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

N/A
Waitlist Available
Led By Leveser Kirksey
Research Sponsored by The Cleveland Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 30 days
Awards & highlights
No Placebo-Only Group

Summary

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

Eligible Conditions
  • Endovascular Procedures

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~30 days
This trial's timeline: 3 weeks for screening, Varies for treatment, and 30 days for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
% of infection at 30 days

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Prevena DressingExperimental Treatment1 Intervention
Groin dressed with Prevena
Group II: Conventional DressingActive Control1 Intervention
Groin dressed with conventional bandage

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Who is running the clinical trial?

The Cleveland ClinicLead Sponsor
1,057 Previous Clinical Trials
1,371,445 Total Patients Enrolled
Leveser KirkseyPrincipal InvestigatorThe Cleveland Clinic
~3 spots leftby Dec 2025
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