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NCT05599750 · ClinicalTrials.gov registry record · NA
Suture Repair vs Mesh Repair for Incisional Hernia
A NA study of Incisional Hernia, sponsored by Clayton Petro.
- Recruiting
- Registry status
- NA
- Development phase
- 154
- Enrollment target
- 5
- Study locations
NCT05599750: Recruiting NA study of Incisional Hernia, sponsored by Clayton Petro.
NCT05599750 is a NA study of Incisional Hernia that is actively recruiting participants, run by Clayton Petro. The registered enrollment target is 154 participants, below the 293-participant average among 5 other Incisional Hernia trials with a reported enrollment target (47% lower). The trial reports 5 study locations across 4 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05599750, a NA study of Incisional Hernia, is actively recruiting participants, sponsored by Clayton Petro.
- RECRUITING
- Registry status
- NA
- Development phase
- 154 participants
- Enrollment target
- 5
- Study locations
Study Summary
The goal of this randomized controlled trial is to compare the difference in quality of life at one year postoperatively for patients undergoing incisional hernia repair with mesh versus suture repair using modern techniques. The main question it aims to answer are: • Determine if primary suture repair is non-inferior to mesh repair for incisional hernias 2-6cm with respect to quality of life using the HerQLes summary score at one year postoperatively.
Primary Outcome
Suture repair will be compared to mesh repair for incisional hernias 2-6cm with respect to quality of life using the Hernia-specific Quality of Life (HerQLes) summary score at one year postoperatively. This is reported as a score from 0-100 with higher numbers indicating better quality of life.
Conditions Studied
Interventions
- PROCEDURE Incisional hernia repair
Study Locations (5)
Ohio
- Cleveland Clinic Main Campus - Cleveland
- The Ohio State University Wexner Medical Center - Columbus
Florida
- University of Florida - Gainesville
Illinois
- Northwestern - Chicago
Tennessee
- Vanderbilt University - Nashville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 154 participants |
| Start Date | 2022-11-14 |
| Est. Completion | 2031-10 |
| Phase | NA |
What NCT05599750 shows while recruiting
NCT05599750 is an interventional study that assigns participants to a tested intervention. The registered 154 participants enrollment target is mid-sized for trials with a published cap, below the 293-participant average among 5 other Incisional Hernia trials with a reported enrollment target (47% lower).
The record links to 1 condition, with Incisional Hernia appearing as the primary indexed condition, and to 1 intervention - of which Incisional hernia repair is the first listed.
NCT05599750 lists 5 locations in 4 states (Ohio, Florida, Illinois).
Frequently Asked Questions
What is clinical trial NCT05599750 about?
NCT05599750 is a clinical study titled "Suture Repair vs Mesh Repair for Incisional Hernia". The goal of this randomized controlled trial is to compare the difference in quality of life at one year postoperatively for patients undergoing incisional hernia repair with mesh versus suture repair using modern techniques. The main question it aims to answer are: • Determine if primary suture r...
What is the current status of trial NCT05599750?
This trial is currently recruiting. It is a NA study. The enrollment target is 154 participants. The study started on 2022-11-14. Estimated completion is 2031-10.
What conditions does trial NCT05599750 study?
This clinical trial studies the following conditions: Incisional Hernia.
What interventions are being tested in trial NCT05599750?
The interventions under investigation include: Incisional hernia repair (PROCEDURE).
Who is sponsoring clinical trial NCT05599750?
This trial is sponsored by Clayton Petro, which has 5 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05599750 being conducted?
This trial has 5 study locations across Florida, Illinois, Ohio, Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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