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OpenTrials
Completed

NCT Number: NCT03225742

The Impact of Postoperative Catheterization Time After Stress Incontinence Surgery to Success of Surgery

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

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • stress incontinence
  • resistant to medical treatment

Exclusion criteria

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

Treatment and study plan

to measure the residual volume after catheterization

Diagnostic Test

after first micturition to measure the residual volume in bladder

Primary outcomes

  1. 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

  1. The success of stress urinary incontinence surgery

    Time frame: third month, sixth month and one year

    third, sixth month and one year after surgery, absence of stress urinary incontinence

Sponsors and collaborators

Lead sponsor

Kanuni Sultan Suleyman Training and Research Hospital

Other

Registry information

Official study title

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

Important dates

Study start
2017
Primary completion
2017
Study completion
2018
First posted
Jul 21, 2017
Registry last updated
Feb 20, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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