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COMPLETED Phase 2

Feasibility Study of a New Fistula Pouching System

NCT00294450 · View on ClinicalTrials.gov ↗

Study Summary

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.

Conditions Studied

Interventions

  • DEVICE Fistula Pouching System

Study Locations (7)

Minnesota

  • Fairview Southdale Hospital — Edina
  • University of Minnesota Medical Center Fairview - Riverside — Minneapolis
  • University of Minnesota Medical Center Fairview — Minneapolis

Connecticut

  • St. Francis Hospital and Medical Center — Hartford

Florida

  • Morton Plant Hospital — Clearwarter

Ohio

  • The Cleveland Clinic Foundation — Cleveland

Texas

  • Presbyterian Hospital of Dallas — Dallas

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2006-02
Est. Completion 2007-03
Phase Phase 2

Sponsor

Coloplast A/S

7 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00294450

The ClinicalTrials.gov registry entry for NCT00294450 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 22 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Coloplast A/S, which has 7 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Cutaneous Fistula appearing as the primary indexed condition, and to 1 intervention — of which Fistula Pouching System is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00294450 reports 7 study locations spanning 5 distinct geographic areas — top geographies include Minnesota, Connecticut, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00294450 about?

NCT00294450 is a clinical study titled "Feasibility Study of a New Fistula Pouching System". 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.

What is the current status of trial NCT00294450?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 22 participants. The study started on 2006-02. Estimated completion is 2007-03.

What conditions does trial NCT00294450 study?

This clinical trial studies the following conditions: Cutaneous Fistula. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00294450?

The interventions under investigation include: Fistula Pouching System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00294450?

This trial is sponsored by Coloplast A/S, which has 7 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00294450 being conducted?

This trial has 7 study locations across Connecticut, Florida, Minnesota, Ohio, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial