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Stoma Ileostomy clinical trials

View clinical trials related to Stoma Ileostomy.

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NCT ID: NCT03462667 Completed - Stoma Ileostomy Clinical Trials

Intensive Preoperative Ostomy Education for the Radical Cystectomy Patient

StomABC
Start date: February 26, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to learn if the stoma boot camp is a good and effective way to help people adapt to life with a stoma after surgery.

NCT ID: NCT03424447 Recruiting - Ileostomy - Stoma Clinical Trials

Stimulation of the Efferent Loop Before Loop Ileostomy Closure

Start date: November 20, 2014
Phase: Phase 2
Study type: Interventional

The purpose of the study is to determine the impact of the efferent loop stimulation of a loop ileostomy prior to closure on postoperative complications such as ileus and hospital stay

NCT ID: NCT03200444 Completed - Stoma Ileostomy Clinical Trials

Evaluation of the Peel Force of New Adhesives From the Skin

Start date: July 3, 2017
Phase: N/A
Study type: Interventional

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

NCT ID: NCT03044262 Completed - Stoma Ileostomy Clinical Trials

Evaluation of the Influence of New Adhesives of Output on Skin

Start date: January 9, 2017
Phase: N/A
Study type: Interventional

The study investigates the impact real output has on peristomal skin covered by a newly developed adhesive and a standard adhesive

NCT ID: NCT03016195 Terminated - Stoma Ileostomy Clinical Trials

Evaluation of the Normal Range of Urinary Sodium Levels in Healthy Newborn Babies

USALTI
Start date: October 2016
Phase: N/A
Study type: Observational

Oral sodium supplementation is currently administered in cases of poor weight gain in infants particularly in patients who have undergone gastrointestinal surgical procedures. The decision to start oral supplementation is based on urinary sodium levels although the level at which to start treatment is variable as the range in normal, healthy infants is unknown. This study aims to ascertain the normal range of sodium in urine specimens collected from healthy newborn babies. It is believed that by increasing the level of salt in the intestine, glucose can be more easily be absorbed and therefore weight gain improved. Babies with conditions where they are at risk of salt depletion (i.e. those with a stoma) are currently administered oral sodium supplementation if they are failing to gain weight and have an associated 'low' urinary sodium level. Low levels of urinary sodium are considered to represent a state of low body sodium levels, as the kidneys attempt to reabsorb most of the sodium in the urine before it is excreted. Current practice varies widely as to the level below which treatment should be instigated. Some centres advise below 20 mmol/L (Birmingham Children's Hospital and Nottingham Children's Hospital guidelines), others below 10 mmol/L (University Children's Hospital, Zurich). In Glasgow, babies with poor weight gain are given sodium supplementation if urinary sodium levels are below 40 mmol/L. There are no documented ranges for the levels of urinary sodium in healthy, newborn babies. By determining the reference range of urinary sodium levels in healthy, term babies who are gaining weight appropriately, the investigators hope to be able to have a better understanding about both the level below which supplementation should be considered and the target range that should be aimed for.

NCT ID: NCT02887144 Completed - Stoma Ileostomy Clinical Trials

Investigating the Safety and Performance of SenSura Test Product in Subjects With Ileostomy

CP257
Start date: January 2016
Phase: N/A
Study type: Interventional

The aim of the current Investigation is to evaluate the safety and performance of SenSura test product 1pc flat and convex light compared with commercial SenSura.

NCT ID: NCT02043782 Completed - Stoma Ileostomy Clinical Trials

Investigation of a New 1-piece Convex Ostomy Product

Start date: January 2014
Phase: N/A
Study type: Interventional

The aim of the investigation was to investigate the performance and safety of a new ostomy product

NCT ID: NCT01994902 Completed - Stoma Ileostomy Clinical Trials

Investigation of Newly Developed Ostomy Products in Subjects With Ileostomy

Start date: November 2013
Phase: N/A
Study type: Interventional

The aim of the investigation was to investigate the performance and safety of a new ostomy product.

NCT ID: NCT01957475 Completed - Stoma - Ileostomy Clinical Trials

Investigation of Two Newly Developed 2-piece Convex Baseplates in Subjects With Ileostomy

Start date: April 2013
Phase: N/A
Study type: Interventional

The aim of the current investigation is to develop new soft and more flexible 2-piece convex ostomy appliances

NCT ID: NCT01800916 Completed - Stoma Ileostomy Clinical Trials

Safety and Performance of New 1-piece Ostomy Product

Start date: February 2013
Phase: N/A
Study type: Interventional

The aim of the the current investigation is to develop new soft and more flexible 1-piece ostomy products.