CompletedPhase 4

A Randomized Clinical Trial Evaluating Negative Pressure Therapy to Decrease Vascular Groin Incision Complications

United States140 participantsStarted 2015-01

Plain-language summary

The purpose of this study is to determine if the application of a negative pressure dressing intraoperatively (Prevena; KCI, Inc) to vascular groin incisions decreases the wound complication rate in high risk patients.

Who can participate

Age range18 Years – 100 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * All patients undergoing a femoral incision during vascular reconstruction or repair will be considered for study Exclusion Criteria: * Emergency procedure * Unable to give informed consent

What they're measuring

Groin Wound Complication

Timeframe: 30 days

Trial details

NCT IDNCT02581904

SponsorThomas Jefferson University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2016-12

Results submitted2026-02-06

View on ClinicalTrials.gov More Wound Infection trials