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Mesh Type in Ventral Hernia Repair | Clinical Trials | Clareo Health

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COMPLETEDNANCT03091790

Mesh Type in Ventral Hernia Repair

Ventral hernias are common following abdominal surgery. Currently, there is no equipoise on when synthetic and biologic meshes should be used. Among open ventral hernia repairs, half are repaired usin...

Lead sponsor: The University of Texas Health Science Center, Houston•1 U.S. locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

The University of Texas Health Science Center, Houston

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•Patient scheduled for open ventral hernia repair at LBJ General Hospital

Exclusion Criteria

•Active infection
•Patient unlikely to survive with the next 2 years based upon surgeon judgment (i.e. metastatic cancer, end-stage cirrhosis)
•Patient surgeon would not normally place a prosthetic (e.g. planned second surgery such as ostomy takedown)
•Patient unlikely to follow-up (i.e. no phone)

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: June 22, 2023Terms

Trial snapshot

StatusCOMPLETED

PhaseNA

Enrollment87

Start dateMar 2017

Last updatedJun 22, 2023

Condition

Locations shown

UT Health at Lyndon B. Johnson General Hospital

Houston, Texas

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: June 22, 2023Data synced to Clareo: May 25, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions