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Study identifier: NCT04906408 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

The Effects of Post-Operative Interventions on Surgical Site Occurrences in AWR

Condition: Abdomen Hernia  ·  Sponsor: Ohio State University

PhaseNA
Planned participants300
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

Randomized controlled trial to compare SSO's in abdominal wall reconstruction patients using Prevena, Prineo, and traditional incisional dressings.

This description comes directly from the study's public registry record.

Talk to the study team

Jeffrey Janis, MD  ·  6143661242  ·  Jeffrey.Janis@osumc.edu

Benjamin Sarac, MD  ·  6143661242  ·  Benjamin.Sarac@osumc.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Department of Plastic SurgeryColumbus, Ohio, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT04906408