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

• Sponsor: Far Eastern Memorial Hospital (Other)
• Overall Status: Completed
• CT.gov ID: NCT03800615
• Collaborator: (none)
• Enrollment: 1
• Location: 1
• Actual Duration (Days): 23
• Patients Per Site Per Month: 1.3

Study Details

Study Description

Brief Summary

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

Condition or Disease	Intervention/Treatment	Phase
Stress Urinary Incontinence; Vaginal Agenesis	Procedure: Cut the sling

Detailed Description

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

Study Design

• Study Type: Observational
• Actual Enrollment: 1 participants
• Observational Model: Case-Only
• Time Perspective: Retrospective
• Official Title: Iatrogenic Impairment of Urethral Coitus Owing to Midurethral Sling Procedure in a Woman With Vaginal Agenesis.
• Actual Study Start Date: Jan 9, 2019
• Actual Primary Completion Date: Feb 1, 2019
• Actual Study Completion Date: Feb 1, 2019

Outcome Measures

Primary Outcome Measures

1. Sexual function [1 year]

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

Eligibility Criteria

Criteria

• Ages Eligible for Study: 20 Years and Older
• Sexes Eligible for Study: Female
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• midurethral sling procedure for stress urinary incontinence

• woman with vaginal agenesis.

Exclusion Criteria:

• Nil

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Department of Obstetrics and Gynecology, Far-Eastern Memorial Hospital	Banqiao	New Taipei	Taiwan	22050

Sponsors and Collaborators

• Far Eastern Memorial Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Sheng-Mou Hsiao, Chief, Department of Obstetrics & Gynecology, Far Eastern Memorial Hospital
• ClinicalTrials.gov Identifier: NCT03800615
• Other Study ID Numbers: 107183-C
• First Posted: Jan 11, 2019
• Last Update Posted: Mar 8, 2019
• Last Verified: Jan 1, 2019

• Individual Participant Data (IPD) Sharing Statement: Undecided
• Plan to Share IPD: Undecided
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Additional relevant MeSH terms: Urinary Incontinence; Urinary Incontinence, Stress; Congenital Abnormalities

Study Results

No Results Posted as of Mar 8, 2019