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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 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.

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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.

Conditions Studied

Incisional Hernia

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

FieldValue
Enrollment Target 154 participants
Start Date 2022-11-14
Est. Completion 2031-10
Phase NA

Sponsor

Clayton Petro

5 total trials

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What the Registry Record Tells You About NCT05599750

The ClinicalTrials.gov registry entry for NCT05599750 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 154 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 293-participant average among 5 other Incisional Hernia trials with a reported enrollment target (47% lower). The listed sponsor is Clayton Petro, which has 5 total studies on file at ClinicalTrials.gov.

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 reports 5 study locations spanning 4 distinct geographic areas - top geographies include 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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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.