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Clinical Trials/NCT03225742
NCT03225742
Completed
Not Applicable

The Impact of Postoperative Catheterization Time After Stress Incontinence Surgery to Voiding Dysfunction, Urinary Retention and Success of Surgery

Kanuni Sultan Suleyman Training and Research Hospital1 site in 1 country100 target enrollmentStarted: February 1, 2017Last updated:

Overview

Phase
Not Applicable
Status
Completed
Enrollment
100
Locations
1
Primary Endpoint
early postoperative voiding dysfunction and urinary retention

Overview

Brief Summary

After incontinence surgery, the patients randomly will be divided two groups. In group A postoperative urinary catheterization time will be applied one day, In group B catheterization will be applied two days. After removal of urinary catheter, residual volume will be measured and voiding function will be controlled. In postoperative period; third, sixth month and one year after surgery stress test will be applied to control success of surgery

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
35 Years to 60 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • stress incontinence
  • resistant to medical treatment

Exclusion Criteria

  • had no surgery before
  • has no accompanying uterine descensus
  • has no neurogenic disorder

Outcomes

Primary Outcomes

early postoperative voiding dysfunction and urinary retention

Time Frame: two days

after removal of urinary catheter, has residual volume much more than 150cc (to be measured with urinary catheterization)

Secondary Outcomes

  • The success of stress urinary incontinence surgery(third month, sixth month and one year)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Kerem Doga Seckin

ass prof

Kanuni Sultan Suleyman Training and Research Hospital

Study Sites (1)

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