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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 is a NA study that has completed, run by Endeavor Health. The registered enrollment target is 285 participants.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02062775
The ClinicalTrials.gov registry entry for NCT02062775 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 285 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Endeavor Health, which has 94 total studies on file at ClinicalTrials.gov.
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 reports 0 study locations.
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.
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