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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 is a Phase 4 study that has completed, run by Cytori Therapeutics. The registered enrollment target is 60 participants.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00531739
The ClinicalTrials.gov registry entry for NCT00531739 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cytori Therapeutics, which has 6 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Polylactic Acid Sheet is the first listed.
NCT00531739 reports 0 study locations.
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.
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