Vaginal Cuff Dehiscence at Total Laparoscopic Hysterectomy
Not Applicable
Completed
- Conditions
- Surgical Wound Dehiscence
- Interventions
- Device: Monopolar needle electrode
- Registration Number
- NCT02879487
- Lead Sponsor
- Ankara University
- Brief Summary
The aim of this study is to assess a major complication of total laparoscopic hysterectomy, vaginal dehiscence, with two different colpotomy techniques. With this aim patients to be operated for laparoscopic hysterectomy will be randomized to two different techniques. The colpotomy will be undertaken by 'cut mode' in the first group and 'coagulation mode' in the second group. All of the operations will be preformed by the same surgical at a university hospital. Vaginal dehiscence after surgery is the primary outcome measure.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 200
Inclusion Criteria
- All total laparoscopic hysterectomies performed by a single surgeon
- Both benign and malignant cases
- Completed laparoscopically
- Intracorporeal vaginal cuff suturing
Exclusion Criteria
- Robotic hysterectomies
- Pelvic infection within 30 days before surgery
- Conversion to laparotomy
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Coagulation mode Monopolar needle electrode Colpotomy will be performed by monopolar needle electrode using coagulation mode Cut mode Monopolar needle electrode Colpotomy will be performed by monopolar needle electrode using cut mode
- Primary Outcome Measures
Name Time Method Vaginal dehiscence 3 months Vaginal dehiscence up to 3 months after surgery
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Ankara University Medical Faculty Hospital
🇹🇷Ankara, Turkey