Clinical trials: Gastrostomy
Enteral Nutrition (Food for Special Medical Purposes), Enteral Feeds
A Single Arm Intervention Study to Assess the Acceptability, Tolerance and Ease of Use of Wilbo's Blends+ (Commercial Enteral Feed Based on Real Food) When Used as Part of a Dietitian Prescribed Enteral Feeding Plan
The goal of this observational study is to learn if tube-fed children and young people (age 3-15 years) find Wilbo's Blends+ (a new nutritionally complete enteral formula containing real food ingredients) acceptable, tolerable…
- Conditions
- Enteral Nutrition (Food for Special Medical Purposes), Enteral Feeds, Enteral Tube Nutrition, Gastrostomy Tube
- Trial name
- Wilbo's Blends (NCT07036081)
- Testing
- Wilbo's Blends+
- Where
- United Kingdom
- Volunteers
- 45 people
- Sponsor
- Nottingham University Hospitals NHS Trust
Nutritional Deficiency, Neuro-Degenerative Disease
Nutritional Prognostic Factors in ALS
Background. Several nutritional factors have been evaluated as prognostic factors for survival in ALS patients at earlier stages of the disease [body mass index (BMI), body composition expressed as fat free mass (FFM), fat mass…
- Conditions
- Nutritional Deficiency, Neuro-Degenerative Disease, Gastrostomy
- Trial name
- PEG-ALS (NCT03487536)
- Testing
- Nutritional assessment
- Where
- Italy
- Volunteers
- 47 people
- Sponsor
- University of Bari
Gastrostomy Complications
LASER THERAPY IN GASTRIC STOMA INJURIES OF CHILDREN AND ADOLESCENTS
Compare the healing time of lesions in the mucosa of the gastric stoma of children and adolescents using laser therapy versus conventional treatment with protective barrier powder.
- Trial name
- NCT04863196
- Testing
- Laser therapy Treatment Group, Barrier Dust Treatment Group
- Where
- Brazil
- Volunteers
- 70 people
- Sponsor
- University of Sao Paulo General Hospital
Feeding Difficulties, Gastrostomy
The Use of High Bile-Binding Foods to Reduce Upper Gastrointestinal Bile Acid Concentrations (Aim 3)
Using a longitudinal cohort design, we will compare the impact of a high BA-binding blenderized diet compared to a low BA-binding blenderized diet and an amino acid-based formula, on gastrointestinal and pulmonary hospitalization…
- Conditions
- Feeding Difficulties, Gastrostomy, Aspiration
- Trial name
- NCT06913621
- Testing
- amino acid formula, low bile acid binding blenderized diet, high bile acid binding blenderized diet
- Volunteers
- 138 people
- Sponsor
- Boston Children's Hospital
Gastrostomy Complications
Clinical Trial of Gastrostomy Button Securement Device
Gastrostomy button (G-button) complications, such as granulation tissue formation, tube dislodgements, leakage, skin irritation or infection are frequent causes of post-operative clinic and emergency department visits.
- Trial name
- NCT04001946
- Testing
- Button Huggie
- Where
- 4 sites in United States
- Volunteers
- 182 people
- Sponsor
- University of Colorado, Denver
Gastrostomy
Predictive Factors for Roux Stasis Syndrome
Patients who were pathologically diagnosed with gastric cancer and underwent distal gastrectomy with R-Y reconstruction between March 2014 and March 2021 were retrospectively analyzed.
- Trial name
- PFRSS (NCT04919577)
- Testing
- X-ray
- Where
- China
- Volunteers
- 220 people
- Sponsor
- Peking University Third Hospital
Feeding and Eating Disorders of Childhood, Enteral Nutrition Dependence
Gut Microbiota Changes in Children Receiving Exclusive Enteral Nutrition With Compleat® Paediatric
This observational, prospective, single-center study aims to evaluate changes in the fecal microbiota of pediatric patients receiving exclusive enteral nutrition following the introduction of Compleat® Paediatric Nature Mix, an…
- Trial name
- COMPLEAT (NCT07816536)
- Where
- France
- Volunteers
- 8 people
- Sponsor
- Establishment for Children and Adolescents in the Nantes Region
Gastrostomy
The Quality of Life of Children With Gastrostomy
Study the quality of life with generic questionnaires (17-20), validated and used in other pathologies and chronic diseases of the child.
- Trial name
- NCT04016519
- Testing
- Gastrostomie
- Where
- France
- Volunteers
- 200 people
- Sponsor
- Assistance Publique Hopitaux De Marseille
Gastrostomy, Gastrostomy Complications
Pediatric Percutaneous Ultrasound Gastrostomy Technique
The purpose of this research study is to test a new device called the PUMA-G Pediatric System. The research will measure if the device works well to safely aid doctors placing gastrostomy feeding tubes in children.
- Conditions
- Gastrostomy, Gastrostomy Complications, Pediatric Disorder, Ultrasound
- Trial name
- NCT05966311
- Testing
- Percutaneous Ultrasound Gastrostomy
- Where
- 3 sites in United States
- Volunteers
- 80 people
- Sponsor
- CoapTech
Feeding and Eating Disorders of Childhood, Gastrostomy
CHAMP App Feeding Difficulties Repository
This repository will consist of home monitoring data, videos, and images of patients with feeding difficulties for asynchronous remote patient monitoring of manually entered data sent by parents to the healthcare team using the…
- Conditions
- Feeding and Eating Disorders of Childhood, Gastrostomy, Feeding Disorder of Infancy and Childhood
- Trial name
- NCT06129877
- Testing
- CHAMP App
- Where
- United States
- Volunteers
- 1,000 people
- Sponsor
- Children's Mercy Hospital Kansas City
Postprocedural Delayed Gastric Emptying
The Effect of Elemental Diet on Gastric Emptying
In patients with percutaneous endoscopic gastrostomy (PEG) delayed gastric emptying has been speculated as a cause of aspiration pneumonia.
- Trial name
- Elental (NCT01467765)
- Testing
- Elental
- Where
- Japan
- Volunteers
- 20 people
- Sponsor
- Showa Inan General Hospital
Soft Tissue Inflammation
Prevention of Hypergranulation Tissue After Gastrostomy Tube Placement
The primary objective of this study is to compare the incidence of postoperative hypergranulation tissue formation after gastrostomy tube placement among children randomized to one of three treatments, in addition to measuring…
- Trial name
- NCT01501539
- Testing
- Standard Hydrocolloid Dressing, Silver Hydrocolloid Dressing
- Where
- United States
- Volunteers
- 171 people
- Sponsor
- Ann & Robert H Lurie Children's Hospital of Chicago
Feeding Behavior, Feeding Disorder of Infancy or Early Childhood
iKanEat: A Randomized-controlled, Multi-center Trial of Megestrol for Chronic Oral Food Refusal in Children
This is a multi-center, randomized, placebo-controlled, double-blind clinical trial. The primary focus of the study is the evaluation of the effectiveness of treatment with megestrol as part of a 24 week behavioral feeding…
- Trial name
- iKanEat (NCT03815019)
- Testing
- Megestrol Acetate, iKanEat Behavioral Intervention
- Where
- 8 sites in United States
- Volunteers
- 70 people, healthy volunteers welcome
- Sponsor
- University of Kansas Medical Center
Deglutition Disorders in Infants, Chronic Tube Feeding in Hospitalized Infants
Parent Implemented Oral Nutrition, Eating, and Esophageal Reflexes Reintegration Protocol: RCT
Feeding dysfunction remains a major unmet challenge among neonatal ICU survivors, frequently leading to prolonged tube feeding or gastrostomy at discharge, increased healthcare utilization, substantial socioeconomic burden, and…
- Trial name
- PIONEER (NCT07035912)
- Testing
- PIONEER Protocol
- Volunteers
- 130 people
- Sponsor
- Nationwide Children's Hospital
Gastrostomy Complications, Gastrostomy Size
Does the Thickness of the Gastrostomy Affect the Incidence of Complications? A Prospective Randomized Single-Center Study in Children
The goal of this interventional study is to compare two different sizes of a gastrostomy tube in children and the incidence of complications three months postoperatively.
- Conditions
- Gastrostomy Complications, Gastrostomy Size, Food Intolerance, Granuloma
- Trial name
- NCT07300865
- Testing
- 12 Fr gastrostomy tube/button, 14 Fr gastrostomy tube/button
- Where
- Sweden
- Volunteers
- 200 people
- Sponsor
- Therese Hössjer
Enteral Nutritional Support
Evaluation of Tolerance and Safety of Early Enteral Nutrition in Children After Percutaneous Endoscopic Gastrostomy Placement
There aren't sufficient randomized prospective controlled trials in pediatric population comparing the safety and tolerance of early feeding after PEG placement (3-4 hours).
- Trial name
- NCT02777541
- Testing
- Resumption of feeding 3 hours after PEG placement, Resumption of feeding 8 hours after PEG placement
- Where
- Poland
- Volunteers
- 100 people
- Sponsor
- Children's Memorial Health Institute, Poland
Enteral Nutrition, Enteral Feeding
Bolus Versus Continuous Feeding Regimens Post Gastrostomy Tube Placement
The purpose of this study is to determine the best way to feed children after they have a gastrostomy tube placed. The study compares bolus feeding to continuous feeding.
- Conditions
- Enteral Nutrition, Enteral Feeding, Gastrostomy Tube
- Trial name
- NCT02006953
- Testing
- Bolus feeding schedule following gastrostomy tube placement, Continuous chimney feeds following gastrostomy tube placement
- Where
- 2 sites in United States
- Volunteers
- 97 people
- Sponsor
- University of Michigan
Gastrostomy
Ultrasound for Evaluation of Percutaneous G-tube Position
The goal of this clinical trial is to compare using ultrasound imaging to look at the position of the gastrostomy tube (GT) against fluoroscopic imaging in pediatric patients who had a recent GT tube replacement.
- Trial name
- NCT06361498
- Testing
- Ultrasound Imaging
- Where
- United States
- Volunteers
- 10 people
- Sponsor
- University of North Carolina, Chapel Hill
Gastrostomy
CO2 vs Air Insufflation in Children Undergoing PEG
Ap¬plications of CO2 insufflation for endoscopic procedures have been reported for the performance of routine colonoscopy, small bowel endoscopy, endoscopic retro¬grade cholangiopancreatography (ERCP) and endoscopic submucosal…
- Trial name
- NCT04714021
- Testing
- CO2, air
- Where
- 7 sites in Belgium, Croatia and 5 more
- Volunteers
- 120 people
- Sponsor
- University Medical Centre Ljubljana
Feeding Delays, Neonates and Term Infants
BabySTrong II taVNS Feeding Trial
The long-term goal of this project is to develop a therapy to assist pre-term and term infants with brain injury overcome difficulties in learning to feed so that infants may be discharged home with their families and avoid the…
- Trial name
- BabySTrong II (NCT07049952)
- Testing
- taVNS, NAC and taVNS, inactive taVNS
- Where
- United States
- Volunteers
- 88 people
- Sponsor
- Medical University of South Carolina