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Recruiting NCT04701047

Prospective Observational Prolapse Study

Trial Parameters

Condition Vaginal Prolapse
Sponsor University Hospital, Ghent
Study Type OBSERVATIONAL
Phase N/A
Enrollment 200
Sex FEMALE
Min Age 18 Years
Max Age N/A
Start Date 2021-09-03
Completion 2028-01
Interventions
vaginal pessaryVaginal prolapse surgery

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: * women with a symptomatic vaginal prolapse * older than 18 years Exclusion Criteria: * 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

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