Groin Wound Infection Rate Using Prevena Compared to Standard Dressing in Vascular Surgery Patients With High Risk

Completed · Not applicable

Conditions studied: Endovascular Procedures

In brief

Evaluate wound healing using Prevena compared to standard dressings in high risk patients after vascular surgery.

Key facts

Study ID

NCT03105154

Run by

The Cleveland Clinic

People needed

27

Starts

2016-02-01

Expected to finish

2020-11-10

Last updated by the study team

2021-02-11

Who can join

Age: 21 and older, up to 100. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients with known bilateral vascular peripheral disease who are being evaluated for possible bilateral femoral endarterectomy
• Patients with one or more risk factor (diabetes mellitus, Obesity, heavy smoker, immunodeficiency disease, groin reoperation, prosthetic)
• Patients in follow-up at Clinic in the Vascular Surgery Department
• Sign of informed consent
• English speaking

You may not qualify if…

• Refusal to participate
• pregnancy
• unilateral femoral endarterectomy
• subjects for whom Prevena IMS is contraindicated

Where it is running

• Clevealnd Clnic — Cleveland, Ohio, United States

Full record on ClinicalTrials.gov

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