Replacement of synthetic mesh by an autograft in descensus surgery.

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00015480

Enrollment

100

Registered

2018-09-05

Start date

2018-09-24

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

N81.8

Interventions

Group 1: The tendon of the semitendinosus muscle should replace a synthetic mesh in patients with pelvic organ prolapse. With this investigation the feasibility for it has 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 pelvic organ prolapse.

Exclusion criteria

Exclusion criteria: Patients in whom the tendon of the semitendinosus muscle was 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;Bernd Hornemann;Holthaus

Krankenhaus Sachsenhausen;St. Elisabeth Krankenhaus Damme

ahornemann@khs-ffm.de;holthaus@krankenhaus-damme.de00496966051141;05491-601

Outcome results

None listed

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