Feasibility Study of a New Fistula Pouching System

Completed · Phase 2/Phase 3

Conditions studied: Cutaneous Fistula

In brief

The purpose of this investigation is to carry out a clinical evaluation of a newly developed fistula pouching system's ability to function as a good pouch for fistulas, with the opening on the skin of the stomach or in a wound on the skin of the stomach.

Key facts

Study ID

NCT00294450

Run by

Coloplast A/S

People needed

22

Starts

2006-02-01

Expected to finish

2007-03-01

Last updated by the study team

2012-02-01

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 18 years or older
• Capable of giving informed consent
• Have to be hospitalized
• Have a fistula with the opening on the skin in the abdominal area

You may not qualify if…

• Pregnant and/or breast-feeding
• Receiving radiation- or chemotherapy during the investigation period

Where it is running

• St. Francis Hospital and Medical Center — Hartford, Connecticut, United States
• Morton Plant Hospital — Clearwarter, Florida, United States
• Fairview Southdale Hospital — Edina, Minnesota, United States
• University of Minnesota Medical Center Fairview - Riverside — Minneapolis, Minnesota, United States
• University of Minnesota Medical Center Fairview — Minneapolis, Minnesota, United States
• The Cleveland Clinic Foundation — Cleveland, Ohio, United States
• Presbyterian Hospital of Dallas — Dallas, Texas, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.