Patient research anatomy and pessary therapy

Completed

• Conditions: descensus; prolapse; 10029903

• Registration Number: NL-OMON41878
• Lead Sponsor: Medisch Universitair Ziekenhuis Maastricht

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 20

Inclusion Criteria

- Women with an anterior vaginal wall prolaps and/or prolapse of the cervix minimal POP-Q stage II, who are minimal one year treated with pessarytherapy and have no more prolapse complaints and where the pessary shows a good corrections of the prolapse.
- Woman with an anterior vaginal wall prolaps and/or prolapse of the cervix minimal POP-Q stage II, who choose pessarytherapie, but it is not possible to find a pessary that show a good correction of the prolapse and give no more prolapse complaints.

Exclusion Criteria

- Age of 18 years or more
- Patients who are mentally incompetent
- Patients with a posterior vaginal wall prolaps as leading part and where the posterior vaginal wall prolaps the indication is for therapy
- Patients with former prolapse surgery
- Contra-indications for MRI

Study & Design

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

Primary Outcome Measures

Name	Time	Method
<p>Surface of the hiatus<br /><br>Pubococcygeal line, length cervix, transvaginal length, diameter and defect<br /><br>musculus levator ani</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Possible secondary outcomes are: pubococcygeale line, cervix length ,<br /><br>transvaginal length , diameter and defect musculuis levator ani in relation to<br /><br>a standard pessary. The final secondary outcomes, we can not determine yet. The<br /><br>final secondary outcomes will be explored during the analysis of the MRI images<br /><br>.</p><br>