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Ileostomy - Stoma clinical trials

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NCT ID: NCT03765606 Completed - Ileostomy - Stoma Clinical Trials

Cocoa Ileostomy Study

Start date: April 9, 2018
Phase: N/A
Study type: Interventional

There is substantial interest in the potential role of chocolate and its primary bioactive component; flavan-3-ol, (-)-epicatechin, in both the prevention and management of cardiovascular disease (CVD). Numerous observational studies have found the association between high cocoa intake and a reduced CVD risk and mortality, yet the impact of these mechanisms in vivo is unclear. In order to have a beneficial effect, these cocoa flavan-3-ols must be absorbed in the body in a forms, while still maintaining its advantageous characteristics. Consumption studies with ileostomists who have had their colon removed,provide information regarding the bioavailability and bioactivity of (-)-epicatechin and flavan-3-ols from cocoa, therefore the aim of this study is to determine the impact of methylaxanthines (including theobromine) on bioavailability of cocoa flavan-3-ols prior to entering the colon. This study has a randomised double blinded crossover control design, being applied to ileostomy patients who are aged 18-65 years, N=10, 5 per group. The study is divided into two phases. During the first phase, subjects will partake in a 2-day restriction diet (No phenolic foods) and an overnight fast prior to sampling. Ileal fluid (0hr) is obtained from participants. They will then be asked to consume the cocoa flavanol beverage dissolved in 310g 1% milk. After this urine and ieal fluid is collected every 4 hours at 3 more time points and blood every hour at 8 time points. A 24 hr urine and ieal fluid sample is collected the following day. There will be a 1-week wash out period between each phase. Procedure is repeated again for phase 2.

NCT ID: NCT03750461 Completed - Rectal Cancer Clinical Trials

Stoma Closure and Reinforcement Trial

SCAR
Start date: January 1, 2019
Phase: N/A
Study type: Interventional

Hernia formation at sites of ostomy closure is a common complication. The investigator believes that using evidence based hernia repair techniques as a preventive measure during closure of ostomies will reduce the incidence of hernia formation. In this trial, the investigator will pilot a novel technique of large pore monofilament polypropylene mesh reinforcement of the abdominal wall defects that remain after closure of an ileostomy to evaluate for safety and begin to evaluate the effectiveness compared to standard techniques.

NCT ID: NCT03439241 Completed - Ileostomy - Stoma Clinical Trials

Assessment of the Performance of a New Ostomy Device in Subjects Having an Ileostomy

Start date: February 5, 2018
Phase: N/A
Study type: Interventional

The purpose was to investigate the performance of a new ostomy device measured with a measuring device.

NCT ID: NCT03427203 Completed - Ileostomy - Stoma Clinical Trials

Assessment of New Ostomy Devices in Subjects Having an Ileostomy

Start date: January 9, 2018
Phase: N/A
Study type: Interventional

The study investigates the performance of three new adhesives with regard to leakage and the skin condition.

NCT ID: NCT03423134 Completed - Ileostomy - Stoma Clinical Trials

Investigating the Performance of a New Adhesive Strip

Start date: January 25, 2018
Phase: N/A
Study type: Interventional

This study investigates the performance of a new adhesive

NCT ID: NCT03419013 Completed - Ileostomy - Stoma Clinical Trials

Evaluation of the Performance of an Adhesive Strip

Start date: January 10, 2018
Phase: N/A
Study type: Interventional

This study investigated the performance of a new adhesive strip when impacted by output

NCT ID: NCT03348709 Completed - Clinical trials for Short Bowel Syndrome

Osmolality of Oral Supplements and Ileostomy Output

Start date: June 1, 2017
Phase: N/A
Study type: Interventional

This double-blinded, active comparator, cross-over intervention study tested the impact of two different oral supplements on ileostomy output volume and urinary sodium excretion and intestinal aquaporin expression in eight compensated patients with an ileostomy and not on home parenteral Nutrition or fluid support.

NCT ID: NCT03331783 Completed - Ileostomy - Stoma Clinical Trials

Assessment of the Effect of Output on New Adhesives

Start date: September 27, 2017
Phase: N/A
Study type: Interventional

The study investigates the impact real output has on adhesion of new adhesives

NCT ID: NCT03289013 Completed - Ileostomy - Stoma Clinical Trials

Assessement of the Peal Force Needed to Peel New Adhesives From the Skin

Start date: September 11, 2017
Phase: N/A
Study type: Interventional

This study investigates the adhesion of new adhesives to the skin.

NCT ID: NCT03257787 Completed - Ileostomy - Stoma Clinical Trials

Evaluation of the Performance of a New Adhesive Strip

Start date: August 8, 2017
Phase: N/A
Study type: Interventional

This study investigates the performance of a new adhesive strip when impacted by output.