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Replacement of synthetic mesh by an autograft in descensus surgery.

Not Applicable
Recruiting
Conditions
N81.8
Other female genital prolapse
Registration Number
DRKS00015480
Lead Sponsor
Arbeitsgemeinschaft Gynäkologische Endoskopie
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
100
Inclusion Criteria

Patients with the indication for surgical treatment of pelvic organ prolapse.

Exclusion Criteria

Patients in whom the tendon of the semitendinosus muscle was otherwise used.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The feasibility should be checked. The duration of the operation, blood loss and possibly complications are measured.
Secondary Outcome Measures
NameTimeMethod
Satisfaction of the patient<br>Success control after 3 and 6 months
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