Status:
COMPLETED
Trial Comparing Laparoscopic Sacropexy and Vaginal Mesh Surgery for Women Cystocele Repair.
Lead Sponsor:
University Hospital, Lille
Conditions:
Cystocele
Eligibility:
FEMALE
45-75 years
Phase:
NA
Brief Summary
The primary objective of this study is to compare with PFDI-20 questionnaire the functional outcome of laparoscopic sacrocolpopexy and vaginal mesh surgery in the treatment of symptomatic exteriorised...
Eligibility Criteria
Inclusion
- All the patients included in the PROSPERE study will be included in the PROSPERE-4 study. The inclusion criterias for the PROSPERE study are:
- Written informed consent
- insured under the French social security system
Exclusion
- Unwillingness or inability to comply with the requirements of this protocol, including the presence of any condition (physical, mental, or social) that is likely to affect the subject's ability to comply with the study protocol
- Participation in another trial
Key Trial Info
Start Date :
October 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 20 2018
Estimated Enrollment :
220 Patients enrolled
Trial Details
Trial ID
NCT02272361
Start Date
October 1 2014
End Date
June 20 2018
Last Update
July 11 2019
Active Locations (12)
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1
Sébatien BLANC
Annecy, France, 74374
2
Hôpital Antoine Béclère
Clamart, France, 92140
3
CHU Estaing
Clermont-Ferrand, France, 63003
4
GCS Flandre Maritime
Grande-Synthe, France, 59760