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

Phase 2

Completed

• Conditions: prolapse; 10029903

• Registration Number: NL-OMON33706
• Lead Sponsor: Máxima Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 80

Inclusion Criteria

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

Exclusion Criteria

Prolapse surgery of incontinence surgery in the history

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The primary outcome will be disease specific quality of life, as measured with<br /><br>the urogenital distress inventory (UDI). </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary outcomes will be women*s perceived improvement in the prolapse<br /><br>symptoms, clinicians grading of prolapse at one year of follow-up. </p><br>