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Heavy Weight Versus Medium Weight Mesh in Ventral Hernia Repair

NCT03082391 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 350

Last updated 2022-07-14

Study results available
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Summary

The purpose of this study is to determine if mesh weight has an impact on postoperative pain, ventral hernia recurrence, incidence of deep wound infection, and overall quality of life following ventral hernia repair with mesh.

Conditions

  • Ventral Hernia

Interventions

DEVICE

Heavy weight Mesh

Patients will undergo ventral hernia repair with heavy weight mesh.

DEVICE

Medium weight Mesh

Patients will undergo ventral hernia repair with medium weight mesh.

Sponsors & Collaborators

  • The Cleveland Clinic

    lead OTHER

Principal Investigators

  • Michael J Rosen, MD · The Cleveland Clinic

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-03-14
Primary Completion
2020-05-28
Completion
2020-05-28
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03082391 on ClinicalTrials.gov