Biologic Mesh Versus Synthetic Mesh in Repair of Ventral Hernias
Summary
The registered summary isn't in our current data snapshot. Read it on the ClinicalTrials.gov record ↗. Why? →
Investigators
The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.
- Michael Rosen, MD
Cleveland Clinic, Cleveland, Ohio, United States, 44195
Principal Investigator
A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.
Sites
4 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.
- Washington University in St. Louis School of Medicine
St Louis, Missouri, United States
- Cleveland Clinic
Cleveland, Ohio, United States
- University of South Carolina School of Medicine
Greenville, South Carolina, United States
- Vanderbilt University
Nashville, Tennessee, United States
Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.
Drugs studied
No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →
Registration & key dates
Registry attributes as recorded on the ClinicalTrials.gov study record.
- Start
- 30 Apr 2015
- Primary completion
- 1 Apr 2021
- Completion
- 1 Apr 2021
- Last update posted
- 7 Sept 2022
- Registered enrollment
- 253
- Registry id
- NCT02451176
Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 12 Jul 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.