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Prospective Observation of Wound Healing With Prevena Incision Management System

NCT01704924 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2018-01-19

No results posted yet for this study

Summary

This study aims to assess the quality of wound healing in abdominal scars with and without the Prevena Incision Management System. The hypothesis is that Prevena will lead to improved wound healing with less swelling, bruising, and inflammation, as well as less potential for infection, seroma, and dehiscence.

Conditions

  • Scarring

Interventions

DEVICE

Prevena

Device will be applied at end of procedure over closed incision

PROCEDURE

Standard of Care Dressing

Dressing applied as Standard of Care

Sponsors & Collaborators

  • University of California, Irvine

    lead OTHER

Principal Investigators

  • Gregory Evans, MD · The University of California Irvine

Study Design

Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-10-31
Primary Completion
2016-12-31
Completion
2016-12-31

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 NCT01704924 on ClinicalTrials.gov