Replacement of synthetic meshes with endogenous tissue.

Phase 4

• Conditions: N39.3; Stress incontinence

• Registration Number: DRKS00015481
• Lead Sponsor: niversitätsfrauenklinik Mannnheim

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2018-09-19
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Female
• Target Recruitment: 5

Inclusion Criteria

Patients with the indication for surgical treatment of stress urinary incontinence.

Exclusion Criteria

Patients in whom the tendons of the semitendinosus muscles were otherwise used.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The feasibility should be checked. The duration of the operation, blood loss and possibly complications are measured

Secondary Outcome Measures

Name	Time	Method
Satisfaction of the patient<br>Success control after 3 and 6 months