Clinical trials: Feeding Tube
Hemostasis, Perforation Colon
MANTIS Endoscopic Clipping Study
This study is intended to document procedural and clinical effectiveness in consecutive cases in which at least one MANTIS clip is selected, pertaining to use of a new endoscopic clipping device MANTIS™ including but not limited…
- Conditions
- Hemostasis, Perforation Colon, Feeding Tube Complication, Endoscopy
- Trial name
- NCT05653843
- Testing
- Endoscopic clip placement in the gastrointestinal tract.
- Where
- 10 sites in United States, Canada and 4 more
- Volunteers
- 240 people
- Sponsor
- Boston Scientific Corporation
Feeding Tube
Self-Propelled Versus Standard Percutaneous Endoscopic Gastrojejunostomy(PEG-J); RCT
Our main hypothesis is that self-propelled Percutaneous Endoscopic Gastrojejunostomy tube (PEG-J) that has a balloon on it's tip is associated with lower J-tube retrograde migration rate, and lower rates of short- and long-term…
- Trial name
- NCT01892267
- Testing
- PEG-J placement
- Where
- United States
- Volunteers
- 19 people
- Sponsor
- Johns Hopkins University
Body Temperature
Temperature Monitoring With InnerSense Esophageal Temperature Sensor/Feeding Tube After Birth Through Stabilization in VLBW Infants
Very low birth weight (VLBW) infants (<1500 grams at birth) and other low birth weight infants experience hypothermia after birth and through stabilization (first 24 hours of life) due to an inability to keep warm through…
- Trial name
- NCT02311972
- Testing
- Philips InnerSense Esophageal Temperature Sensor/Feeding Tube, Standard of care feeding tube
- Where
- United States
- Volunteers
- 52 people
- Sponsor
- Duke University
Enteral Feeding Intolerance
Optimal Feeding Tube Placement
A randomized controlled trial comparing current standard blind method to CORTRAK enteral access system (CEAS), an FDA approved electromagnetic device to place enteric tubes.
- Trial name
- NCT04241146
- Testing
- Enteric Tube, CORTRAK enteral access system
- Where
- United States
- Volunteers
- 52 people
- Sponsor
- The University of Texas Health Science Center at San Antonio
Preterm Birth, Tube Feeding
Maternal Role in Oral Feed Establishment in Preterm Neonates
Hypothesis Preterm babies who receive sensory motor stimulation from their mothers as compared to trained nurses will 1. Start taking oral feed at the same time as compared to control group 2.
- Conditions
- Preterm Birth, Tube Feeding, Swallowing Disorder, Maternal Care Patterns
- Trial name
- NCT05484726
- Testing
- perioral sensory motor stimulation
- Where
- Pakistan
- Volunteers
- 130 people, healthy volunteers welcome
- Sponsor
- Fatima Memorial Hospital
Infection
Optimal Feeding Tube Dwell Time in VLBW Infants to Reduce Feeding Tube Contamination
The study team will determine whether a decreased feeding tube dwell time will reduce feeding tube contamination
- Trial name
- NCT03728608
- Testing
- Feeding tube dwell time of 48 hours, Feeding tube dwell time of 7 day
- Where
- United States
- Volunteers
- 151 people
- Sponsor
- University of Florida
Enteral Nutrition
TubeClear® Evaluation in Pediatric Patients (Phase I)
This is the first of three planned phases designed to evaluate the feasibility and tolerability of TubeClear® to restore patency in occluded Pediatric Enteral Access Devices.
- Trial name
- NCT02724631
- Testing
- TubeClear® intervention
- Where
- United States
- Volunteers
- 1 people
- Sponsor
- Children's Hospital of Philadelphia
GERD
Self-Propelled Percutaneous Endoscopic GastroJejunostomy (PEG-J)
This research is being done to study the safety of an investigational percutaneous endoscopic gastrojejunostomy (PEGJ) tube and whether the addition of a balloon on the end of the J tube prevents it from slipping back into the…
- Trial name
- NCT01551095
- Testing
- PEGJ tube
- Where
- United States
- Volunteers
- 7 people
- Sponsor
- Johns Hopkins University
Critical Illness
The Energy Dose Study
The investigators have designed this single-center Randomized Clinical Trial (RCT) to prospectively compare, for the first time, the clinical efficacy of different energy doses in intensive care unit (ICU) patients requiring…
- Trial name
- NCT01369147
- Testing
- Parenteral Nutrition, Propofol, Clevidipine
- Where
- United States
- Volunteers
- 12 people
- Sponsor
- Emory University
Enteral Nutrition
DrIFT 2 Study: Displacement in Feeding Tubes
The proposed study will use an electromagnetic placement device (EMPD), Cortrak* 2 Enteral Access System (EAS™), Avanos Medical, to verify feeding tube (FT) position on a daily basis to assess for migration.
- Trial name
- NCT06239610
- Testing
- electromagnetic placement device
- Where
- United States
- Volunteers
- 119 people
- Sponsor
- Parkview Health
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
Type 2 Diabetes
Evaluation of White Sweet Potato Tube Feeding Formula on Type 2 Diabetic Residents in Long-term Care Institutions
In order to response the increasing of aging population cause losing ability that need long-care needs, the project entitled "10-year long-term care program" from Executive Yuan in 2007 is carried out to assist economically…
- Trial name
- NCT02711839
- Testing
- Commercial diabetic formula, White sweet potato formula
- Volunteers
- 54 people
- Sponsor
- Taipei Medical University
Feeding Tube Complication
Safety and Efficacy of Enteral Feeding Tube Stoma Site Accessory
The purpose of the study is to collect safety and efficacy data on the performance of the study stoma site accessory when used to prevent abdominal wall leakage for patients with a long term feeding tube.
- Trial name
- SSA (NCT05288556)
- Testing
- Placement of stoma site enteral feeding tube accessory
- Where
- United States
- Volunteers
- 5 people
- Sponsor
- Eric Yudelevich
Enteral Feeding in Bronchiolitis
Comparison Between Gastric and Post Pyloric Tube Feedings in Children With Bronchiolitis Requiring High Flow Nasal Cannula
The purpose of the study is to compare two ways (nasogastric tube (NGT) and nasoduodenal tube (NDT)) to provide nutrition to infants admitted to the hospital for viral bronchiolitis and who require high flow nasal cannula therapy.
- Trial name
- NCT03346850
- Testing
- Nasogastric tube (NGT) feeding, Nasoduodenal tube (NDT) feeding
- Where
- United States
- Volunteers
- 40 people
- Sponsor
- The University of Texas Health Science Center, Houston
Feeding Tube Complication
Retention of Nasoenteric Feeding Tubes in Pediatric Patients Using a Nasal Bridle
A study to compare tube dislodgment rates when a nasoenteric feeding tube is secured with adhesive tape vs the AMT BridlePro device.
- Trial name
- NCT04621734
- Testing
- AMT BridlePro Device, Adhesive Tape
- Where
- United States
- Volunteers
- 35 people
- Sponsor
- The University of Texas Health Science Center at San Antonio
Enteral Nutrition
Feasibility Study to Evaluate Safety of ENvizion Medical™ ENVUE™ System
This is a single center, non-randomized feasibility clinical evaluation that is designed to affirm the safety of the ENVUE™ System guidance during the placement of the ENvizion Medical™ enteral feeding tubes.
- Trial name
- NCT03505593
- Testing
- ENVUE System
- Where
- United States
- Volunteers
- 48 people
- Sponsor
- Envizion Medical Ltd.
Oropharyngeal Dysphagia (OPD), Dysphagia
Safety and Efficacy of the Swallow Expansion Device (SED) for Improvement of Swallowing in Patients
Biomedical devices, such as artificial joints and pacemakers, are accepted and commonly used in medicine. While great progress in biomedical devices has been made for many other disorders, there is currently no device available…
- Trial name
- NCT02296528
- Testing
- Swallowing Expansion Device
- Where
- United States
- Volunteers
- 4 people
- Sponsor
- Peter Belafsky, MD
Amyotrophic Lateral Sclerosis
High Fat/High Calorie Trial in Amyotrophic Lateral Sclerosis
The purpose of this study is to determine the safety, tolerability, and preliminary efficacy of long-term use of high fat/high calorie and high calorie diets in people with amyotrophic lateral sclerosis (ALS) (Lou Gehrig's…
- Trial name
- NCT00983983
- Testing
- Oxepa, Jevity 1.5, Jevity 1.0
- Where
- 13 sites in United States
- Volunteers
- 28 people
- Sponsor
- Massachusetts General Hospital
Enteral Nutrition
Feasibility Study to Evaluate Safety of Nutriseal™ Nutriplace™ System
This is a single center, non-randomized feasibility clinical evaluation that is designed to affirm the safety of the Nutriplace™ System guidance during the placement of the Nutriseal™ enteral feeding tubes.
- Trial name
- NCT03371160
- Testing
- Nutriplace™ System
- Where
- United States
- Volunteers
- 22 people
- Sponsor
- Nutriseal L.P
Feeding Disorders
Nasal Bridles and Repeat Endoscopic Procedures for Endoscopic Nasoenteric Tubes
In critically ill patients, nutrition is a major part of healing and recovery. In patients unable to tolerate oral feeding, nasoenteric tube feeding (a tube placed from the nose to the stomach or small intestine) provides a safe…
- Trial name
- NCT03966157
- Testing
- Nasal Bridle
- Where
- United States
- Volunteers
- 31 people, healthy volunteers welcome
- Sponsor
- St. Louis University