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Vaginal Cuff Dehiscence and Thermal Injury During TLH

Primary Purpose

Vaginal Cuff Dehiscence, Thermal Injury

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Cut-Coag
V-mode
Valleylab G3000 Electrosurgical Device
Sponsored by
Duke University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Vaginal Cuff Dehiscence focused on measuring Vaginal cuff dehiscence, Thermal Injury, Total laparoscopic hysterectomy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age ≥18 years
  2. Patient scheduled for total laparoscopic hysterectomy (TLH)
  3. Signed informed consent

Exclusion Criteria:

1. Known pelvic infection within 30 days prior to hysterectomy

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Experimental

    Arm Label

    Cut/Coag

    V-mode

    Arm Description

    Outcomes

    Primary Outcome Measures

    Degree of Thermal Injury at the Time of Laparoscopic Hysterectomy
    distance in millimeters over which thermal tissue injury extends (henceforth referred to as "injury").

    Secondary Outcome Measures

    Incidence of Clinical Surrogates of Compromised Vaginal Cuff Healing
    a difference between arms in the proportion of patients who have at least one of the following post-operatively: vaginal vault granulation tissue, vaginal cuff separation/dehiscence, or vaginal apex infection

    Full Information

    First Posted
    March 3, 2014
    Last Updated
    April 28, 2016
    Sponsor
    Duke University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02080546
    Brief Title
    Vaginal Cuff Dehiscence and Thermal Injury During TLH
    Official Title
    Vaginal Cuff Dehiscence and Thermal Injury at the Time of Total Laparoscopic Hysterectomy: A Review of the Duke Experience and Randomized Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2016
    Overall Recruitment Status
    Completed
    Study Start Date
    December 2009 (undefined)
    Primary Completion Date
    February 2014 (Actual)
    Study Completion Date
    undefined (undefined)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Duke University

    4. Oversight

    5. Study Description

    Brief Summary
    Purpose of this randomized control study is to determine if the mode of electrothermal colpotomy incision affects (1) the degree of thermal injury at the time of laparoscopic hysterectomy or (2) the incidence of clinical surrogates of compromised vaginal cuff healing. Women already scheduled for TLH will be randomized to colpotomy incision with the V mode or standard cut/coag form of electrothermal energy. Prevalence of vaginal cuff injury will be calculated, and cross tabulation tables will be used to examine the association fo dehiscence with proposed risk factors in the retrospective part of the study. In the randomized controlled trial, depth of thermal injury will be compared between the two groups, and a chi-square test will be used to test for a difference in clinical outcomes between the two groups. There is little risk associated with this study above the normal surgical risks; however, the V mode has not been previously been studied for its use in making a colpotomy incision. Loss of confidentiality is a risk of the study, but all samples will be de-identified and given a unique study number, and only individuals directly involved in the study will be given access to the study information.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Vaginal Cuff Dehiscence, Thermal Injury
    Keywords
    Vaginal cuff dehiscence, Thermal Injury, Total laparoscopic hysterectomy

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    120 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Cut/Coag
    Arm Type
    Active Comparator
    Arm Title
    V-mode
    Arm Type
    Experimental
    Intervention Type
    Procedure
    Intervention Name(s)
    Cut-Coag
    Other Intervention Name(s)
    Valleylab G3000 Electrosurgical Device
    Intervention Description
    Incision using electrothermal cautery, with an attempt made to use the "cut" (continuous low-voltage, high-current) for colpotomy incision following the initial scoring of the cervico-vaginal tissue on the "coag" (pulsed high-voltage, low-current) mode.
    Intervention Type
    Procedure
    Intervention Name(s)
    V-mode
    Other Intervention Name(s)
    Valleylab G3000 Electrosurgical Device
    Intervention Description
    Incision using electrothermal cautery in the "V mode". The V mode combines real-time tissue sensing technology with the cut and coag waveforms to reduce the amount of thermal spread to the tissue without sacrificing hemostasis during monopolar electrothermal procedures.
    Intervention Type
    Device
    Intervention Name(s)
    Valleylab G3000 Electrosurgical Device
    Intervention Description
    Use of surgical device Valleylab G3000 Electrosurgical Device
    Primary Outcome Measure Information:
    Title
    Degree of Thermal Injury at the Time of Laparoscopic Hysterectomy
    Description
    distance in millimeters over which thermal tissue injury extends (henceforth referred to as "injury").
    Time Frame
    up to 36 months
    Secondary Outcome Measure Information:
    Title
    Incidence of Clinical Surrogates of Compromised Vaginal Cuff Healing
    Description
    a difference between arms in the proportion of patients who have at least one of the following post-operatively: vaginal vault granulation tissue, vaginal cuff separation/dehiscence, or vaginal apex infection
    Time Frame
    4 weeks, 3 months, and 6 months after hysterectomy for a post-operative check and pelvic examination

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Age ≥18 years Patient scheduled for total laparoscopic hysterectomy (TLH) Signed informed consent Exclusion Criteria: 1. Known pelvic infection within 30 days prior to hysterectomy
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Paula S Lee, MD
    Organizational Affiliation
    Duke University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    25305572
    Citation
    Teoh D, Lowery WJ, Jiang X, Ehrisman J, Halvorson P, Broadwater G, Bentley R, Secord AA, Sobolewski C, Berchuck A, Havrilesky LJ, Valea FA, Lee PS. Vaginal cuff thermal injury by mode of colpotomy at total laparoscopic hysterectomy: a randomized clinical trial. J Minim Invasive Gynecol. 2015 Feb;22(2):227-33. doi: 10.1016/j.jmig.2014.10.002. Epub 2014 Oct 8.
    Results Reference
    derived

    Learn more about this trial

    Vaginal Cuff Dehiscence and Thermal Injury During TLH

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