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OpenTrials
Completed

NCT Number: NCT03800615

Iatrogenic Impairment of Urethral Coitus Owing to Midurethral Sling Procedure in a Woman With Vaginal Agenesis.

To report a case of impairment urethral coitus after the midurethral sling procedure

Completed

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Key information

About this study

To report a case of impairment urethral coitus after the midurethral sling procedure.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • midurethral sling procedure for stress urinary incontinence
  • woman with vaginal agenesis.

Exclusion criteria

  • Nil

Treatment and study plan

Cut the sling

Procedure

Cut the mid-urethral sling for stress urinary incontinence

Primary outcomes

  1. Sexual function

    Time frame: 1 year

    Asking the patient whether she can resume sexual intercourse or not after surgery

Sponsors and collaborators

Lead sponsor

Far Eastern Memorial Hospital

Other

Registry information

Important dates

Study start
2019
Primary completion
2019
Study completion
2019
First posted
Jan 11, 2019
Registry last updated
Mar 8, 2019

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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