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NCT03800615 Clinical Trial

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

Stress Urinary Incontinence Clinical Trial

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03800615
Other study ID # 107183-C
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 9, 2019
Est. completion date February 1, 2019

Study information
Verified date January 2019
Source Far Eastern Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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

Description:

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

Recruitment information / eligibility
Status Completed
Enrollment 1
Est. completion date February 1, 2019
Est. primary completion date February 1, 2019
Accepts healthy volunteers No
Gender Female
Age group 20 Years and older
Eligibility Inclusion Criteria:

- midurethral sling procedure for stress urinary incontinence

- woman with vaginal agenesis.

Exclusion Criteria:

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Cut the sling
Cut the mid-urethral sling for stress urinary incontinence

Locations
Country Name City State
Taiwan Department of Obstetrics and Gynecology, Far-Eastern Memorial Hospital Banqiao New Taipei

Sponsors (1)
Lead Sponsor Collaborator
Far Eastern Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Sexual function Asking the patient whether she can resume sexual intercourse or not after surgery 1 year
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