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Clinical Trials/NCT04071288
NCT04071288
Completed
Not Applicable

Comparison of Burch Colposuspension and Mid-urethral Sling Operations for Stress Urinary Incontinence

Kanuni Sultan Suleyman Training and Research Hospital1 site in 1 country50 target enrollmentJanuary 1, 2017
ConditionsIncontinence

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Incontinence
Sponsor
Kanuni Sultan Suleyman Training and Research Hospital
Enrollment
50
Locations
1
Primary Endpoint
recurrence
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Stress urinary incontinence is common in women. the treatment of this condition is surgery. investigators add stress incontinence surgery to patients who undergo total laparoscopic hysterectomy for benign reasons.

Depending on the patient's general condition and indications, the operation can be performed by vaginal approach, as well as mid-urethral sling operations and laparoscopic burch colposuspension.

The researchers aimed to compare these two types of operations performed on patients. In this way, the superiority and disadvantage of each other in two procedures will be demonstrated.

Registry
clinicaltrials.gov
Start Date
January 1, 2017
End Date
January 1, 2020
Last Updated
6 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Pınar Kadirogulları

pınar kadiroğulları M.D, Department of Obstetrics and Gynecology

Kanuni Sultan Suleyman Training and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • A total laparoscopic hysterectomy was planned for benign causes,
  • Patients scheduled for simultaneous operation for incontinence

Exclusion Criteria

  • Patients previously operated for urinary incontinence
  • Patients whose diagnosis of stress urinary incontinence is uncertain
  • Patients with urinary tract infection

Outcomes

Primary Outcomes

recurrence

Time Frame: 2 years

in patients who underwent total laparoscopic hysterectomy and simultaneous incontinence surgery for benign reasons; In the early postoperative period, relapse will be evaluated at 1 month, 6 months and 12 months.

Study Sites (1)

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