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NCT02712398 · ClinicalTrials.gov registry record · NA
A Prospective Trial of a Bio-absorbable Mesh in Challenging Laparoscopic Ventral or Incisional Hernia Repair
A NA study, sponsored by C. R. Bard.
- Completed
- Registry status
- NA
- Development phase
- 120
- Enrollment target
NCT02712398: Completed NA study, sponsored by C. R. Bard.
NCT02712398 is a NA study that has completed, run by C. R. Bard. The registered enrollment target is 120 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02712398, a NA study, has completed, sponsored by C. R. Bard.
- COMPLETED
- Registry status
- NA
- Development phase
- 120 participants
- Enrollment target
Study Summary
The objective of this study is to collect additional data on safety, performance and effectiveness of Phasix™ ST in subjects receiving laparoscopic ventral or incisional hernia repair at high risk for surgical site occurrence (SSO).
Primary Outcome
Proportion of subjects with Surgical Site Occurrences(SSO), which are defined as hematoma, seroma, surgical site infection, wound dehiscence, skin necrosis and fistula requiring intervention. Occurrences at the surgical site will be assessed by physical examination at each study visit through 45 days.
Interventions
- DEVICE Phasix™ ST
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 120 participants |
| Start Date | 2016-04 |
| Est. Completion | 2019-11-15 |
| Phase | NA |
What the finished NCT02712398 record still lists
NCT02712398 is an interventional study that assigns participants to a tested intervention. The registered 120 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower).
The record links to 0 conditions, and to 1 intervention - of which Phasix™ ST is the first listed.
NCT02712398 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02712398 about?
NCT02712398 is a clinical study titled "A Prospective Trial of a Bio-absorbable Mesh in Challenging Laparoscopic Ventral or Incisional Hernia Repair". The objective of this study is to collect additional data on safety, performance and effectiveness of Phasix™ ST in subjects receiving laparoscopic ventral or incisional hernia repair at high risk for surgical site occurrence (SSO).
What is the current status of trial NCT02712398?
This trial is currently completed. It is a NA study. The enrollment target is 120 participants. The study started on 2016-04. Estimated completion is 2019-11-15.
What interventions are being tested in trial NCT02712398?
The interventions under investigation include: Phasix™ ST (DEVICE).
Who is sponsoring clinical trial NCT02712398?
This trial is sponsored by C. R. Bard, which has 75 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02712398's enrollment target sits among peer trials
120 762nd of 2000 higher than 1,198 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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