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NCT00531739 · ClinicalTrials.gov registry record · Phase 4
SurgiWrapTM to Reduce Soft Tissue Attachment & Incidence Early Post-Operative Bowel Obstruction in Colorectal Surgery
A Phase 4 study, sponsored by Cytori Therapeutics.
- Completed
- Registry status
- Phase 4
- Development phase
- 60
- Enrollment target
NCT00531739: Completed Phase 4 study, sponsored by Cytori Therapeutics.
NCT00531739 is a Phase 4 study that has completed, run by Cytori Therapeutics. The registered enrollment target is 60 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (88% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00531739, a Phase 4 study, has completed, sponsored by Cytori Therapeutics.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 60 participants
- Enrollment target
Study Summary
The purpose of this study is to determine if the use of SurgiWrapTM: (1) prevents/lowers the incidence of Grade 2 or higher soft tissue attachments under the incision made during abdominal surgery, (2) reduces post-operative bowel obstruction.
Interventions
- OTHER Polylactic Acid Sheet
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2006-03 |
| Est. Completion | 2009-07 |
| Phase | Phase 4 |
What the finished NCT00531739 record still lists
NCT00531739 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (88% lower).
The record links to 0 conditions, and to 1 intervention - of which Polylactic Acid Sheet is the first listed.
NCT00531739 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00531739 about?
NCT00531739 is a clinical study titled "SurgiWrapTM to Reduce Soft Tissue Attachment & Incidence Early Post-Operative Bowel Obstruction in Colorectal Surgery". The purpose of this study is to determine if the use of SurgiWrapTM: (1) prevents/lowers the incidence of Grade 2 or higher soft tissue attachments under the incision made during abdominal surgery, (2) reduces post-operative bowel obstruction.
What is the current status of trial NCT00531739?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 60 participants. The study started on 2006-03. Estimated completion is 2009-07.
What interventions are being tested in trial NCT00531739?
The interventions under investigation include: Polylactic Acid Sheet (OTHER).
Who is sponsoring clinical trial NCT00531739?
This trial is sponsored by Cytori Therapeutics, which has 6 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00531739's enrollment target sits among peer trials
60 1125th of 2000 higher than 799 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 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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