Clinical trials: Enteral Nutrition Feeding
Protein Feeding in Post-traumatic Injury Patients
Early and Adequate Protein Feeding Post-Traumatic Injury
A randomized, parallel-group, pilot study comparing the effect of the early addition of intravenous protein to enteral feeding as tolerated versus enteral feedings as tolerated alone immediately post traumatic injury.
- Trial name
- EMS (NCT02837861)
- Testing
- Routine Nutritional Support plus supplemental IV amino acids, Routine Nutritional Support
- Where
- United States
- Volunteers
- 45 people
- Sponsor
- Boston Medical Center
Acute Pancreatitis
Enteral Nutrition in Acute Pancreatitis
The purpose of this prospective randomised clinical trial is to compare beneficial and harmful effects of the use enteral nutrition versus a nil-by-mouth and intravenous fluid replacement principle of treatment in patients with…
- Trial name
- NCT01965873
- Testing
- Enteral nutrition
- Volunteers
- 214 people
- Sponsor
- University Hospital Rijeka
Enteral Nutrition, Enteral Nutrition Feeding
Stepwise Enteral Nutritional Algorithm and Patient Outcomes in Pediatric Intensive Care Units
The aim of the study to evaluate the effectiveness and patient's outcome after implementing enteral nutrition algorithm designed to achieve optimal enteral nutrition delivery in the pediatric intensive care unit and to evaluate…
- Conditions
- Enteral Nutrition, Enteral Nutrition Feeding, Enteral Nutrition Intolerance in Critically Ill Patients
- Trial name
- NCT07307027
- Testing
- Stepwise Enteral Nutritional Algorithm
- Where
- Egypt
- Volunteers
- 80 people
- Sponsor
- Ain Shams University
Intracerebral Hemorrhage
Effect of Intermittent Oro-esophageal Tube vs Nasogastric Tube in Tracheostomized Patients With Intracerebral Hemorrhage
This was a multicenter, prospective, randomized controlled clinical trail involved tracheostomized patients with Intracerebral Hemorrhage transferred to the Department of Rehabilitation Medicine of 4 hospitals in China between…
- Trial name
- NCT06203561
- Testing
- Basic treatment, comprehensive rehabilitation therapy, Intermittent Oro-esophageal Tube Feeding
- Where
- China
- Volunteers
- 118 people
- Sponsor
- Zeng Changhao
Gastroparesis
Evaluation of Single Doses of GSK962040 in Critically Ill Patients With Enteral Feed Intolerance
The aims of MOT112571 are to assess the pharmacodynamic effects, safety, tolerability, pharmacokinetics, and potential therapeutic benefit of single doses of GSK962040 in critically ill patients with delayed gastric emptying and…
- Trial name
- NCT01039805
- Testing
- GSK962040 (50 mg), GSK962040 (75 mg)
- Where
- Australia
- Volunteers
- 34 people
- Sponsor
- GlaxoSmithKline
Gastrointestinal Dysfunction, Critical Illness
Effect of Different Feeding Method on Gastrointestinal Function of Critical Patients
The intestine is the most vulnerable target organ in septic patients and is the first to be damaged organ in multiple organ dysfunction syndrome(MODS).Therefore, improving intestinal motility and mucosal barrier function is…
- Conditions
- Gastrointestinal Dysfunction, Critical Illness, Nutrition Disorders
- Trial name
- DFM-GFC (NCT04224883)
- Testing
- Continuously feeding, 16-hours feeding, intermittent feeding
- Where
- China
- Volunteers
- 90 people
- Sponsor
- Guangdong Provincial Hospital of Traditional Chinese Medicine
Surgical Resection of an Upper Gastrointestinal Malignancy, Nutritional Supplementation Via a Jejunostomy Post Discharge From Hospital
Enteral Feeding in Discharged Patients
Patients due to undergo surgery for oesophageal and gastric malignancy are often malnourished. Up to 10% of patients preoperative weight may also be lost during the early postoperative period.
- Trial name
- NCT02155140
- Testing
- Jejunal feeding
- Where
- United Kingdom
- Volunteers
- 45 people
- Sponsor
- University Hospital Plymouth NHS Trust
Complication
Comparative Study Between Two Routes of Enteral Feeding
The study assess, evaluate and compare the efficacy of two methods of enteral feeding on complications and nutritional status among ICU patients.
- Trial name
- NCT04576234
- Testing
- entral feeding
- Where
- Egypt
- Volunteers
- 60 people
- Sponsor
- Sarah Asmaa
Esophageal Cancer, Esophageal Carcinoma
Effect of Feeding Jejunostomy on Sarcopenia in Patients With Esophageal Cancer
Participants were diagnosed with esophageal cancer needing chemo- or radiochemotherapy before the potentially curing surgery consisting of esophagectomy.
- Conditions
- Esophageal Cancer, Esophageal Carcinoma, Sarcopenia, Feeding Tube
- Trial name
- NCT06712706
- Testing
- Feeding jejunostomy placement, Feeding jejunostomy placement at esophagectomy
- Where
- Switzerland
- Volunteers
- 60 people
- Sponsor
- Stefan Gutknecht
Gastrointestinal Tolerance
TolerUp Enteral Feeding Protocol
This prospective, observational, multi-center study will follow children with cerebral palsy who decided to switch to an enteral product that contains partially hydrolyzed protein and medium chain triglycerides as a result of…
- Trial name
- NCT03648255
- Where
- 19 sites in Turkey (Türkiye)
- Volunteers
- 133 people
- Sponsor
- Abbott Nutrition
Enteral Feeding Intolerance
The Effects of Bolus, Intermittent and Continuous Enteral Feeding on Blood Glucose and Feeding Intolerance in ICU Patients With Sepsis
Comparison of the effects of bolus, intermittent and continuous enteral feeding techniques on plasma glucose level and enteral feeding intolerance in adult intensive care unit patients with sepsis.
- Trial name
- NCT05812664
- Testing
- enteral feeding, blood glucose measurements, Evaluation of feeding intolerance with gastric residue
- Where
- Turkey (Türkiye)
- Volunteers
- 93 people
- Sponsor
- Umraniye Education and Research Hospital
Bottlefeeding, Infant, Premature, Diseases
Impact of Feeding Interval of Preterms on the Time of Transition From Tube Feeding to Oral Feeding
Preterms are usually fed with intervals of either two or three hours during their stay in neonatal intensive care unit. Recommendations of World Health Organization about feeding regimens, 3-hourly for infants 1500 - 2000 gr, and…
- Trial name
- NCT02916914
- Testing
- Q2 feeding
- Where
- Turkey (Türkiye)
- Volunteers
- 80 people
- Sponsor
- Etlik Zubeyde Hanim Womens' Health and Teaching Hospital
Prematurity, Lactose Intolerance
Lactase Enzyme Supplementation for Growth and Feeding Tolerance in Preterm Infants
Preterm infants commonly experience feeding intolerance, which can delay advancement of enteral feeding and impair early growth.
- Conditions
- Prematurity, Lactose Intolerance, Feeding Intolerance
- Trial name
- NCT07494123
- Testing
- Lactase Enzyme Supplementation
- Where
- Egypt
- Volunteers
- 124 people
- Sponsor
- Cairo University
Type 1 Diabetes Mellitus
Prematurity Prevalence Among T1D Patients and Its Characteristics Compared With Premature-born Non-diabetic Patients
The aims of this study are: 1. To assess the prevalence of prematurity, especially early prematurity, among T1D patients, and compare it to the prematurity prevalence among the non-diabetic general population in Israel. 2.
- Trial name
- T1Dpremies (NCT02929953)
- Testing
- chart review
- Where
- Israel
- Volunteers
- 3,600 people
- Sponsor
- Assaf Harofeh MC
Random Allocation, Intermittent Fasting
Pivotal BE Study of TAH3311 ODF vs ELIQUIS® Tablet Under Fasted Condition in Healthy Volunteers
This single-dose, open-label, randomized, four-way crossover study evaluates the pharmacokinetics, safety, and tolerability of TAH3311 5 mg in healthy volunteers under fasted and fed conditions.
- Conditions
- Random Allocation, Intermittent Fasting, Enteral Feeding
- Trial name
- NCT06689436
- Testing
- 5 mg Apixaban Oral Dissolving Film (fasting), 5 mg Apixaban Oral Dissolving Film (fed), 5 mg Apixaban Oral Tablet (US RS/RLD)
- Where
- United States
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- TAHO Pharmaceuticals Ltd.
Pain, Stress
The Effect of Feeding Positions During Tube Feeding on Stress, Pain Level and Feeding Tolerance of Preterm Infants
Premature infants have a need for an orogastric or nasogastric feeding tube because of the immaturity of coordination between suck-swallow and breathing. Tube feeding could cause feeding intolerance and stress.
- Conditions
- Pain, Stress, Enteral Feeding Intolerance
- Trial name
- NCT04156529
- Testing
- ESU position, ESRL position
- Where
- Turkey (Türkiye)
- Volunteers
- 34 people
- Sponsor
- Sibel Serap Ceylan
Full Enteral Nutrition, the Day and Night Cycle
The Effect of Day-Night Cycle on the Transition Time to Full Enteral Feeding in Preterm Newborns Receiving Oropharyngeal Colostrum
The aim of this study was to examine the effect of the day-night cycle on the transition time to full enteral nutrition in premature infants receiving oropharyngeal colostrum.
- Trial name
- PRETERM (NCT06883903)
- Testing
- day-night cycle application, routine practice
- Where
- Turkey (Türkiye)
- Volunteers
- 60 people
- Sponsor
- Biruni University
Esophageal Cancer
Design of the EFECTS Trial
It is well known that there is a considerable postoperative weight loss in patients undergoing esophageal resection for cancer. We believe that this weigh loss can be limited by administering postoperative enteral feeding…
- Trial name
- EFECTS (NCT02017366)
- Testing
- Enteral feeding
- Where
- Belgium
- Sponsor
- University Hospital, Gasthuisberg
Gastroesophageal Reflux
Effect of Tube Feeding on Gastroesophageal Reflux in Preterm Infants
Due to several promoting factors, gastro-esophageal reflux (GER) is very frequent in preterm infants. To limit the potentially harmful widespread of pharmacological treatment, a step-wise approach, which firstly undertakes…
- Trial name
- FT-GER-SO (NCT02837627)
- Testing
- Tube feeding
- Where
- 2 sites in Italy
- Volunteers
- 31 people
- Sponsor
- IRCCS Azienda Ospedaliero-Universitaria di Bologna
Acute Lung Injury
Intensive Nutrition in Acute Respiratory Distress Syndrome (ARDS): A Clinical Trial (INTACT)
The investigators propose a prospective randomized clinical trail to evaluate the impact of intensive medical nutrition therapy (IMNT) in patients with acute respiratory distress syndrome (ARDS) or acute lung injury (ALI) on…
- Trial name
- INTACT (NCT01921101)
- Testing
- intensive medical nutrition, control
- Where
- United States
- Volunteers
- 78 people
- Sponsor
- University of Illinois Chicago