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NCT01589822 · ClinicalTrials.gov registry record · Phase 2
The EVICEL® Gastrointestinal Study
A Phase 2 study, sponsored by Ethicon.
- Completed
- Registry status
- Phase 2
- Development phase
- 214
- Enrollment target
NCT01589822: Completed Phase 2 study, sponsored by Ethicon.
NCT01589822 is a Phase 2 study that has completed, run by Ethicon. The registered enrollment target is 214 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (61% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01589822, a Phase 2 study, has completed, sponsored by Ethicon.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 214 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the safety and effectiveness of EVICEL® Fibrin Sealant (Human) for use as an adjunct to gastrointestinal (GI) surgery.
Interventions
- BIOLOGICAL EVICEL Fibrin Sealant
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 214 participants |
| Start Date | 2012-06 |
| Est. Completion | 2014-09 |
| Phase | Phase 2 |
What the finished NCT01589822 record still lists
NCT01589822 is an interventional study that assigns participants to a tested intervention. The registered 214 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (61% higher).
The record links to 0 conditions, and to 1 intervention - of which EVICEL Fibrin Sealant is the first listed.
NCT01589822 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01589822 about?
NCT01589822 is a clinical study titled "The EVICEL® Gastrointestinal Study". The purpose of this study is to evaluate the safety and effectiveness of EVICEL® Fibrin Sealant (Human) for use as an adjunct to gastrointestinal (GI) surgery.
What is the current status of trial NCT01589822?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 214 participants. The study started on 2012-06. Estimated completion is 2014-09.
What interventions are being tested in trial NCT01589822?
The interventions under investigation include: EVICEL Fibrin Sealant (BIOLOGICAL).
Who is sponsoring clinical trial NCT01589822?
This trial is sponsored by Ethicon, which has 38 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01589822's enrollment target sits among peer trials
214 290th of 2000 higher than 1,711 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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