Clinical Trials Directory

Trials / Unknown

UnknownNCT01814579

Vaginal Cuff Closure Time Using Unidirectional Barbed Suture in Robotic Hysterectomy

Vaginal Cuff Closure Time Using Unidirectional Barbed Suture in Robotic Hysterectomy, a Randomized Controlled Trial

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
University of Tennessee · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is designed to determine if using the V-Loc Wound Closure System expedites operative time in robotic hysterectomy.

Detailed description

Currently both traditional continuous smooth suture and unidirectional barbed suture techniques are standard of care in robotic hysterectomy and the decision of which to use is at the discretion of the surgeon. By using unidirectional barbed suture in which no knot tying is required, wound closure time may be decreased resulting in decreased operative time. This study was created to compare vaginal cuff closure times using these two techniques.

Conditions

Interventions

TypeNameDescription
DEVICEUnidirectional Barbed Suture (V-Loc)Patients enrolled in the Unidirectional Barbed Suture arm will have their vaginal cuff closed using this device during their robotic hysterectomy.
DEVICEpolyglactin 910 (Vicryl)Patients in the Smooth Suture arm will have their vaginal cuff closed with this device during their robotic hysterectomy.

Timeline

Start date
2012-07-01
Primary completion
2013-05-01
Completion
2013-08-01
First posted
2013-03-20
Last updated
2013-03-26

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01814579. Inclusion in this directory is not an endorsement.