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

Ohio State University · NCT04906408

Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Status re-checked against ClinicalTrials.gov within the last 12 hours.

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

Being studied: Prevena; Prineo; Traditional

Conditions: Abdomen Hernia

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

Age > 18
Patients presenting for elective ventral hernia repair
Patients deemed to be good surgical candidates, with no active life-threatening cardiac disease, pulmonary disease, renal disease, hematologic disease -Patients who will have a closed incision following the surgery

Exclusion Criteria

Known allergy to any material used in any wound treatment (Prevena- Acrylic adhesive or silver, Prineo- Dermabond glue, Standard- Bacitracin, Xeroform, surgical tape) -Active smokers (within the past 4 weeks) presenting for elective hernia repair
Patients with active life-threatening cardiac disease, pulmonary disease, renal disease, hematologic disease presenting for elective ventral hernia repair
Patients presenting for emergent ventral hernia repair (in the setting of bowel strangulation, necrosis, penetrating trauma) as it will be difficult to consent those patients for the study preoperatively
Patients with severe systemic sepsis
Patients with frank purulence in the wound -Patients with an open wound following surgery -Patients undergoing a panniculectomy

Department of Plastic Surgery
Columbus, OH 43212
Site contact: Jeffrey Janis, MD · 614-293-8566 · Jeffrey.Janis@osumc.edu