Body CompositionCrescerNCT00875251
Growth and Body Composition in Preterm Infants
An observational study of Body Composition, run by Oswaldo Cruz Foundation at 2 sites in Brazil.
Trial summary
Growth is traditionally used as a prognostic measure after admission to a neonatal intensive care unit (NICU). Quality of neonatal intensive care is one of the factors determining the health and quality of life for those that survive, with the principal objective of increasing disability-free survival. Read more about this study
- Who is it for?
- Ages Up to 6 months
- Conditions the study is for
- Body Composition
- What is being tested?
- body composition
- Type of treatment
- Medical device
- How many people
- 60 participants
- Where
- 2 sitesBrazil
- Study dates
- 1 Apr 2009to 30 Dec 2021
- Phase
- Observational
- 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 Up to 6 months
- All sexes
- No healthy volunteers
- Child
Study population: Preterm infants with birth weight less than 1500g Term infants without IUGR
Who may be able to join
- appropriate for gestational age (AGA) and small for gestational age (SGA) premature newborns with gestational age less than or equal to 32 weeks and less than 1500g at birth
- AGA term newborns with gestational age greater than or equal to 37 weeks and less than 42 weeks and with no history of maternal disease that might compromise intrauterine growth
Who cannot join
- congenital malformations
- genetic syndromes confirmed by the geneticist
- clinically and laboratory-confirmed congenital infections
- children of mothers with the human immunodeficiency virus (HIV)
- children of diabetic mothers
- newborns that develop severe intraventricular hemorrhage or necrotizing enterocolitis
Trial locations and contacts
2 sites in 1 country.
Brazil2 sites, 2 recruiting
- Enrolling by invitation
Instituto Fernandes Figueira
Rio de Janeiro, Rio de Janeiro, 22520-040
- Recruiting
Maria Elisabeth L Moreira
Rio de Janeiro, 22420040
Maria E Moreira, MD, 552125132224, bebeth@iff.fiocruz.br
Dalva B Meio, MD
About this study
Official title: Growth and Body Composition of Very Low Birth Weight Infants Compared With Infants Birth at Term
Growth is traditionally used as a prognostic measure after admission to a neonatal intensive care unit (NICU). Quality of neonatal intensive care is one of the factors determining the health and quality of life for those that survive, with the principal objective of increasing disability-free survival. Nowadays, there is some researches showing us that these preterm babies present a different body composition when they achieve term age compared with babies birth at term and this condition could be putting these babies in risk to metabolic syndrome early in adult age. The majority of infants born between 24 and 29 weeks of gestational age fail to achieve the mean birth weight for fetuses of the same gestational age, and many weigh below the 10th percentile at hospital discharge. The focus of this study is the growth and body composition of very low birth weight infants growing in the extrauterine environment. The central question is, when they reach the corresponding term weight, is the body composition of newborns growing outside of the uterus different from that of infants growing in the intrauterine environment? The investigators are also trying to validate 3 different methods to research body composition: DXA, air-displacement plethysmography and electric bioimpedance.
Read the detailed description
OBJECTIVES
GENERAL:
Evaluate the growth and body composition of VLBW infants upon reaching the corresponding term gestational age (GA) and weight.
SPECIFIC:
- Evaluate the longitudinal growth and body composition of VLBW infants from the first week of life and at the corresponding term GA and weight.
- Relate the weight loss in the first week of life to the weight and percentage of total body water at the corresponding term GA and weight.
- Compare the body composition of VLBW newborns growing in the extrauterine environment upon reaching the corresponding term GA and weight with the body composition of term newborns, using the 3 methods (DEXA, air-displacement plethysmography, and electric bioimpedance) D) Adjust a predictive model for body weight estimates using the parameters furnished by multi-frequency and single-frequency electric bioimpedance and anthropometry, with the measurements provided by DEXA and plethysmography as the gold standard.
- Relate body weight and composition at the corresponding term GA to neonatal morbidity.
METHODOLOGY Study characteristics A mixed longitudinal study will be conducted. The newborns will be included at different gestational ages and will remain in the study until reaching the corresponding term gestational age and weight (2,800g to 3,200g).
Study site The study will be performed at the Fernandes Figueira Institute (IFF), a unit of the Oswaldo Cruz Foundation in Rio de Janeiro, Brazil.
Study population The study population will consist of premature newborns with gestational age less than 32 weeks and/or with intrauterine growth restriction. Data will be collected beginning at birth during hospitalization and in the outpatient follow-up after hospital discharge.
Definitions and established criteria
Evaluation of the adequacy of weight in relation to gestational age was based on the curve by Alexander et al. (1996), defining SGA as newborns with birth weight below the 10th percentile in relation to gestational age; AGA was defined as between the 10th and 90th percentiles; and large for gestational age (LGA) as above the 90th percentile.
Intrauterine growth restriction (IUGR) This study defines IUGR as a Z-score for the newborn's birth weight for gestational age less than or equal to -2. The study will use the sex-specific Canadian reference for birth weight for gestational age, which uses the 3rd, 5th, 10th, 50th (mean), 90th, 95th, and 97th percentiles for 22 to 43 complete weeks and standard deviation (Kramer et al, 2001).
Z-score. The measurements to be used with references for obtaining the Z-score will be those of Fenton et al.
Gestational age Gestational age will be based on the mother's date of last menstrual period. In case of doubt, confirmation will be obtained by the date of gestational age estimated by first-trimester ultrasound or, if necessary, by the Ballard method (Ballard et al, 1991), which estimates gestational age based on the newborn's somatic characteristics and neurological evaluation.
Corrected gestational age After obtaining gestational age at birth, age will be corrected over the course of the study by adding the weeks of post-natal life. Each age in weeks will consider the variation from zero to six days.
Morbidities
- Bronchopulmonary dysplasia will be defined as any newborn in use of oxygen therapy at 36 weeks corrected gestational age.
- Late-onset sepsis will be defined as a positive blood or CSF culture in the presence of clinical signs of sepsis after 72 hours of life or clinical infection with a negative culture after 72 hours of life for newborns that have received 5 or more days of antibiotic therapy.
- Necrotizing enterocolitis will be considered when classified as stage II A or higher according to the modified Bell criteria (Walsh \& Kleigman, 1986).
- Severe intraventricular hemorrhage will be defined as grade 3 or 4 according to the scale described by Papile et al (1978).
Measurements of body weight, length, foot size, triceps skinfold, mid-arm circumference, and total body water will be taken at 5 moments in the premature infants: in the first 24 hours of life, at the 7th day of life after recovering birth weight, at term (GA ≥ 37 < 42 weeks), and with weight from 2,800 to 3,200g. The two latter measurements may be taken after hospital discharge, during outpatient follow-up. These variables will be evaluated in the first 24 hours of life in the term newborns with weight from 2,800g to 3,200g.
Anthropometric Evaluation Measurements will be performed by the researcher, following previous training, considering the mean of the three measurements. The newborn will be measured unclothed and kept under previously prescribed heating, except during weighing.
Weight Weight will be measured with a Filizola brand digital scale accurate to 5 grams, after taring it before each weighing.
Length Length will be measured using an anthropometric ruler designed and manufactured at the precision workshop of the University of São Paulo in Ribeirão Preto, São Paulo State.
The newborn will be placed in the supine position on a flat surface as stiff as possible, adjusting the child's head in a medial position on the ruler's fixed surface. Holding the child in this position with the knees extended by an assistant, the ruler's mobile extremity will be moved until the ruler is perfectly adjusted to the soles of the newborn's feet.
Head circumference Head circumference will be measured using a non-elastic tape measure marked in millimeters. The tape measure will be adjusted to the newborn's head, passing in front across the supra-orbital region, above the eyebrows, and behind across the occipital bulge, recording the largest circumference obtained.
Foot size The measurement is taken with a caliper marked in millimeters, adjusting it to the largest diameter of the infant's right foot.
Triceps Skinfold (TSF) Triceps skinfold measurements will be taken with a Harpenden type caliper, which measures in millimeters, accurate to 0.1mm.
This measurement will always be taken on the right arm, at the midpoint between the acromion and the olecranon, immediately below the skin hollow, with the arm extended. The measurement recorded will be that obtained after stabilizing the caliper pointers (approximately 60 seconds).
Mid-arm circumference (MAC) This circumference will be obtained, always from the left arm, at the midpoint between the acromion and the olecranon, just below the skin hollow, with the arm extended and the hand in prone position, with a non-elastic millimeter tape measure (Sasanow et al, 1986). The location is the same as that of the triceps skinfold.
Mid-arm muscle circumference (MAMC) This parameter aims to measure the arm's muscle size and thus indirectly indicate the newborn's nutritional status during extrauterine growth. It uses 2 combined measurements, the triceps skinfold and the mid-arm circumference.
Body composition evaluation Body composition will be evaluated using the 3 methods available at the Fernandes Figueira Institute (BIA, plethysmography, and DEXA). The study will measure total body water, lean mass, and body fat.
Bioimpedance measurements will be made with the RJL System (Quantum BIA 101Q equipment) and the Hydra multi-frequency equipment (Xitron technologies) . Both pieces of equipment are inexpensive and the tests are non-invasive and can be performed at bedside. However, neither of them is validated for measuring body fat in newborns and infants (first year of life).
We will use quadripolar electrodes preferably on the right hand and foot. The electrodes are cut in ± 1 cm strips and attached to the hand and foot with a minimum distance of 3 cm between them (wrist and ankle flexure and immediately before the base of the fingers and toes). The anatomical criterion for positioning the electrodes was chosen based on the fact that the study focuses on human beings during their growth process, which can double or triple the birth weight during the study period. The newborns are measured before feeding, in prone position, wearing dry disposable diapers. The arms are kept away from the trunk and the legs should not touch each other. The infant should be comfortable and quiet, and the measurements should be recorded when the variation is no greater than ± 1 point. The difference in the resistance values obtained between the distal positions (right hand and right foot, right hand and left foot, left hand and left foot, and left hand and right foot) is not significant, and the electrodes can thus be used in these positions.
The equations used to calculate total body water (TBW) will be those proposed and validated by Tang Wing et al in 1997, which use 2 anthropometric measurements (weight and foot length) and resistance (R) measured by the electric bioimpedance technique.
Body fat percentage and total body composition will be measured by the air-displacement plethysmography in the PEA POD System and in the iDEXA equipment, using the software for small animals. Based on these measurements of real body fat, predictive models will be adjusted to estimate body fat using the parameters obtained from bioimpedance (resistance and reactance) and anthropometry (Hull et al, 2008, Roggero et al, 2008, Ellis et al, 2008, Ma et al, 2008).
Statistical analysis Data analysis will use Epi Info (Epi - 6.04) from the Centers for Disease Control (CDC - Atlanta, USA).
We will use analysis of variance for continuous variables with normal distribution and non-parametric Kruskal-Wallis tests for the others to analyze differences between the groups. The chi-square test will be used for the categorical variables to calculate the difference in proportions. A frequency table will be used for the categorical variables and the mean or median and standard deviation for the continuous variables.
The models for estimating body fat based on bioimpedance measurements will be fitted using multiple linear regression models.
- Conditions
- Body Composition
- Being tested
- body composition
- Keywords
- body composition, preterm infant, anthropometry
- Medical subject headings
- Premature Birth
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
body compositionDevice
Also called air displacement plethysmography
Measurements of body composition using 2 differents devices: Bioimpedance measurements will be made with the RJL System (Quantum BIA 101Q equipment) air-displacement plethysmography in the PEA POD System (Life Measurement).
| Study group | Role | What they receive |
|---|---|---|
| term infants body composition | Term infants from 2 days of life to 7 days of life without IUGR Receives: Device: body composition | |
| preterm infants body composition | very low birth weight infants before discharge Receives: Device: body composition |
What is being measured
The primary outcome is the main question the study is designed to answer.
body composition
fat mass and fat free mass from PEA BOD
Measured: from discharge to 3 months of chronological age
Secondary outcomes (1)
anthropometry
Anthropometry assesment : weight, lenght, head circunference, skinfold thikness, BMI
Measured: from term to first year of life
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted3 Apr 2009 (estimated)
- Study start1 Apr 2009
- Primary completion30 Dec 2021 (estimated)
- Study completion30 Dec 2021 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Body CompositionStudies of the same condition, open and under way.
- 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
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 60 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Oswaldo Cruz Foundation
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Maria Elisabeth Lopes Moreira, Oswaldo Cruz Foundation
- Investigators
- Maria E Moreira, MD, Principal investigator, Oswaldo Cruz Foundation
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00875251
- Sponsor's protocol ID
- CAAE - 0292.0.008.000-05
- Acronym
- Crescer
- Status last verified
- Sep 2020
- First submitted
- 2 Apr 2009
- Last updated
- 18 Sep 2020
- Results posted
- No
- Data monitoring committee
- Yes
Publications
Nehab SR, Villela LD, Soares FVM, Abranches AD, Araujo DMR, da Silva LML, Amaral YNV, Junior SCG, Meio MDBB, Moreira ME. Gestational weight gain and body composition of full-term newborns and infants: a cohort study. BMC Pregnancy Childbirth. 2020 Aug 20;20(1):474. doi: 10.1186/s12884-020-03145-x.
PubMed 32819310
Study at a glance
From the registry record, last updated by the sponsor on 18 Sep 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Growth and Body Composition of Very Low Birth Weight Infants Compared With Infants Birth at Term
- ClinicalTrials.gov ID
- NCT00875251
- Acronym / sponsor ID
- Crescer / CAAE - 0292.0.008.000-05
- Conditions
- Body Composition
- Keywords
- body composition, preterm infant, anthropometry
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 60 participants (estimated)
- Lead sponsor
- Oswaldo Cruz FoundationUniversity, hospital or other
- Study start
- 1 Apr 2009 (actual)
- Primary completion
- 30 Dec 2021 (estimated)
- Study completion
- 30 Dec 2021 (estimated)
- First posted
- 3 Apr 2009 (estimated)
- 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.
Growth is traditionally used as a prognostic measure after admission to a neonatal intensive care unit (NICU). Quality of neonatal intensive care is one of the factors determining the health and quality of life for those that survive, with the principal objective of increasing disability-free survival. Nowadays, there is some researches showing us that these preterm babies present a different body composition when they achieve term age compared with babies birth at term and this condition could be putting these babies in risk to metabolic syndrome early in adult age. The majority of infants born between 24 and 29 weeks of gestational age fail to achieve the mean birth weight for fetuses of the same gestational age, and many weigh below the 10th percentile at hospital discharge. The focus of this study is the growth and body composition of very low birth weight infants growing in the extrauterine environment. The central question is, when they reach the corresponding term weight, is the body composition of newborns growing outside of the uterus different from that of infants growing in the intrauterine environment? The investigators are also trying to validate 3 different methods to research body composition: DXA, air-displacement plethysmography and electric bioimpedance.
Detailed description
OBJECTIVES
GENERAL:
Evaluate the growth and body composition of VLBW infants upon reaching the corresponding term gestational age (GA) and weight.
SPECIFIC:
- Evaluate the longitudinal growth and body composition of VLBW infants from the first week of life and at the corresponding term GA and weight.
- Relate the weight loss in the first week of life to the weight and percentage of total body water at the corresponding term GA and weight.
- Compare the body composition of VLBW newborns growing in the extrauterine environment upon reaching the corresponding term GA and weight with the body composition of term newborns, using the 3 methods (DEXA, air-displacement plethysmography, and electric bioimpedance) D) Adjust a predictive model for body weight estimates using the parameters furnished by multi-frequency and single-frequency electric bioimpedance and anthropometry, with the measurements provided by DEXA and plethysmography as the gold standard.
- Relate body weight and composition at the corresponding term GA to neonatal morbidity.
METHODOLOGY Study characteristics A mixed longitudinal study will be conducted. The newborns will be included at different gestational ages and will remain in the study until reaching the corresponding term gestational age and weight (2,800g to 3,200g).
Study site The study will be performed at the Fernandes Figueira Institute (IFF), a unit of the Oswaldo Cruz Foundation in Rio de Janeiro, Brazil.
Study population The study population will consist of premature newborns with gestational age less than 32 weeks and/or with intrauterine growth restriction. Data will be collected beginning at birth during hospitalization and in the outpatient follow-up after hospital discharge.
Definitions and established criteria
Evaluation of the adequacy of weight in relation to gestational age was based on the curve by Alexander et al. (1996), defining SGA as newborns with birth weight below the 10th percentile in relation to gestational age; AGA was defined as between the 10th and 90th percentiles; and large for gestational age (LGA) as above the 90th percentile.
Intrauterine growth restriction (IUGR) This study defines IUGR as a Z-score for the newborn's birth weight for gestational age less than or equal to -2. The study will use the sex-specific Canadian reference for birth weight for gestational age, which uses the 3rd, 5th, 10th, 50th (mean), 90th, 95th, and 97th percentiles for 22 to 43 complete weeks and standard deviation (Kramer et al, 2001).
Z-score. The measurements to be used with references for obtaining the Z-score will be those of Fenton et al.
Gestational age Gestational age will be based on the mother's date of last menstrual period. In case of doubt, confirmation will be obtained by the date of gestational age estimated by first-trimester ultrasound or, if necessary, by the Ballard method (Ballard et al, 1991), which estimates gestational age based on the newborn's somatic characteristics and neurological evaluation.
Corrected gestational age After obtaining gestational age at birth, age will be corrected over the course of the study by adding the weeks of post-natal life. Each age in weeks will consider the variation from zero to six days.
Morbidities
- Bronchopulmonary dysplasia will be defined as any newborn in use of oxygen therapy at 36 weeks corrected gestational age.
- Late-onset sepsis will be defined as a positive blood or CSF culture in the presence of clinical signs of sepsis after 72 hours of life or clinical infection with a negative culture after 72 hours of life for newborns that have received 5 or more days of antibiotic therapy.
- Necrotizing enterocolitis will be considered when classified as stage II A or higher according to the modified Bell criteria (Walsh \& Kleigman, 1986).
- Severe intraventricular hemorrhage will be defined as grade 3 or 4 according to the scale described by Papile et al (1978).
Measurements of body weight, length, foot size, triceps skinfold, mid-arm circumference, and total body water will be taken at 5 moments in the premature infants: in the first 24 hours of life, at the 7th day of life after recovering birth weight, at term (GA ≥ 37 < 42 weeks), and with weight from 2,800 to 3,200g. The two latter measurements may be taken after hospital discharge, during outpatient follow-up. These variables will be evaluated in the first 24 hours of life in the term newborns with weight from 2,800g to 3,200g.
Anthropometric Evaluation Measurements will be performed by the researcher, following previous training, considering the mean of the three measurements. The newborn will be measured unclothed and kept under previously prescribed heating, except during weighing.
Weight Weight will be measured with a Filizola brand digital scale accurate to 5 grams, after taring it before each weighing.
Length Length will be measured using an anthropometric ruler designed and manufactured at the precision workshop of the University of São Paulo in Ribeirão Preto, São Paulo State.
The newborn will be placed in the supine position on a flat surface as stiff as possible, adjusting the child's head in a medial position on the ruler's fixed surface. Holding the child in this position with the knees extended by an assistant, the ruler's mobile extremity will be moved until the ruler is perfectly adjusted to the soles of the newborn's feet.
Head circumference Head circumference will be measured using a non-elastic tape measure marked in millimeters. The tape measure will be adjusted to the newborn's head, passing in front across the supra-orbital region, above the eyebrows, and behind across the occipital bulge, recording the largest circumference obtained.
Foot size The measurement is taken with a caliper marked in millimeters, adjusting it to the largest diameter of the infant's right foot.
Triceps Skinfold (TSF) Triceps skinfold measurements will be taken with a Harpenden type caliper, which measures in millimeters, accurate to 0.1mm.
This measurement will always be taken on the right arm, at the midpoint between the acromion and the olecranon, immediately below the skin hollow, with the arm extended. The measurement recorded will be that obtained after stabilizing the caliper pointers (approximately 60 seconds).
Mid-arm circumference (MAC) This circumference will be obtained, always from the left arm, at the midpoint between the acromion and the olecranon, just below the skin hollow, with the arm extended and the hand in prone position, with a non-elastic millimeter tape measure (Sasanow et al, 1986). The location is the same as that of the triceps skinfold.
Mid-arm muscle circumference (MAMC) This parameter aims to measure the arm's muscle size and thus indirectly indicate the newborn's nutritional status during extrauterine growth. It uses 2 combined measurements, the triceps skinfold and the mid-arm circumference.
Body composition evaluation Body composition will be evaluated using the 3 methods available at the Fernandes Figueira Institute (BIA, plethysmography, and DEXA). The study will measure total body water, lean mass, and body fat.
Bioimpedance measurements will be made with the RJL System (Quantum BIA 101Q equipment) and the Hydra multi-frequency equipment (Xitron technologies) . Both pieces of equipment are inexpensive and the tests are non-invasive and can be performed at bedside. However, neither of them is validated for measuring body fat in newborns and infants (first year of life).
We will use quadripolar electrodes preferably on the right hand and foot. The electrodes are cut in ± 1 cm strips and attached to the hand and foot with a minimum distance of 3 cm between them (wrist and ankle flexure and immediately before the base of the fingers and toes). The anatomical criterion for positioning the electrodes was chosen based on the fact that the study focuses on human beings during their growth process, which can double or triple the birth weight during the study period. The newborns are measured before feeding, in prone position, wearing dry disposable diapers. The arms are kept away from the trunk and the legs should not touch each other. The infant should be comfortable and quiet, and the measurements should be recorded when the variation is no greater than ± 1 point. The difference in the resistance values obtained between the distal positions (right hand and right foot, right hand and left foot, left hand and left foot, and left hand and right foot) is not significant, and the electrodes can thus be used in these positions.
The equations used to calculate total body water (TBW) will be those proposed and validated by Tang Wing et al in 1997, which use 2 anthropometric measurements (weight and foot length) and resistance (R) measured by the electric bioimpedance technique.
Body fat percentage and total body composition will be measured by the air-displacement plethysmography in the PEA POD System and in the iDEXA equipment, using the software for small animals. Based on these measurements of real body fat, predictive models will be adjusted to estimate body fat using the parameters obtained from bioimpedance (resistance and reactance) and anthropometry (Hull et al, 2008, Roggero et al, 2008, Ellis et al, 2008, Ma et al, 2008).
Statistical analysis Data analysis will use Epi Info (Epi - 6.04) from the Centers for Disease Control (CDC - Atlanta, USA).
We will use analysis of variance for continuous variables with normal distribution and non-parametric Kruskal-Wallis tests for the others to analyze differences between the groups. The chi-square test will be used for the categorical variables to calculate the difference in proportions. A frequency table will be used for the categorical variables and the mean or median and standard deviation for the continuous variables.
The models for estimating body fat based on bioimpedance measurements will be fitted using multiple linear regression models.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| term infants body composition | – | Device: body compositionTerm infants from 2 days of life to 7 days of life without IUGR |
| preterm infants body composition | – | Device: body compositionvery low birth weight infants before discharge |
Who may qualify
- Ages
- Up to 6 months
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
- Study population
- Preterm infants with birth weight less than 1500g Term infants without IUGR
Key inclusion criteria (2 listed)
- appropriate for gestational age (AGA) and small for gestational age (SGA) premature newborns with gestational age less than or equal to 32 weeks and less than 1500g at birth
- AGA term newborns with gestational age greater than or equal to 37 weeks and less than 42 weeks and with no history of maternal disease that might compromise intrauterine growth
Key exclusion criteria (6 listed)
- congenital malformations
- genetic syndromes confirmed by the geneticist
- clinically and laboratory-confirmed congenital infections
- children of mothers with the human immunodeficiency virus (HIV)
- children of diabetic mothers
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 |
|---|---|---|
| body compositionAlso: air displacement plethysmographyMeasurements of body composition using 2 differents devices: Bioimpedance measurements will be made with the RJL System (Quantum BIA 101Q equipment) air-displacement plethysmography in the PEA POD System (Life Measurement). | Device | preterm infants body composition, term infants body composition |
Primary outcome
body composition
Time frame: from discharge to 3 months of chronological age
fat mass and fat free mass from PEA BOD
1 secondary outcome
anthropometry
Time frame: from term to first year of life
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 Sep 2020.
- Derived from this study: PubMed 32819310Nehab SR, Villela LD, Soares FVM, Abranches AD, Araujo DMR, da Silva LML, Amaral YNV, Junior SCG, Meio MDBB, Moreira ME. Gestational weight gain and body composition of full-term newborns and infants: a cohort study. BMC Pregnancy Childbirth. 2020 Aug 20;20(1):474. doi: 10.1186/s12884-020-03145-x.
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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.
Maria E Moreira, MD principal investigator
Oswaldo Cruz Foundation
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Body Composition, run by Oswaldo Cruz Foundation at 2 sites in Brazil.
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 2 inclusion and 6 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: status not confirmed, as of the sponsor's last update on 18 Sep 2020. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in Brazil. 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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Maria E Moreira, MD; PhD (55-21-25541911, bebeth@iff.fiocruz.br), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
body composition (time frame: from discharge to 3 months of chronological age). 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 NCT00875251, which also lists 1 linked publication.
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 18 Sep 2020.