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OpenTrials
Completed

NCT Number: NCT01246271

Sub Urethral Sling With or With Out Anterior Repair

There is a concern about choosing adequate surgical options for stress urinary incontinence associated with vaginal prolapsed and still lack of evidence can be observed. In this study we compared primary and secondary outcomes of single or combine surgery for SUI with pelvic organ prolapsed.

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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

  • Patients must be female
  • Subjective evidence of stress predominant symptoms on symptom specific questionnaire
  • Stress incontinence on urodynamics
  • Patients must be capable of filling in the symptom diary
  • Prolapse beyond the introitus

Exclusion criteria

  • Patients who are medically unfit to undergo surgical intervention.
  • Patients who have undergone previous continence surgery
  • Patients with voiding dysfunction
  • Patients with recurrent urinary tract infection
  • Patients who are not sure that their family is complete

Treatment and study plan

Primary outcomes

  1. Urinary incontinence cure rate according ICIQ-UIsf

    Time frame: 3 month after surgery

Secondary outcomes

  1. morbidity and complication

    Time frame: 3 month after surgery

Sponsors and collaborators

Lead sponsor

Tabriz University

Other

Registry information

Official study title

a Retrospective Cohort Recognize the Out Comes of SUS With or Without Anterior Vaginal Repair

Important dates

Study start
2008
Primary completion
2009
Study completion
2009
First posted
Nov 23, 2010
Registry last updated
Nov 23, 2010

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.

Published trials that share one or more normalized conditions with this study.