Skip to content

Primary treatment of vaginal prolapse, pessary use versus prolapse surgery. A comparison of quality of life.

Primary treatment of vaginal prolapse, pessary use versus prolapse surgery. A comparison of quality of life. - Pessary versus prolaps surgery

Status
Active, not recruiting
Phases
Phase 2
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON33706
Enrollment
80
Registered
2009-09-14
Start date
2009-10-01
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

prolapse

Interventions

None listed

Sponsors

Máxima Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Vaginal prolapse stage 2-4 (POP-Q criteria, ICS).

Exclusion criteria

Exclusion criteria: Prolapse surgery of incontinence surgery in the history

Design outcomes

Primary

MeasureTime frame
The primary outcome will be disease specific quality of life, as measured with the urogenital distress inventory (UDI).

Secondary

MeasureTime frame
Secondary outcomes will be women*s perceived improvement in the prolapse symptoms, clinicians grading of prolapse at one year of follow-up.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)