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Feeding Tube Complication clinical trials

View clinical trials related to Feeding Tube Complication.

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NCT ID: NCT05694299 Recruiting - Feeding Disorders Clinical Trials

Nasal Bridle Versus Nasal Patch for Fixation of Nasoenteral Feeding Tubes

FIXIT
Start date: November 1, 2021
Phase: N/A
Study type: Interventional

Aim of this study is to compare fixation of nasoenteral feeding tubes using either a nasal patch or a nasal bridle in clinical patients with regard to the occurrence of tube dislocation, complications, and discomfort. 78 (2 * 39) eligible patients will be included in this randomized controlled trial. The study is executed in two general teaching hospitals in the Netherlands (Gelre Hospitals Apeldoorn and Medical Spectrum Twente).

NCT ID: NCT05653843 Recruiting - Endoscopy Clinical Trials

MANTIS Endoscopic Clipping Study

Start date: March 28, 2023
Phase:
Study type: Observational

This study is intended to document clinical effectiveness and safety pertaining to use of a new endoscopic clipping device MANTIS™ when used for hemostasis, closure, anchoring and marking.

NCT ID: NCT05557396 Withdrawn - Clinical trials for Feeding Tube Complication

Internal Tube Length of the Nasogastric Tube

Start date: September 1, 2022
Phase: N/A
Study type: Interventional

This methodological research is aimed to examine the effectiveness of the methods used to estimate the internal length of the nasogastric tube and to determine the most reliable method for correct placement of the nasogastric tube in adults. The study will be carried out between 01 September 2022 and 01 September 2023 with 155 patients who hospitalized in the anesthesia and reamination intensive care and general intensive care units of Aydın Adnan Menderes University Application and Research Hospital. The internal tube length measurement methodologies will utilized to confirm proper NGT placement. A total of 5 groups will be included in the study, including 1 control (NEX measurement method) and 4 experimental groups, (Experiment 1: CoNEX measurement method, Experiment 2: XEN+10 cm measurement method, Experiment 3: GWNUF measurement method, Experiment 4: EXU-NE Method measurement method).The "gold standard" reference method will used for comparison was radiography. Research data will be analyzed in SPSS (Statistical Package for Social Sciences) for Windows 25.0 statistical package program. Descriptive statistical methods (number, percentage, mean, standard deviation) will be used in the evaluation of the data. The comparison between the methods used in the measurement of the nasogastric tube (NEX, CoNEX, XEN+10 cm, GWNUF, EXU-NE) and the results of the radiological evaluation (reference method) will be made with Chi-square analysis. Statistical significance will be accepted as p<0.05.

NCT ID: NCT05288556 Active, not recruiting - Clinical trials for Feeding Tube Complication

Safety and Efficacy of Enteral Feeding Tube Stoma Site Accessory

SSA
Start date: April 22, 2022
Phase: N/A
Study type: Interventional

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. This accessory has been developed by the Cleveland Clinic and will be used for the first time in human subjects according to the labeled indication for clinical use in accordance with the Manufacturer's Instructions for Use based on other similar, FDA approved gastrostomy and jejunostomy enteral feeding tube accessory components. After providing informed consent, eligible patients will receive a study stoma site accessory during a feeding tube replacement procedure the patient is scheduled to have as a standard of care procedure.

NCT ID: NCT04627844 Not yet recruiting - Clinical trials for Feeding Tube Complication

Time to Feeding After PEG Tube Placement.

Start date: November 2020
Phase: Phase 4
Study type: Interventional

Trauma patients who require Percutaneous Endoscopic Gastrostomy (PEG) tube placement for feeding and who consent to be in the study will be randomized to receive feeding at either 6 hours after PEG placement as is routinely done or at 0 hours after PEG placement.

NCT ID: NCT04621734 Completed - Clinical trials for Feeding Tube Complication

Retention of Nasoenteric Feeding Tubes in Pediatric Patients Using a Nasal Bridle

Start date: February 18, 2020
Phase: N/A
Study type: Interventional

A study to compare tube dislodgment rates when a nasoenteric feeding tube is secured with adhesive tape vs the AMT BridlePro device.