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

NCT03105154 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 27

Last updated 2021-02-11

No results posted yet for this study

Summary

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

Conditions

  • Endovascular Procedures

Interventions

OTHER

Prevena Dressing

Prevena dressing is applied on one groin

OTHER

Conventional Dressing

Conventional dressing is applied on the contralateral groin

Sponsors & Collaborators

  • The Cleveland Clinic

    lead OTHER

Principal Investigators

  • Leveser Kirksey · The Cleveland Clinic

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
21 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-02-29
Primary Completion
2020-11-10
Completion
2020-11-10

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03105154 on ClinicalTrials.gov