Registry study on the use of the semitendinosus tendon in patients with pelvic organ prolapse

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00038855

Enrollment

1000

Registered

2026-01-05

Start date

2023-03-01

Completion date

Unknown

Last updated

2026-01-12

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

Conditions

N81.9

Interventions

Group 1: Single-arm registry study, all patients with apical prolapse undergo sacropexy with use of the semitendinosus tendon

Eligibility

Sex/Gender

Female

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 18 years old, apical prolapse at least grade I, sacropex with use of the semitendinosus tendon

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

Measure	Time frame
Primary Outcome: recurrence rate of apical prolapse 3 and 12 months postoperatively, assessed by gynecological examination	—

Secondary

Measure	Time frame
Perioperative complication rate, change in subjective perception of bladder, bowel, prolapse symptoms, and sexuality by completing the German Pelvic Floor Questionnaire preoperatively and 3 and 12 months postoperatively	—

Countries

Austria, Germany, Switzerland

Contacts

Public ContactDominique Könsgen-Mustea

Universitätsklinik Bonn, Frauenklinik

carolin.schroeder@ukbonn.de0228 287 15444

Outcome results

None listed

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