Prospective Observational Prolapse Study
ConditionVaginal Prolapse
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorUniversity Hospital, Ghent
About this trial
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
Qualifiers
women with a symptomatic vaginal prolapse
older than 18 years
Disqualifiers
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
Trial design
Treatments tested in this trial
- vaginal pessary
- Vaginal prolapse surgery
Treatment groups
200 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov