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NCT02062775 · ClinicalTrials.gov registry record · NA
Comparison of Self-Fixating vs Non-Fixating Hernia Mesh
A NA study, sponsored by Endeavor Health.
- Completed
- Registry status
- NA
- Development phase
- 285
- Enrollment target
NCT02062775: Completed NA study, sponsored by Endeavor Health.
NCT02062775 is a NA study that has completed, run by Endeavor Health. The registered enrollment target is 285 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (80% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02062775, a NA study, has completed, sponsored by Endeavor Health.
- COMPLETED
- Registry status
- NA
- Development phase
- 285 participants
- Enrollment target
Study Summary
The purpose of this study is to determine if self-fixating polyester mesh will have lower incidence of chronic postoperative pain and recurrence than non-fixating polyester mesh when used for laparoscopic inguinal hernia repair.
Interventions
- PROCEDURE Use of self-fixating mesh for inguinal hernia repair
- PROCEDURE Use of non-fixating mesh for inguinal hernia repair
- PROCEDURE Absorbable tacks may be used in hernias >2cm
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 285 participants |
| Start Date | 2013-08 |
| Est. Completion | 2017-10-10 |
| Phase | NA |
What the finished NCT02062775 record still lists
NCT02062775 is an interventional study that assigns participants to a tested intervention. The registered 285 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 (80% lower).
The record links to 0 conditions, and to 3 interventions - of which Use of self-fixating mesh for inguinal hernia repair is the first listed.
NCT02062775 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02062775 about?
NCT02062775 is a clinical study titled "Comparison of Self-Fixating vs Non-Fixating Hernia Mesh". The purpose of this study is to determine if self-fixating polyester mesh will have lower incidence of chronic postoperative pain and recurrence than non-fixating polyester mesh when used for laparoscopic inguinal hernia repair.
What is the current status of trial NCT02062775?
This trial is currently completed. It is a NA study. The enrollment target is 285 participants. The study started on 2013-08. Estimated completion is 2017-10-10.
What interventions are being tested in trial NCT02062775?
The interventions under investigation include: Use of self-fixating mesh for inguinal hernia repair (PROCEDURE), Use of non-fixating mesh for inguinal hernia repair (PROCEDURE), Absorbable tacks may be used in hernias >2cm (PROCEDURE).
Who is sponsoring clinical trial NCT02062775?
This trial is sponsored by Endeavor Health, which has 94 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02062775's enrollment target sits among peer trials
285 377th of 2000 higher than 1,624 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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