MedTrace Logo

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

NCT04906408 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 300

Last updated 2025-03-27

No results posted yet for this study

Summary

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

Conditions

  • Abdomen Hernia

Interventions

DEVICE

Prevena

Incisions will be dressed with closed incisional negative pressure wound therapy

DEVICE

Prineo

Incisions will be dressed with Prineo

DRUG

Traditional

Incisions will be dressed with bacitracin/xeroform

Sponsors & Collaborators

  • Ohio State University

    lead OTHER

Principal Investigators

  • Jeffrey E Janis, MD · Ohio State University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-09-17
Primary Completion
2028-05-01
Completion
2028-05-01
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

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 NCT04906408 on ClinicalTrials.gov