Actively Recruiting
The Effects of Post-Operative Interventions on Surgical Site Occurrences in AWR
Led by Ohio State University · Updated on 2025-03-27
300
Participants Needed
1
Research Sites
345 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Randomized controlled trial to compare SSO's in abdominal wall reconstruction patients using Prevena, Prineo, and traditional incisional dressings.
CONDITIONS
Official Title
The Effects of Post-Operative Interventions on Surgical Site Occurrences in AWR
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age over 18 years
- Patients presenting for elective ventral hernia repair
- Patients considered good surgical candidates with no active life-threatening cardiac, pulmonary, renal, or hematologic disease
- Patients who will have a closed incision after surgery
You will not qualify if you...
- Known allergy to any material used in wound treatments (Prevena, Prineo, or traditional dressings)
- Active smokers within the past 4 weeks
- Patients with active life-threatening cardiac, pulmonary, renal, or hematologic disease
- Patients undergoing emergency ventral hernia repair due to bowel strangulation, necrosis, or trauma
- Patients with severe systemic sepsis
- Patients with open wounds after surgery
- Patients with obvious pus in the wound
- Patients undergoing panniculectomy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Department of Plastic Surgery
Columbus, Ohio, United States, 43212
Actively Recruiting
Research Team
J
Jeffrey Janis, MD
CONTACT
B
Benjamin Sarac, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
SINGLE_GROUP
Primary Purpose
PREVENTION
Number of Arms
3
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