Clinical Trials Directory

Trials / Completed

CompletedNCT02080546

Vaginal Cuff Dehiscence and Thermal Injury During TLH

Vaginal Cuff Dehiscence and Thermal Injury at the Time of Total Laparoscopic Hysterectomy: A Review of the Duke Experience and Randomized Controlled Trial

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

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.

Conditions

Interventions

TypeNameDescription
PROCEDURECut-CoagIncision 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.
PROCEDUREV-modeIncision 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.
DEVICEValleylab G3000 Electrosurgical DeviceUse of surgical device Valleylab G3000 Electrosurgical Device

Timeline

Start date
2009-12-01
Primary completion
2014-02-01
First posted
2014-03-06
Last updated
2016-06-03
Results posted
2016-06-03

Source: ClinicalTrials.gov record NCT02080546. Inclusion in this directory is not an endorsement.