Prospective Observational Prolapse Study

Recruiting now

Conditions studied: Vaginal Prolapse

In brief

The rationale of the study is to investigate the results of a prolapse treatment in adult women with a vaginal prolapse. The investigators will investigate this by taking questionnaires in women undergoing a surgical prolapse repair and in women that are being treated by a vaginal pessary. The objective is to compare the results of the different methods with each other and to observe the evolution of the symptoms in patients undergoing surgery or pessary use. The investigators would also like to discover existing problems in pessary use and adverse effects.

Key facts

Study ID

NCT04701047

Run by

University Hospital, Ghent

People needed

200

Starts

2021-09-03

Expected to finish

2028-01-01

Last updated by the study team

2025-01-15

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• women with a symptomatic vaginal prolapse
• older than 18 years

You may not qualify if…

• under 18 years old
• undergone a previous treatment with a pessary or surgery for vaginal prolapse
• contra-indications for surgery or pessary use
• active or passive child wish
• not able to understand the Dutch language
• not able to give a written consent

Where it is running

• Ghent University Hospital — Ghent, Belgium (enrolling)

Full record on ClinicalTrials.gov

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