Trial Comparing Laparoscopic Sacropexy and Vaginal Mesh Surgery for Women Cystocele Repair. (PROSPERE4)
Primary Purpose
Cystocele
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
laparoscopic sacrocolpopexy
vaginal mesh surgery
Sponsored by
About this trial
This is an interventional diagnostic trial for Cystocele
Eligibility Criteria
Inclusion Criteria:
- 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 Criteria:
- 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
Sites / Locations
- Sébatien BLANC
- Hôpital Antoine Béclère
- CHU Estaing
- GCS Flandre Maritime
- CH La Rochelle Service de Gynécologie Obstétrique
- Hôpital BICETRE / Service de Gynécologie Obstétrique
- CHRU de Lille - Service de Gynécologie médico chirurgicale
- CHU de Nîmes
- Groupe Hospitalier Diaconesses Croix St-Simon
- CHI Poissy-St-Germain / Service de gynécologie
- CHU de Poitiers
- Hôpital de Hautepierre
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Other
Arm Label
laparoscopic sacrocolpopexy
vaginal mesh surgery
Arm Description
laparoscopic sacrocolpopexy
vaginal mesh surgery
Outcomes
Primary Outcome Measures
PFDI-20 score
The patient-reported outcome of the intervention will be evaluated using the symptom score calculated using the PFDI-20. It is a self-administered questionnaire on symptoms of prolapse
Secondary Outcome Measures
Full Information
NCT ID
NCT02272361
First Posted
October 20, 2014
Last Updated
July 9, 2019
Sponsor
University Hospital, Lille
1. Study Identification
Unique Protocol Identification Number
NCT02272361
Brief Title
Trial Comparing Laparoscopic Sacropexy and Vaginal Mesh Surgery for Women Cystocele Repair.
Acronym
PROSPERE4
Official Title
Randomized Controlled Trial Comparing Laparoscopic Sacropexy and Vaginal Mesh Surgery for Women Cystocele Repair: Functional and Anatomical Results at Four Years Follow-up
Study Type
Interventional
2. Study Status
Record Verification Date
July 2019
Overall Recruitment Status
Completed
Study Start Date
October 2014 (undefined)
Primary Completion Date
June 20, 2018 (Actual)
Study Completion Date
June 20, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Lille
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
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 cystocele up to 4 years after surgery.
The secondary objectives of this study are the following:
to compare the two techniques for anatomical results based on the clinical evaluation of patients with POP-Q.
to overall quality of life assessment and expectations of patients.
to compare the two techniques for the long-term safety. The evaluation will focus on the adverse effects of long-term sexual and genital symptoms, urinary and digestive functional symptoms, and chronic pelvic pain.
to compare the improvement of the functional outcome assessed by PFDI-20 questionnaire (matched-analysis before versus after).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystocele
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
220 (Actual)
8. Arms, Groups, and Interventions
Arm Title
laparoscopic sacrocolpopexy
Arm Type
Other
Arm Description
laparoscopic sacrocolpopexy
Arm Title
vaginal mesh surgery
Arm Type
Other
Arm Description
vaginal mesh surgery
Intervention Type
Other
Intervention Name(s)
laparoscopic sacrocolpopexy
Intervention Type
Other
Intervention Name(s)
vaginal mesh surgery
Primary Outcome Measure Information:
Title
PFDI-20 score
Description
The patient-reported outcome of the intervention will be evaluated using the symptom score calculated using the PFDI-20. It is a self-administered questionnaire on symptoms of prolapse
Time Frame
4 years
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
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 Criteria:
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Philippe LUCOT, MD,
Organizational Affiliation
University Hospital, Lille
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sébatien BLANC
City
Annecy
ZIP/Postal Code
74374
Country
France
Facility Name
Hôpital Antoine Béclère
City
Clamart
ZIP/Postal Code
92140
Country
France
Facility Name
CHU Estaing
City
Clermont Ferrand
ZIP/Postal Code
63003
Country
France
Facility Name
GCS Flandre Maritime
City
Grande Synthe
ZIP/Postal Code
59760
Country
France
Facility Name
CH La Rochelle Service de Gynécologie Obstétrique
City
La Rochelle
ZIP/Postal Code
17019
Country
France
Facility Name
Hôpital BICETRE / Service de Gynécologie Obstétrique
City
Le Kremlin Bicêtre
ZIP/Postal Code
94275
Country
France
Facility Name
CHRU de Lille - Service de Gynécologie médico chirurgicale
City
Lille
ZIP/Postal Code
59037
Country
France
Facility Name
CHU de Nîmes
City
Nîmes
ZIP/Postal Code
30029
Country
France
Facility Name
Groupe Hospitalier Diaconesses Croix St-Simon
City
Paris
ZIP/Postal Code
75571
Country
France
Facility Name
CHI Poissy-St-Germain / Service de gynécologie
City
Poissy
ZIP/Postal Code
78303
Country
France
Facility Name
CHU de Poitiers
City
Poitiers
ZIP/Postal Code
86000
Country
France
Facility Name
Hôpital de Hautepierre
City
Strasbourg
ZIP/Postal Code
67000
Country
France
12. IPD Sharing Statement
Citations:
PubMed Identifier
23618743
Citation
Lucot JP, Fritel X, Debodinance P, Bader G, Cosson M, Giraudet G, Collinet P, Rubod C, Fernandez H, Fournet S, Lesavre M, Deffieux X, Faivre E, Trichot C, Demoulin G, Jacquetin B, Savary D, Botchorichvili R, Campagne Loiseau S, Salet-Lizee D, Villet R, Gadonneix P, Delporte P, Ferry P, Aucouturier JS, Thirouard Y, de Tayrac R, Fatton B, Wagner L, Nadeau C, Wattiez A, Garbin O, Youssef Azer Akladios C, Thoma V, Baulon Thaveau E, Saussine C, Hermieu JF, Delmas V, Blanc S, Tardif D, Fauconnier A; GROG (groupe de recherche en gynecologie et obstetrique). [PROSPERE randomized controlled trial: laparoscopic sacropexy versus vaginal mesh for cystocele POP repair]. J Gynecol Obstet Biol Reprod (Paris). 2013 Jun;42(4):334-41. doi: 10.1016/j.jgyn.2013.03.012. Epub 2013 Apr 22. French.
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Trial Comparing Laparoscopic Sacropexy and Vaginal Mesh Surgery for Women Cystocele Repair.
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