Laparoscopic sacropexie: clinical and subjective outcomes in patients with apical genital descent – a retrospective and prospective cohort study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00038856

Enrollment

Registered

2026-01-08

Start date

2021-09-01

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 study, all patients receive sacroplasty using a synthetic mesh for apical prolapse

Eligibility

Sex/Gender

Female

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Sacropexy using the synthetic mesh

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

Measure	Time frame
Recurrence rate of apical prolapse 8 weeks, 6 months, and 12 months after surgery, determined by gynecological examination.	—

Secondary

Measure	Time frame
Complication rate, subjective outcome based on three questionnaires (ICIQ-UI-SF, German pelvic floor questionnaire, and study-specific questionnaire) completed preoperatively, after 8 weeks, and 6 and 12 months postoperatively.	—

Countries

Germany

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 14, 2026