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NCT00559013 · ClinicalTrials.gov registry record · NA
Peri-Strips Dry (PSD) Veritas Collagen Matrix Staple Line Reinforcement for Colorectal Surgery
A NA study, sponsored by Baxter Healthcare Corporation.
- Completed
- Registry status
- NA
- Development phase
- 38
- Enrollment target
NCT00559013: Completed NA study, sponsored by Baxter Healthcare Corporation.
NCT00559013 is a NA study that has completed, run by Baxter Healthcare Corporation. The registered enrollment target is 38 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00559013, a NA study, has completed, sponsored by Baxter Healthcare Corporation.
- COMPLETED
- Registry status
- NA
- Development phase
- 38 participants
- Enrollment target
Study Summary
Purpose of the study is to assess the utility of PSD Veritas as a staple line reinforcement to minimize the risk of leakage during or after colo-rectal surgery.
Interventions
- DEVICE Staple line reinforcement
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 38 participants |
| Start Date | 2007-03 |
| Est. Completion | 2008-12 |
| Phase | NA |
What the finished NCT00559013 record still lists
NCT00559013 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 38 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).
The record links to 0 conditions, and to 1 intervention - of which Staple line reinforcement is the first listed.
NCT00559013 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00559013 about?
NCT00559013 is a clinical study titled "Peri-Strips Dry (PSD) Veritas Collagen Matrix Staple Line Reinforcement for Colorectal Surgery". Purpose of the study is to assess the utility of PSD Veritas as a staple line reinforcement to minimize the risk of leakage during or after colo-rectal surgery.
What is the current status of trial NCT00559013?
This trial is currently completed. It is a NA study. The enrollment target is 38 participants. The study started on 2007-03. Estimated completion is 2008-12.
What interventions are being tested in trial NCT00559013?
The interventions under investigation include: Staple line reinforcement (DEVICE).
Who is sponsoring clinical trial NCT00559013?
This trial is sponsored by Baxter Healthcare Corporation, which has 46 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00559013's enrollment target sits among peer trials
38 1538th of 2000 higher than 461 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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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