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

Description

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

Conditions

Abdomen Hernia

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Study Overview

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Study Details

Study overview

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

The Effects of Post-Operative Interventions on Surgical Site Occurrences in Abdominal Wall Reconstructions: A Randomized Controlled Trial

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

Condition
Abdomen Hernia
Intervention / Treatment

-

Contacts and Locations

Columbus

Department of Plastic Surgery, Columbus, Ohio, United States, 43212

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility 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
  • * 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

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Ohio State University,

Jeffrey E Janis, MD, PRINCIPAL_INVESTIGATOR, Ohio State University

Study Record Dates

2026-05-01