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RECRUITING NA

Suture Repair vs Mesh Repair for Incisional Hernia

NCT05599750 · View on ClinicalTrials.gov ↗

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

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

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05599750

The ClinicalTrials.gov registry entry for NCT05599750 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 154 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Clayton Petro, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05599750 reports 5 study locations spanning 4 distinct geographic areas — top geographies include Ohio, Florida, Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05599750?

The interventions under investigation include: Incisional hernia repair (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05599750?

This trial is sponsored by Clayton Petro, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial