Clinical Trials Directory

Trials / Terminated

TerminatedNCT02302222

The Management of Closed Surgical Incisions Resulting From Incisional Hernia Repair and/or Functional Panniculectomy Using the Prevena™ Customizable™ Dressing

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
71 (actual)
Sponsor
KCI USA, Inc · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this study is to evaluate the impact of Customizable in the management of extensive closed surgical incisions for Subjects undergoing abdominal surgery for incisional hernia repair and/or functional panniculectomy as compared to SOC dressing, and to significantly reduce the SSC rate experienced by Subjects receiving Customizable vs. SOC surgical incision dressing.

Conditions

Interventions

TypeNameDescription
DEVICECustomizable Dressing with ActiV.A.C. Therapy Unit
DEVICEStandard of Care Dressing

Timeline

Start date
2015-05-01
Primary completion
2017-07-31
Completion
2017-07-31
First posted
2014-11-26
Last updated
2024-10-16
Results posted
2018-12-12

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT02302222. Inclusion in this directory is not an endorsement.