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NCT00820040 · ClinicalTrials.gov registry record · Phase 2
Feasibility of Permacol Use in Infected Fields
A Phase 2 study, sponsored by Medtronic - MITG.
- Terminated
- Registry status
- Phase 2
- Development phase
- 10
- Enrollment target
NCT00820040: Clinical Trial Phase 2 study, sponsored by Medtronic - MITG.
NCT00820040 is a Phase 2 study that was terminated before completion, run by Medtronic - MITG. The registered enrollment target is 10 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00820040, a Phase 2 study, was terminated before completion, sponsored by Medtronic - MITG.
- TERMINATED
- Registry status
- Phase 2
- Development phase
- 10 participants
- Enrollment target
Study Summary
This pilot study is to examine the feasibility of using Permacol Surgical Implant in the repair of abdominal wall defects after removal of infected prosthetic mesh
Primary Outcome
The primary objective of this study was hernia recurrence or surgical site infection as assessed by a CT scan 12 months following surgery.Hernia recurrence was defined as any abnormal abdominal protrusion, as assessed by 12 month CT. Surgical site infection requiring wound opening was defined as abscess formation or drainage that required surgical wound opening. Wound opening was defined as surgical entry into the wound.
Interventions
- DEVICE acellular porcine dermal collagen mesh
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10 participants |
| Start Date | 2009-07 |
| Est. Completion | 2011-08 |
| Phase | Phase 2 |
Why NCT00820040 stopped before completion
NCT00820040 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower).
The record links to 0 conditions, and to 1 intervention - of which acellular porcine dermal collagen mesh is the first listed.
NCT00820040 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00820040 about?
NCT00820040 is a clinical study titled "Feasibility of Permacol Use in Infected Fields". This pilot study is to examine the feasibility of using Permacol Surgical Implant in the repair of abdominal wall defects after removal of infected prosthetic mesh
What is the current status of trial NCT00820040?
This trial is currently terminated. It is a Phase 2 study. The enrollment target is 10 participants. The study started on 2009-07. Estimated completion is 2011-08.
What interventions are being tested in trial NCT00820040?
The interventions under investigation include: acellular porcine dermal collagen mesh (DEVICE).
Who is sponsoring clinical trial NCT00820040?
This trial is sponsored by Medtronic - MITG, which has 119 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00820040's enrollment target sits among peer trials
10 1968th of 2000 higher than 12 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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