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Burch colposuspension for stress urinary incontinence in women – results of a clinical trial

Burch colposuspension for stress urinary incontinence in women – results of a clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00037464
Enrollment
100
Registered
2025-07-17
Start date
2023-12-01
Completion date
Unknown
Last updated
2025-10-06

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: An estimated 10–40% of all women experience urinary incontinence at some point in their lives, with prevalence increasing with age. Colposuspension (here always referring to Burch colposuspen

Sponsors

Universitätsfrauenklinik Bonn
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients > 18 years of age eligible for consent who have undergone colposuspension in the Urogynecology Department of the Women's Hospital at the University Hospital Bonn since 2020 are included.

Exclusion criteria

Exclusion criteria: Patients who do not meet the inclusion criteria or who cannot speak/write/read German.

Design outcomes

Primary

MeasureTime frame
The primary objective is to record the subjective and objective outcomes after colposuspension and thus determine the value of colposuspension today - Subjective: Success rate based on three questionnaires, which the patients complete once again - Objective: Urogynecological status incl. POP-Q based on routine urogynecological examinations and sonography; pre- and postoperative findings are compared

Secondary

MeasureTime frame
Survey of a wound infection rate with possible risk factors, survey of an in-house success rate of colposuspension for the treatment of stress incontinence.

Countries

Germany

Contacts

Public ContactCarolin Schröder

Universitätsfrauenklinik Bonn

carolin.schroeder@ukbonn.de004915116858134

Outcome results

None listed

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