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Negative Pressure Therapy for Groin Wounds

NCT02954835 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 2

Last updated 2020-02-07

No results posted yet for this study

Summary

The purpose of this study is to compare wound infection rates between negative pressure therapy (Prevena) and the traditional sterile dry dressing among patients undergoing vascular surgery involving groin incisions.

Conditions

  • Wound Infection

Interventions

DEVICE

Prevena

Prevena is a sterile silver dressing. On top of the silver dressing is an adhesive plastic, which is connected to a therapy unit through a short length suction tube.

DEVICE

Traditional Dressing

Sterile gauze dressing secured by tape.

Sponsors & Collaborators

  • Englewood Hospital and Medical Center

    lead OTHER

Principal Investigators

  • Thomas Bernik, MD · Englewood Hospital and Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-12-31
Primary Completion
2019-09-03
Completion
2019-09-03

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 NCT02954835 on ClinicalTrials.gov