Replacement of synthetic meshes with endogenous tissue.

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

DRKS

Registry ID

DRKS00015481

Enrollment

Registered

2018-09-19

Start date

2018-10-15

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

N39.3

Interventions

Group 1: The tendon of the semintendinosus muscle should replace a plastic net in the treatment of female stress urinary incontinence. With this investigation the feasibility for it is to be shown.

Eligibility

Sex/Gender

Female

Age

18 Years to No maximum

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

Measure	Time frame
The feasibility should be checked. The duration of the operation, blood loss and possibly complications are measured	—

Secondary

Measure	Time frame
Satisfaction of the patient Success control after 3 and 6 months	—

Countries

Germany

Contacts

Public ContactAmadeus Hornemann

Universitätsfrauenklinik Mannnheim

amadeus.hornemann@umm.de00496213832286

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026