Clinical Trials Directory

Trials / Completed

CompletedNCT01313754

Comparison of Skin Incision Closure Material for the Transobturator Suburethral Sling Procedure

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
160 (actual)
Sponsor
Loma Linda University · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare different skin closure materials for the transobturator suburethral sling procedure. Currently the investigators are using monocryl suture material as the standard for skin closure. This material has anecdotally show to be very irritating to patients who have had this type of surgery. Our study will compare the monocryl suture material with vicryl (polyglactin 910) and dermabond (2-octyl cyanoacrylate) skin glue. The investigators believe that vicryl suture material will be superior in comfort when compared to monocryl and dermabond for this type of procedure.

Conditions

Interventions

TypeNameDescription
PROCEDUREVicryl SutureVicryl suture material will be placed on the patients left sided incision.
PROCEDUREDermabondDermabond skin glue will be placed on the patients left sided incision.

Timeline

Start date
2011-05-01
Primary completion
2012-12-01
Completion
2012-12-01
First posted
2011-03-14
Last updated
2013-01-31

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01313754. Inclusion in this directory is not an endorsement.