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
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
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
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
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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