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Vaginal Cuff Closure Time Using Unidirectional Barbed Suture in Robotic Hysterectomy

NCT01814579 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2013-03-26

No results posted yet for this study

Summary

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

Conditions

  • Disease (or Disorder); Gynecological

Interventions

DEVICE

Unidirectional 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.

DEVICE

polyglactin 910 (Vicryl)

Patients in the Smooth Suture arm will have their vaginal cuff closed with this device during their robotic hysterectomy.

Sponsors & Collaborators

  • Methodist LeBonheur Hospital System

    collaborator UNKNOWN

  • The West Clinic

    collaborator UNKNOWN

  • University of Tennessee

    lead OTHER

Principal Investigators

  • Todd Tillmanns, MD · University of Tennessee, The West Clinic

  • Adam Mabe, MD · University of Tennessee

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-07-31
Primary Completion
2013-05-31
Completion
2013-08-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01814579 on ClinicalTrials.gov