elevated supine, prone, and right lateral position;
- rd group: Right lateral, semi-elevated supine, and prone position;
48 participants in the study group will be randomly assigned to these 3 intervention groups. In order to determine which participant will be in which group, the numbers from 1 to 48 were distributed to 3 groups through a program in the computer environment without repeating the number (https://www.randomizer.org/). Randomization is provided as follows.
Intervention group 1: 2.8,12,17,18,22,24,25,26,31,33,36,37,40,42,45; Intervention group 2: 1,3,5,10,14,16,19,20,27,28,29,30,32,34,43,44; Intervention group 3: 4,6,7,9,11,13,15,21,23,35,38,39,41,46,47,48;
Location and Time of Research Data of the research Istanbul Kartal Dr. Lütfi Kırdar City Hospital will meet at the Newborn Intensive Care Unit between July 2023 and July 2024. 2., 3., and the university hospital, which provides 4A level intensive care, consists of a total of 41 beds. It consists of 14 level beds, 3rd level 14 beds and 13 beds with 4A level.
Survey's Universe and Sampling After the necessary legal permits have been obtained in the universe of the research, (Ethical Board approval and institution permit ), Kartal Dr. at the time of the investigation. The preterm followed by the Lütfi Kırdar City Hospital Newborn Intensive Care Unit will create newborns.
The sample of the research is Eagle Dr. Lütfi Kırdar City Hospital will create 48 preterm newborns with 28-33 gestation weeks, which are hospitalized between March 2023 and March 2024, which meet the inclusion criteria and received written consent from their parents. Intake swallowing coordination but 32-34. Since it develops after the gestation week, (Törüner ve Büyükgönenç, 2012) sampling will be included in preterm newborns smaller than the 34th gestation week.
Power analysis was performed using the G*Power (v3.1.9.2) program to determine the number of samples. The strength of the study is 1-β (β = II. The probability of type error is expressed as ) and in general research should have 80% power. S. S. Based on the study of Ceylan et al, the effect size of the calculation result made based on the difference of Gastric residuals (ml) measurements according to the supine and right lateral position was calculated as d=0.420 and at the level of α=0.05 %It has been calculated that there must be at least 47 preterm newborns in total to get 80 powers. Considering the loss of case, the number of samples was determined as 48.
Inclusion criteria; The participants who are in the 28-33 gestation week according to the mother's last men's history, are the 1st enteral feeding after mechanical ventilation, fed with breast milk, clinically stable and enteral nutrition, Newborns provided with at least 50% ' of enteral nutrition, fed with free flow and orogastric probe, and received informed consent from parents will be included in the study.
Exclusion criteria; With cerebrovascular disease, with a need for mechanical ventilation, diagnosed with NEC, vomiting, abdominal distension, nasal mechanical obstruction, congenital anomaly, gastrochysis or congenital diaphragm hernia, Newborns with apnea episodes, severe neurological disease will not be included in the study. The participants that worsen clinically after being included in the sample group will be removed from the study.
Independent variables: Positioning (Prone, right lateral and semi-elevated supine position) Dependent variables: Preterm newborn abdominal NIRS value, fractional oxygen extraction value, gastric residual volume.
Research Hypotheses H0: There is no difference between the effects of the three positions on gastric residual volume, abdominal oxygenation, and fractional oxygen extraction.
H1: Abdominal oxygenation and oxygen level (SPO2) are higher in the prone position than in the semi-elevated supine position and the right lateral position.
H2: Abdominal oxygenation and oxygen level (SPO2) are higher in the right lateral position than in the semi-elevated supine position.
H3: The amount of gastric residual volume in the prone position is lower than in the semi-elevated supine position and the right lateral position.
H4: The amount of gastric residual volume in the right lateral position is lower than in the semi-elevated supine position.
H5: Fractional oxygen extraction in the prone position is lower than in the right lateral and semi-elevated supine position.
Data Collection Method The data were collected from Kartal Dr. It will be collected in the neonatal intensive care unit of Lütfi Kırdar City Hospital. Study data will be collected by two investigators. The investigators responsible for the study, the subjects, and the statistician who will analyze the study will be blinded to the data. In the study, the blinding technique was planned as three blinds.
I ntroductory Information and Data Collection Form The intervention group of each participant included in the sample, week of gestation (according to last menstrual period), date, type of delivery, postnatal age, birth weight, postnatal body weight, gender, receiving intravenous fluid support, mean NIRS value, heart rate, and saturation value, amount and color of gastric residual volume before feeding, presence of a disease requiring medical treatment will be recorded.
To assess abdominal oxygenation (ArSO2), the NIRS sensor probe will be placed over the lower abdomen (under the umbilicus) and monitored. The participants who meet the inclusion criteria will be monitored through the NIRS for three feedings. Average NIRS values will be calculated for periods immediately before, during and after feeding. NIRS values will be recorded by the monitor, after the monitoring, the picture of the records will be taken from the monitor. During the follow-up, the location of the probe and the NIRS value will be followed by the investigators who collect data. The probe position will be changed to be in the lower abdomen before each feeding during the follow-up period. While NIRS values are recorded, pulse oximetry values will also be recorded.
Materials to be Used
- Gastric residual volume Gastric residual volume will be checked manually using a 5 ml syringe prior to feeding. Gastric residue will be excreted or given back in consultation with the doctor according to its amount and color.
- Breast Milk: Name and date control of the milk stored in milk storage bags in the refrigerator will be made. The breast milk drawn into the injector in accordance with the hygiene rules will be given to the participants after it reaches the appropriate temperature (must be at body temperature) in hot water. Heating breast milk above 40°C is not recommended as it will destroy immunologically active factors.
- Positioning: Participants will be placed in the supine position during feeding. Feeding will be done every 2-3 hours. Participants will be positioned in one position for 2 hours after feeding.
- Semi-elevated supine position
- prone position
- Right lateral position
Data Collection Feeding time will take 10-20 minutes. The participants will be included in the sampling from their 1st feeding after weaning off the mechanical ventilator. The procedure will begin when participants in all groups are calm. The entire application process will be carried out in the neonatal intensive care unit and all materials will be prepared before the procedure. In all three intervention groups, gastric residue will be checked with a 5 ml injector just before feeding, and the residual content will be discarded or returned with the decision of the doctor. The NIRS sensor probe will be attached to the lower abdomen. Since the cost of the probes is high, reversebl probes will be used and their cleaning will be provided with high-level disinfectant (Ecolab wipes). One NIRS probe will be used for two participants. The same enteral feeding protocol will be applied to all participants. In the institution where the study will be conducted, minimal enteral nutrition is started in participants, with breast milk being the first choice after 24 hours postnatally. Then, if the participant can tolerate enteral feeding, the amount is gradually increased each day. Decisions to increase feeding volume, stop feeding and use breast milk fortifier are made by the clinical team based on local protocols. The amount and frequency of feeding will be decided according to the gestational week, body weight and clinical condition of the participant.
Data Analysis NCSS (Number Cruncher Statistical System) 2020 Statistical Software (NCSS LLC, Kaysville, Utah, USA) program will be used for statistical analysis. While evaluating the study data, Shapiro Wilks test and Box Plot charts will be used to evaluate the conformity of the data to the normal distribution, as well as descriptive statistical methods (mean, standard deviation, median, frequency and ratio). Student's t test in the evaluation of two groups of normally distributed variables; Oneway Anova test will be used in the comparison of three groups and above, and the Bonferroni test will be used to determine the group that causes the difference. Repeated Measures test for evaluations according to three positions within the group; Bonferroni test will be used in post hoc evaluations and Paired Sample t test will be used in peer-to-peer evaluations. Mann Whitney U test in the evaluation of non-normally distributed variables according to two groups; Kruskal Wallis test will be used in the comparison of three groups and above, and Dunn test will be used to determine the group causing the difference. Friedman test post hoc Dunn test in the evaluations according to three positions within the group; Wilcoxon Signed Rank test will be used for peer-to-peer evaluations. Pearson or Spearman's correlation analysis will be used according to the distribution in the evaluation of the relations between the variables; Linear regression models will be made in further evaluations. Chi-square test and Fisher's Exact test will be used in the comparison of qualitative data. The results will be evaluated at the 95% confidence interval, at the p<0.05 level of significance.
- Conditions
- Gastric Residual Volume, Abdominal Oxygenation, Fractional Oxygen Extraction, Positioning (Prone, Right Lateral and Semi-Elevated Supine Position)
- Being tested
- Prone, right lateral, and semi-elevated supine positions, Semi-elevated supine, prone, and right lateral positions, Right lateral, semi-elevated supine, and prone positions
- Keywords
- Preterm Infants, Positioning, Gastric Residual Volume, Abdominal Oxygenation, Fractional Oxygen Extraction
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Prone, right lateral, and semi-elevated supine positionsOther
Each participant will be followed during three feedings and the prone, right lateral, and semi-elevated supine positions will be applied once.
Semi-elevated supine, prone, and right lateral positionsOther
Each participant will be followed during three feedings and the semi-elevated supine, prone, and right lateral positions will be applied once.
Right lateral, semi-elevated supine, and prone positionsOther
Each participant will be followed during three feedings and the right lateral, semi-elevated supine, and prone positions will be applied once.
| Study group | Role | What they receive |
|---|---|---|
| Intervention Group 1 | Experimental | Not described Receives: Other: Prone, right lateral, and semi-elevated supine positions |
| Intervention Group 2 | Experimental | Not described Receives: Other: Semi-elevated supine, prone, and right lateral positions |
| Intervention Group 3 | Experimental | Not described Receives: Other: Right lateral, semi-elevated supine, and prone positions |
What is being measured
The primary outcome is the main question the study is designed to answer.
Preterm newborn abdominal NIRS value
Average NIRS values will be calculated for periods immediately before, during and after feeding. NIRS values will be recorded by the device, after the monitoring, the picture of the records will be taken from the device.
Measured: Preterm newborns whose feedings are every two hours will be monitored for 6 hours and those whose feedings are every three hours will be monitored for 9 hours. Preterm newborns will be monitored for a total of three feedings
Fractional oxygen extraction value
Pulse oximeter and NIRS monitor will be used together to determine fractional oxygen extraction.
Measured: Preterm newborns whose feedings are every two hours will be monitored for 6 hours and those whose feedings are every three hours will be monitored for 9 hours. Preterm newborns will be monitored for a total of three feedings
Gastric residual volume
Gastric residual volume will be checked manually using a 5 ml syringe prior to feeding. Gastric residue will be excreted or given back in consultation with the doctor according to its amount and color.
Measured: Preterm newborns whose feedings are every two hours will be monitored for 6 hours and those whose feedings are every three hours will be monitored for 9 hours. Preterm newborns will be monitored for a total of three feedings
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Jun 2023
- Study start1 Sep 2023
- Primary completion1 Aug 2024
- Study completion4 Jun 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (23)Papers the sponsor has linked to this study.
- Other trials for Gastric Residual VolumeStudies of the same condition, open and under way.
- More trials run by Istanbul University - CerrahpasaThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Crossover
- Model description
- Breastfed preterm neonates to be included in the study will be placed in 3 positions in a randomized crossover design. The order of the 3 positions that will be given to the babies in the research group will be determined by drawing lots and 3 intervention groups will be formed. Preterm newborns in each intervention group will be followed for two hours after feeding in all three positions: semi-elevated supine position, prone position, and right lateral position. Positions will be given to babies, taking into account the order of positions in each group. All positions will be applied once to each baby. Groups and position rankings according to the result of the draw: 1. st group: Prone, right lateral and semi-raised supine position 2. nd group: Semi-raised supine, prone and right lateral position 3. rd group: Right lateral, semi-raised supine and prone position 48 preterm newborns in the study group will be randomly assigned to these 3 intervention groups.
- Masking
- None (open label)
- Enrolment
- 48 participants (actual)
Sponsor and investigators
- Lead sponsor
- Istanbul University - Cerrahpasa
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, HANDE OZGORU, Istanbul University - Cerrahpasa
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05888090
- Sponsor's protocol ID
- 14311537094
- Status last verified
- Jul 2025
- First submitted
- 24 May 2023
- Last updated
- 24 Jul 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Boquien CY. Human Milk: An Ideal Food for Nutrition of Preterm Newborn. Front Pediatr. 2018 Oct 16;6:295. doi: 10.3389/fped.2018.00295. eCollection 2018.
PubMed 30386758Braski K, Weaver-Lewis K, Loertscher M, Ding Q, Sheng X, Baserga M. Splanchnic-Cerebral Oxygenation Ratio Decreases during Enteral Feedings in Anemic Preterm Infants: Observations under Near-Infrared Spectroscopy. Neonatology. 2018;113(1):75-80. doi: 10.1159/000481396. Epub 2017 Nov 8.
PubMed 29131125Barsan Kaya T, Aydemir O, Tekin AN. Prone versus supine position for regional cerebral tissue oxygenation in preterm neonates receiving noninvasive ventilation. J Matern Fetal Neonatal Med. 2021 Oct;34(19):3127-3132. doi: 10.1080/14767058.2019.1678133. Epub 2019 Oct 15.
PubMed 31615310Chen SS, Tzeng YL, Gau BS, Kuo PC, Chen JY. Effects of prone and supine positioning on gastric residuals in preterm infants: a time series with cross-over study. Int J Nurs Stud. 2013 Nov;50(11):1459-67. doi: 10.1016/j.ijnurstu.2013.02.009. Epub 2013 Mar 26.
PubMed 23537895Corvaglia L, Martini S, Battistini B, Rucci P, Aceti A, Faldella G. Bolus vs. continuous feeding: effects on splanchnic and cerebral tissue oxygenation in healthy preterm infants. Pediatr Res. 2014 Jul;76(1):81-5. doi: 10.1038/pr.2014.52. Epub 2014 Apr 8.
PubMed 24713819Corvaglia L, Martini S, Battistini B, Rucci P, Faldella G, Aceti A. Splanchnic Oxygenation at First Enteral Feeding in Preterm Infants: Correlation With Feeding Intolerance. J Pediatr Gastroenterol Nutr. 2017 Apr;64(4):550-554. doi: 10.1097/MPG.0000000000001308.
PubMed 27467111Cortez J, Makker K, Kraemer DF, Neu J, Sharma R, Hudak ML. Maternal milk feedings reduce sepsis, necrotizing enterocolitis and improve outcomes of premature infants. J Perinatol. 2018 Jan;38(1):71-74. doi: 10.1038/jp.2017.149. Epub 2017 Sep 28.
PubMed 29048409Ceylan SS, Keskin Z. Effects of two different positions on stress, pain and feeding tolerance of preterm infants during tube feeding. Int J Nurs Pract. 2021 Oct;27(5):e12911. doi: 10.1111/ijn.12911. Epub 2020 Dec 9.
PubMed 33300212da Costa CS, Greisen G, Austin T. Is near-infrared spectroscopy clinically useful in the preterm infant? Arch Dis Child Fetal Neonatal Ed. 2015 Nov;100(6):F558-61. doi: 10.1136/archdischild-2014-307919. Epub 2015 Jul 27.
PubMed 26215405Demirel G, Oguz SS, Celik IH, Erdeve O, Dilmen U. Cerebral and mesenteric tissue oxygenation by positional changes in very low birth weight premature infants. Early Hum Dev. 2012 Jun;88(6):409-11. doi: 10.1016/j.earlhumdev.2011.10.005. Epub 2011 Nov 15.
PubMed 22088784Dani C, Coviello C, Montano S, Remaschi G, Petrolini C, Strozzi MC, Maggiora E, Sabatini M, Gazzolo D. Effect on splanchnic oxygenation of breast milk, fortified breast milk, and formula milk in preterm infants. Pediatr Res. 2021 Jan;89(1):171-174. doi: 10.1038/s41390-020-0935-1. Epub 2020 May 7.
PubMed 32380507Garvey AA, Dempsey EM. Applications of near infrared spectroscopy in the neonate. Curr Opin Pediatr. 2018 Apr;30(2):209-215. doi: 10.1097/MOP.0000000000000599.
PubMed 29369068Goldshtrom N, Isler JR, Sahni R. Comparing liver and lower abdomen near-infrared spectroscopy in preterm infants. Early Hum Dev. 2020 Dec;151:105194. doi: 10.1016/j.earlhumdev.2020.105194. Epub 2020 Sep 17.
PubMed 33017708Hay WW Jr, Hendrickson KC. Preterm formula use in the preterm very low birth weight infant. Semin Fetal Neonatal Med. 2017 Feb;22(1):15-22. doi: 10.1016/j.siny.2016.08.005. Epub 2016 Aug 30.
PubMed 27595621Liao SM, Rao R, Mathur AM. Head Position Change Is Not Associated with Acute Changes in Bilateral Cerebral Oxygenation in Stable Preterm Infants during the First 3 Days of Life. Am J Perinatol. 2015 Jun;32(7):645-52. doi: 10.1055/s-0034-1390348. Epub 2014 Oct 5.
PubMed 25282608
Study at a glance
From the registry record, last updated by the sponsor on 24 Jul 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Position Given to Preterms After Feeding on Gastric Residual Volume, Abdominal Oxygenation and Fractional Oxygen Extraction
- ClinicalTrials.gov ID
- NCT05888090
- Acronym / sponsor ID
- 14311537094
- Conditions
- Gastric Residual Volume, Abdominal Oxygenation, Fractional Oxygen Extraction, Positioning (Prone, Right Lateral and Semi-Elevated Supine Position)
- Keywords
- Preterm Infants, Positioning, Gastric Residual Volume, Abdominal Oxygenation, Fractional Oxygen Extraction
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 48 participants (actual)
- Lead sponsor
- Istanbul University - CerrahpasaUniversity, hospital or other
- Study start
- 1 Sep 2023 (actual)
- Primary completion
- 1 Aug 2024 (actual)
- Study completion
- 4 Jun 2025 (actual)
- First posted
- 5 Jun 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study is a PhD dissertation. In this study, the investigators aim to investigate the effects of three different positions after feeding on gastric residual volume, abdominal oxygenation using near infrared spectroscopy (NIRS), and fractional oxygen extraction values in preterm newborns.
Detailed description
The Design of Research
This study was planned in a randomized crossover study design to evaluate the effects of three different positions on gastric residual volume, fractional oxygen extraction and abdominal oxygenation in clinically stable breastfed preterm newborns. The order of the 3 positions that will be given to the participants the research group will be determined by drawing lots and 3 intervention groups will be formed. The participants in each intervention group will be followed for two hours after feeding in all three positions: semi-elevated supine position, prone position, and right lateral position. Positions will be given to the participants, taking into account the order of positions in each group. All positions will be applied once to each participant. Groups and position rankings according to the result of the draw:
- st group: Prone, right lateral, and semi-elevated supine position;
- nd group: Semi-elevated supine, prone, and right lateral position;
- rd group: Right lateral, semi-elevated supine, and prone position;
48 participants in the study group will be randomly assigned to these 3 intervention groups. In order to determine which participant will be in which group, the numbers from 1 to 48 were distributed to 3 groups through a program in the computer environment without repeating the number (https://www.randomizer.org/). Randomization is provided as follows.
Intervention group 1: 2.8,12,17,18,22,24,25,26,31,33,36,37,40,42,45; Intervention group 2: 1,3,5,10,14,16,19,20,27,28,29,30,32,34,43,44; Intervention group 3: 4,6,7,9,11,13,15,21,23,35,38,39,41,46,47,48;
Location and Time of Research Data of the research Istanbul Kartal Dr. Lütfi Kırdar City Hospital will meet at the Newborn Intensive Care Unit between July 2023 and July 2024. 2., 3., and the university hospital, which provides 4A level intensive care, consists of a total of 41 beds. It consists of 14 level beds, 3rd level 14 beds and 13 beds with 4A level.
Survey's Universe and Sampling After the necessary legal permits have been obtained in the universe of the research, (Ethical Board approval and institution permit ), Kartal Dr. at the time of the investigation. The preterm followed by the Lütfi Kırdar City Hospital Newborn Intensive Care Unit will create newborns.
The sample of the research is Eagle Dr. Lütfi Kırdar City Hospital will create 48 preterm newborns with 28-33 gestation weeks, which are hospitalized between March 2023 and March 2024, which meet the inclusion criteria and received written consent from their parents. Intake swallowing coordination but 32-34. Since it develops after the gestation week, (Törüner ve Büyükgönenç, 2012) sampling will be included in preterm newborns smaller than the 34th gestation week.
Power analysis was performed using the G*Power (v3.1.9.2) program to determine the number of samples. The strength of the study is 1-β (β = II. The probability of type error is expressed as ) and in general research should have 80% power. S. S. Based on the study of Ceylan et al, the effect size of the calculation result made based on the difference of Gastric residuals (ml) measurements according to the supine and right lateral position was calculated as d=0.420 and at the level of α=0.05 %It has been calculated that there must be at least 47 preterm newborns in total to get 80 powers. Considering the loss of case, the number of samples was determined as 48.
Inclusion criteria; The participants who are in the 28-33 gestation week according to the mother's last men's history, are the 1st enteral feeding after mechanical ventilation, fed with breast milk, clinically stable and enteral nutrition, Newborns provided with at least 50% ' of enteral nutrition, fed with free flow and orogastric probe, and received informed consent from parents will be included in the study.
Exclusion criteria; With cerebrovascular disease, with a need for mechanical ventilation, diagnosed with NEC, vomiting, abdominal distension, nasal mechanical obstruction, congenital anomaly, gastrochysis or congenital diaphragm hernia, Newborns with apnea episodes, severe neurological disease will not be included in the study. The participants that worsen clinically after being included in the sample group will be removed from the study.
Independent variables: Positioning (Prone, right lateral and semi-elevated supine position) Dependent variables: Preterm newborn abdominal NIRS value, fractional oxygen extraction value, gastric residual volume.
Research Hypotheses H0: There is no difference between the effects of the three positions on gastric residual volume, abdominal oxygenation, and fractional oxygen extraction.
H1: Abdominal oxygenation and oxygen level (SPO2) are higher in the prone position than in the semi-elevated supine position and the right lateral position.
H2: Abdominal oxygenation and oxygen level (SPO2) are higher in the right lateral position than in the semi-elevated supine position.
H3: The amount of gastric residual volume in the prone position is lower than in the semi-elevated supine position and the right lateral position.
H4: The amount of gastric residual volume in the right lateral position is lower than in the semi-elevated supine position.
H5: Fractional oxygen extraction in the prone position is lower than in the right lateral and semi-elevated supine position.
Data Collection Method The data were collected from Kartal Dr. It will be collected in the neonatal intensive care unit of Lütfi Kırdar City Hospital. Study data will be collected by two investigators. The investigators responsible for the study, the subjects, and the statistician who will analyze the study will be blinded to the data. In the study, the blinding technique was planned as three blinds.
I ntroductory Information and Data Collection Form The intervention group of each participant included in the sample, week of gestation (according to last menstrual period), date, type of delivery, postnatal age, birth weight, postnatal body weight, gender, receiving intravenous fluid support, mean NIRS value, heart rate, and saturation value, amount and color of gastric residual volume before feeding, presence of a disease requiring medical treatment will be recorded.
To assess abdominal oxygenation (ArSO2), the NIRS sensor probe will be placed over the lower abdomen (under the umbilicus) and monitored. The participants who meet the inclusion criteria will be monitored through the NIRS for three feedings. Average NIRS values will be calculated for periods immediately before, during and after feeding. NIRS values will be recorded by the monitor, after the monitoring, the picture of the records will be taken from the monitor. During the follow-up, the location of the probe and the NIRS value will be followed by the investigators who collect data. The probe position will be changed to be in the lower abdomen before each feeding during the follow-up period. While NIRS values are recorded, pulse oximetry values will also be recorded.
Materials to be Used
- Gastric residual volume Gastric residual volume will be checked manually using a 5 ml syringe prior to feeding. Gastric residue will be excreted or given back in consultation with the doctor according to its amount and color.
- Breast Milk: Name and date control of the milk stored in milk storage bags in the refrigerator will be made. The breast milk drawn into the injector in accordance with the hygiene rules will be given to the participants after it reaches the appropriate temperature (must be at body temperature) in hot water. Heating breast milk above 40°C is not recommended as it will destroy immunologically active factors.
- Positioning: Participants will be placed in the supine position during feeding. Feeding will be done every 2-3 hours. Participants will be positioned in one position for 2 hours after feeding.
- Semi-elevated supine position
- prone position
- Right lateral position
Data Collection Feeding time will take 10-20 minutes. The participants will be included in the sampling from their 1st feeding after weaning off the mechanical ventilator. The procedure will begin when participants in all groups are calm. The entire application process will be carried out in the neonatal intensive care unit and all materials will be prepared before the procedure. In all three intervention groups, gastric residue will be checked with a 5 ml injector just before feeding, and the residual content will be discarded or returned with the decision of the doctor. The NIRS sensor probe will be attached to the lower abdomen. Since the cost of the probes is high, reversebl probes will be used and their cleaning will be provided with high-level disinfectant (Ecolab wipes). One NIRS probe will be used for two participants. The same enteral feeding protocol will be applied to all participants. In the institution where the study will be conducted, minimal enteral nutrition is started in participants, with breast milk being the first choice after 24 hours postnatally. Then, if the participant can tolerate enteral feeding, the amount is gradually increased each day. Decisions to increase feeding volume, stop feeding and use breast milk fortifier are made by the clinical team based on local protocols. The amount and frequency of feeding will be decided according to the gestational week, body weight and clinical condition of the participant.
Data Analysis NCSS (Number Cruncher Statistical System) 2020 Statistical Software (NCSS LLC, Kaysville, Utah, USA) program will be used for statistical analysis. While evaluating the study data, Shapiro Wilks test and Box Plot charts will be used to evaluate the conformity of the data to the normal distribution, as well as descriptive statistical methods (mean, standard deviation, median, frequency and ratio). Student's t test in the evaluation of two groups of normally distributed variables; Oneway Anova test will be used in the comparison of three groups and above, and the Bonferroni test will be used to determine the group that causes the difference. Repeated Measures test for evaluations according to three positions within the group; Bonferroni test will be used in post hoc evaluations and Paired Sample t test will be used in peer-to-peer evaluations. Mann Whitney U test in the evaluation of non-normally distributed variables according to two groups; Kruskal Wallis test will be used in the comparison of three groups and above, and Dunn test will be used to determine the group causing the difference. Friedman test post hoc Dunn test in the evaluations according to three positions within the group; Wilcoxon Signed Rank test will be used for peer-to-peer evaluations. Pearson or Spearman's correlation analysis will be used according to the distribution in the evaluation of the relations between the variables; Linear regression models will be made in further evaluations. Chi-square test and Fisher's Exact test will be used in the comparison of qualitative data. The results will be evaluated at the 95% confidence interval, at the p<0.05 level of significance.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Number of arms
- 3
- Model description
- Breastfed preterm neonates to be included in the study will be placed in 3 positions in a randomized crossover design. The order of the 3 positions that will be given to the babies in the research group will be determined by drawing lots and 3 intervention groups will be formed. Preterm newborns in each intervention group will be followed for two hours after feeding in all three positions: semi-elevated supine position, prone position, and right lateral position. Positions will be given to babies, taking into account the order of positions in each group. All positions will be applied once to each baby. Groups and position rankings according to the result of the draw: 1. st group: Prone, right lateral and semi-raised supine position 2. nd group: Semi-raised supine, prone and right lateral position 3. rd group: Right lateral, semi-raised supine and prone position 48 preterm newborns in the study group will be randomly assigned to these 3 intervention groups.
| Arm | Type | Receives |
|---|---|---|
| Intervention Group 1 | Experimental | Other: Prone, right lateral, and semi-elevated supine positions |
| Intervention Group 2 | Experimental | Other: Semi-elevated supine, prone, and right lateral positions |
| Intervention Group 3 | Experimental | Other: Right lateral, semi-elevated supine, and prone positions |
Who may qualify
- Ages
- 28 to 33 weeks
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (6 listed)
- Preterm newborns who are at 28-33 weeks of gestation according to the last menstrual period of the mother,
- Preterm newborns who are breastfed,
- Preterm newborns who are clinically stable and enteral feeding started,
- Preterm newborns who are first enteral nutrition 24 hours after mechanical ventilation,
- Preterm newborns who are at least 50% of their nutrition provided with enteral nutrition,
Key exclusion criteria (9 listed)
- Preterm newborns requiring mechanical ventilation,
- Preterm newborns diagnosed with NEC,
- Preterm newborns vomiting,
- Preterm newborns who have abdominal distension,
- Preterm newborns who have nasal mechanical obstruction,
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Prone, right lateral, and semi-elevated supine positionsEach participant will be followed during three feedings and the prone, right lateral, and semi-elevated supine positions will be applied once. | Other | Intervention Group 1 |
| Semi-elevated supine, prone, and right lateral positionsEach participant will be followed during three feedings and the semi-elevated supine, prone, and right lateral positions will be applied once. | Other | Intervention Group 2 |
| Right lateral, semi-elevated supine, and prone positionsEach participant will be followed during three feedings and the right lateral, semi-elevated supine, and prone positions will be applied once. | Other | Intervention Group 3 |
Primary outcome
Preterm newborn abdominal NIRS value
Time frame: Preterm newborns whose feedings are every two hours will be monitored for 6 hours and those whose feedings are every three hours will be monitored for 9 hours. Preterm newborns will be monitored for a total of three feedings
Average NIRS values will be calculated for periods immediately before, during and after feeding. NIRS values will be recorded by the device, after the monitoring, the picture of the records will be taken from the device.
Fractional oxygen extraction value
Time frame: Preterm newborns whose feedings are every two hours will be monitored for 6 hours and those whose feedings are every three hours will be monitored for 9 hours. Preterm newborns will be monitored for a total of three feedings
Pulse oximeter and NIRS monitor will be used together to determine fractional oxygen extraction.
Gastric residual volume
Time frame: Preterm newborns whose feedings are every two hours will be monitored for 6 hours and those whose feedings are every three hours will be monitored for 9 hours. Preterm newborns will be monitored for a total of three feedings
Gastric residual volume will be checked manually using a 5 ml syringe prior to feeding. Gastric residue will be excreted or given back in consultation with the doctor according to its amount and color.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Jul 2025.
- Background: PubMed 30386758Boquien CY. Human Milk: An Ideal Food for Nutrition of Preterm Newborn. Front Pediatr. 2018 Oct 16;6:295. doi: 10.3389/fped.2018.00295. eCollection 2018.
- Background: PubMed 29131125Braski K, Weaver-Lewis K, Loertscher M, Ding Q, Sheng X, Baserga M. Splanchnic-Cerebral Oxygenation Ratio Decreases during Enteral Feedings in Anemic Preterm Infants: Observations under Near-Infrared Spectroscopy. Neonatology. 2018;113(1):75-80. doi: 10.1159/000481396. Epub 2017 Nov 8.
- Background: PubMed 31615310Barsan Kaya T, Aydemir O, Tekin AN. Prone versus supine position for regional cerebral tissue oxygenation in preterm neonates receiving noninvasive ventilation. J Matern Fetal Neonatal Med. 2021 Oct;34(19):3127-3132. doi: 10.1080/14767058.2019.1678133. Epub 2019 Oct 15.
- Background: PubMed 23537895Chen SS, Tzeng YL, Gau BS, Kuo PC, Chen JY. Effects of prone and supine positioning on gastric residuals in preterm infants: a time series with cross-over study. Int J Nurs Stud. 2013 Nov;50(11):1459-67. doi: 10.1016/j.ijnurstu.2013.02.009. Epub 2013 Mar 26.
- Background: PubMed 24713819Corvaglia L, Martini S, Battistini B, Rucci P, Aceti A, Faldella G. Bolus vs. continuous feeding: effects on splanchnic and cerebral tissue oxygenation in healthy preterm infants. Pediatr Res. 2014 Jul;76(1):81-5. doi: 10.1038/pr.2014.52. Epub 2014 Apr 8.
- Background: PubMed 27467111Corvaglia L, Martini S, Battistini B, Rucci P, Faldella G, Aceti A. Splanchnic Oxygenation at First Enteral Feeding in Preterm Infants: Correlation With Feeding Intolerance. J Pediatr Gastroenterol Nutr. 2017 Apr;64(4):550-554. doi: 10.1097/MPG.0000000000001308.
- Background: PubMed 29048409Cortez J, Makker K, Kraemer DF, Neu J, Sharma R, Hudak ML. Maternal milk feedings reduce sepsis, necrotizing enterocolitis and improve outcomes of premature infants. J Perinatol. 2018 Jan;38(1):71-74. doi: 10.1038/jp.2017.149. Epub 2017 Sep 28.
- Background: PubMed 33300212Ceylan SS, Keskin Z. Effects of two different positions on stress, pain and feeding tolerance of preterm infants during tube feeding. Int J Nurs Pract. 2021 Oct;27(5):e12911. doi: 10.1111/ijn.12911. Epub 2020 Dec 9.
- Background: PubMed 26215405da Costa CS, Greisen G, Austin T. Is near-infrared spectroscopy clinically useful in the preterm infant? Arch Dis Child Fetal Neonatal Ed. 2015 Nov;100(6):F558-61. doi: 10.1136/archdischild-2014-307919. Epub 2015 Jul 27.
- Background: PubMed 22088784Demirel G, Oguz SS, Celik IH, Erdeve O, Dilmen U. Cerebral and mesenteric tissue oxygenation by positional changes in very low birth weight premature infants. Early Hum Dev. 2012 Jun;88(6):409-11. doi: 10.1016/j.earlhumdev.2011.10.005. Epub 2011 Nov 15.
- Background: PubMed 32380507Dani C, Coviello C, Montano S, Remaschi G, Petrolini C, Strozzi MC, Maggiora E, Sabatini M, Gazzolo D. Effect on splanchnic oxygenation of breast milk, fortified breast milk, and formula milk in preterm infants. Pediatr Res. 2021 Jan;89(1):171-174. doi: 10.1038/s41390-020-0935-1. Epub 2020 May 7.
- Background: PubMed 29369068Garvey AA, Dempsey EM. Applications of near infrared spectroscopy in the neonate. Curr Opin Pediatr. 2018 Apr;30(2):209-215. doi: 10.1097/MOP.0000000000000599.
- Individual participant dataSharing planned: No
Related trials for Gastric Residual Volume
Recruiting
Continuous Versus Intermittent Enteral Feeding and Gastric Residual Volume in Critically Ill Patients
Enteral Feeding Intolerance, Critical Illness
Recruiting
Effect of Prolonged Fasting Time on Gastric Residual Volume in Patients Taking GLP1 Receptor Agonists
Upper Endoscopy, GLP1-R-related Disease
Not yet recruitingObservational study
Preoperative Gastric Volume and High-Risk Gastric Content in Patients With Type 2 Diabetes Mellitus
Type 2 Diabetes Mellitus (DM), Gastric Ultrasound
Not yet recruitingObservational study
Effect of Resuscitation on Gastric Emptying Using POCUS in Pediatric Trauma Patients
Hemorrhagic Shock, Pediatric Trauma
RecruitingObservational study
Gastric Emptying and Enteral Nutrition Tolerance According to Vasopressor Dose in ICU Patients
Gastroparesis, Shock
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Prone, right lateral, and semi-elevated supine positions, Semi-elevated supine, prone, and right lateral positions and Right lateral, semi-elevated supine, and prone positions in people with Gastric Residual Volume and Abdominal Oxygenation, run by Istanbul University - Cerrahpasa at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 24 Jul 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Preterm newborn abdominal NIRS value (time frame: Preterm newborns whose feedings are every two hours will be monitored for 6 hours and those whose feedings are every three hours will be monitored for 9 hours. Preterm newborns will be monitored for a total of three feedings). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05888090, which also lists 23 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Jul 2025.