Clinical Trials Directory

Trials / Completed

CompletedNCT02926924

Prophylactic Application of an Incisional Wound Vac to Prevent Wound Complications in Obese Spine Surgery Patients

Prophylactic Application of an Incisional Wound Vac to Prevent Wound

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
68 (actual)
Sponsor
University of Michigan · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a prospective randomized study evaluating the use of a prophylactic incision wound vac dressing, applied in the OR, on patients undergoing posterior spine surgery with a BMI\>35. Patients are randomized in the operating room to normal postoperative dressing vs. vac dressing. The vac dressing would be left on for 72 hours postoperatively. In the interim, the patients' postoperative care can proceed as usual. Our primary outcomes will be antibiotics or return trip needed to the operating room for wound related complications. The patients only intervention would be the application of an incisional wound vac. The will be no change in the patients postoperative protocol otherwise. This procedure is noninvasive.

Conditions

Interventions

TypeNameDescription
DEVICEWound Vaca therapeutic technique using a vacuum dressing to promote healing in acute or chronic wounds and enhance healing of first and second degree burns.
OTHERStandard Dressingstandard dressing with drain tube and bandage

Timeline

Start date
2011-08-01
Primary completion
2015-01-15
Completion
2015-01-15
First posted
2016-10-06
Last updated
2025-04-11
Results posted
2025-04-11

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02926924. Inclusion in this directory is not an endorsement.