Nutrition Disorders

8

Review clinical trials related to Nutrition Disorders. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

The Effect of the Distance of the Percutaneous Endoscopic Gastrostomy (PEG) Feeding Tube to the Pylorus on the Postoperative Outcomes

Nutrition is the intake of essential nutrients in sufficient quantities and at the appropriate times to maintain and improve health and enhance quality of life. Enteral nutrition is superior to parenteral nutrition and should be preferred. To protect the gastrointestinal mucosa and maintain normal flora, patients should begin enteral nutrition as soon as possible. In patients who cannot take food orally, enteral nutrition is provided via a nasogastric/nasojejunal tube or gastrostomy tube. Gastrostomy is the first choice for patients with a functional gastrointestinal system, poor oral intake, and requiring long-term nutritional support. Feeding tubes can be placed percutaneously or surgically. Percutaneous endoscopic gastrostomy (PEG) is a minimally invasive procedure that does not increase morbidity or mortality, is cheaper, and saves time compared to surgical gastrostomy. It was first applied in 1980 as an alternative to surgical gastrostomy. During the procedure, a line was defined between the navel and the middle of the left lower costal margin. A feeding tube was then inserted at the junction of the middle 2/3 and the outer 1/3 under local anesthesia, and feeding was started the following day. Vudayagiri et al. reported that the placement site is generally 2 cm medial to the costal margin and 2 cm below the xiphoid process. Different methods for placing a PEG tube into the stomach (pull technique, push technique, and Russell method) have been described in the literature, with the most common being the "pull" technique. The 2005 ESPEN guidelines noted that in the "pull" technique, gastroscopic visualization of the anterior gastric wall is performed, followed by determination of the puncture site at the distal corpus level. The exact location of the PEG feeding tube, both on the skin and within the gastric lumen, is not fully understood. Its localization on the abdominal skin will be optimally achieved through endoscopic transillumination. However, its level within the gastric lumen is predictable. In our study, we aimed to investigate how measuring the distance of the feeding tube from the pylorus in patients undergoing PEG placement affects post-procedure outcomes and to determine the optimal level within the gastric lumen. Additionally, the placement of the catheter on the skin will be recorded in each patient. Traditionally, tube feeding has been delayed until up to 24 hours after percutaneous endoscopic gastrostomy (PEG) procedure. However, results from various randomized controlled trials suggest that early feeding may be an option. A meta-analysis indicated that early feeding (\< or = 4 hours) after PEG placement may be a safe alternative to delayed or next-day feeding. However, although there was no difference in overall complications in this meta-analysis, there was a significant increase in gastric residual volume on day 1 in patients who started early feeding. In another meta-analysis conducted by Szary et al., early tube feeding ≤3 hours after PEG placement; Complications, death within ≤72 hours, or significant gastric residual volume on day 1 were found to be significantly different from delayed or next-day feeding. Our study will be the first of its kind in this field. Therefore, to minimize all factors that could negatively affect the results, we will initiate enteral feeding 24 hours after the traditionally used procedure.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Sisli Hamidiye Etfal Training and Research HospitalUpdated: Jun 18, 2026Duration: 7 Days
Eligibility criteria

Over 18 years of age [+3]

History of stomach, small intestine, large intestine surgery or any history of m... [+4]

Status: Recruiting

A Study of PF-08653945 and PF-08653944 in Adults With Overweight or Obesity (SOLIS-1)

This study is being done to learn about the safety and effects of the study drugs, PF-08653945 and PF-08653944, when given alone or together for weight loss, compared to a placebo (a dummy drug that has no active ingredient in it).

Participants needed: 872
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: PfizerUpdated: Jun 10, 2026Locations: 48
Eligibility criteria

adults aged 18 years or older with [+2]

Status: Recruiting

Nutritional Course of Care After Surgical Treatment at the Patients Affected by a Cancer of the Head and by the Neck

Whatever are the strategies of coverage, the consideration of the state of bad nutrition is not often the priority. According to the last recommendations (2012) of the French Society Clinical Nutrition and Metabolism (SFNEP), the surgeries of the cancers of the VADS are not listed among surgeries with high morbidity. So the specific recommendations for the patients undernourished with surgery with low morbidity, only a personalized dietary advice and oral nutritional supplements are recommended in preoperative. There is no specific recommendation in post-operative. Two groups of cancer patients of the VADS will be compared: a control group benefiting from a nutritional coverage based on the current recommendations of the SFNEP, an experimental group benefiting from an improved nutritional coverage. In preoperative, all the patients of experimental group will benefit from dietary advice during a multidisciplinary specific consultation. In post-operative, a dietetic consultation will be set up in 7 days at the exit of hospitalization and call phone at M1, M2, M4 and M5. And for the undernourished patient will benefit a multidisciplinary consultation at the rate of a consultation a month during 6 months. In the Group control, the patients will be followed according to the current recommendations of the SFNEP.

Participants needed: 60
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Centre Hospitalier Universitaire, AmiensUpdated: May 13, 2026Locations: 1
Eligibility criteria

Patients affected by a cancer of the VADS [+4]

Patient minor [+3]

Status: Recruiting

Replacing Protein Via Enteral Nutrition in Critically Ill Patients

The investigator will investigate the effect of supplemental enteral protein (1.2 g/kg/day) added to standard formula to achieve high amount of enteral protein (range 2-2.4 g/kg/day) given from ICU day 5 until ICU discharge up to ICU day 90 as compared to no supplemental enteral protein to achieve moderate amount enteral protein (0.8-1.2 g/kg/day), given in conjunction with similar amounts of stepwise caloric administration in the two groups on all-cause 90-day mortality.

Participants needed: 2,502
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: King Abdullah International Medical Research CenterUpdated: Sep 8, 2025Locations: 2
Eligibility criteria

Age ≥18-years old [+2]

Lack of commitment to full life support or brain death. Patients with "Do Not Re... [+9]

Status: Not yet recruiting

Semi-elemental Versus Polymeric EEN in the Preoperative Optimization for Patients with CD

Growing evidence has shown that exclusive enteral nutrition (EEN) plays an important role in the preoperative optimization for patients with Crohn's disease (CD). However, the efficacy and safety of different types of enteral feeds including semi-elemental and polymeric enteral nutrition on CD have not been investigated. The aim of this study was to compare the role of semi-elemental and polymeric enteral nutrition on CD.

Participants needed: 304
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Wei ZhouUpdated: Sep 19, 2024Locations: 1
Eligibility criteria

elective bowel resection for Crohn's disease; [+5]

emergency surgery; [+7]

Status: Recruiting

In-Person Lifestyle Program for Black Adolescent Girls at Risk for Type 2 Diabetes

The aim of this study is to look at changes in diabetes-related risk factors in Black adolescent girls who are at risk for type 2 diabetes and their primary female caregiver after both participating in a 12-week in-person lifestyle program.

Participants needed: 60
Trial details
Age: 12-18Biological sex: FemaleType: InterventionalSponsor: Cornell UniversityUpdated: Aug 16, 2024Locations: 1
Eligibility criteria

12-18 years of age [+2]

pregnant or within 3 months postpartum. [+11]

Status: Not yet recruiting

Effect of Nutritional Intervention Based on Prediction Model on Adult Umbilical Cord Blood Transplantation Patients

Based on the nutritional factor prediction model, the individualized nutritional management of patients with umbilical cord blood transplantation (UCBT) was carried out to observe the impact on the survival efficacy of patients.

Participants needed: 67
Trial details
Phase: Phase 2Age: 18-65Biological sex: AllType: InterventionalSponsor: Anhui Provincial HospitalUpdated: Aug 14, 2024Locations: 1
Eligibility criteria

Age 18-65 years old, conscious, with language communication skills; [+3]

Age < 18 years old or > 65 years old or with cognitive impairment can not comple... [+4]

Status: Recruiting

Nutrition Impact on Immunotherapy of Cancer

This study investigates nutritional status and outcomes of immuntherapy in cancer patients.

Participants needed: 300
Trial details
Phase: Phase 3Age: 18-80Biological sex: AllType: InterventionalSponsor: Qingdao Central HospitalUpdated: Jul 15, 2024Locations: 1
Eligibility criteria

Diagnosis of cancer, malnutrition Age >18 years Performance status ECOG of 0 or...

Patients unable to swallow orally administered medication and patients with Impa...