The Effects of Post-Operative Interventions on Surgical Site Occurrences in AWR
Recruiting
N/A
Interventional Study
Abdomen Hernia
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 300 (estimated)
- Sponsor
- Ohio State University · Other
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About This Trial
Randomized controlled trial to compare SSO's in abdominal wall reconstruction patients using Prevena, Prineo, and traditional incisional dressings.
Trial Locations
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Eligibility 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 s…
Contacts