Clinical Trials Directory

Trials / Terminated

TerminatedNCT03010137

Incisional Negative Pressure Wound Therapy in High Risk Patients Undergoing Panniculectomy: A Prospective Randomized Controlled Trial

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
30 (actual)
Sponsor
University of California, Davis · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Incisional negative pressure therapy (INPWT) has previously been shown in certain patient populations to decrease wound healing complications, decrease the rate of hematomas and seromas, as well as have better scar quality. We have found a group of patients, those who have panniculectomies in preparation for renal transplant, with significantly higher rates of wound healing complications. We believe the best way to demonstrate benefits of incisional negative pressure wound therapy will be in this group of patients known to have significantly higher rates of wound complications.

Conditions

Interventions

TypeNameDescription
PROCEDUREIncisional Negative Pressure Wound Therapy
PROCEDUREStandard Closure with Skin Glue
DEVICEPICO (Smith&Nephew)Off the shelf, disposable negative pressure wound therapy device. Contains sterile dressing as well as an attached small (pager sized) suction device/canister.
DEVICEDermabondFinal wound closure with skin glue.

Timeline

Start date
2015-12-01
Primary completion
2019-03-13
Completion
2019-03-13
First posted
2017-01-04
Last updated
2020-06-09
Results posted
2020-06-09

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03010137. Inclusion in this directory is not an endorsement.