Actively Recruiting
Role of Mesh in Laparoscopic Sacropexy Surgical Techniques for the Treatment of Female Genital Prolapse
Led by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Updated on 2024-12-06
160
Participants Needed
2
Research Sites
12 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aims to determine the rate of recurrence of central pelvic organ prolapse in patients who have undergone surgery (sacropexy with and without mesh) for the same pathology.
CONDITIONS
Official Title
Role of Mesh in Laparoscopic Sacropexy Surgical Techniques for the Treatment of Female Genital Prolapse
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Clinical diagnosis of genital prolapse stage 2 or higher according to POP-Q classification
- Female patients undergoing laparoscopic sacropexy surgery with mesh (group 1) or without mesh (group 2)
- Provided informed consent
- At least one follow-up evaluation at 24 months after surgery
You will not qualify if you...
- Age over 80 years
- Previous genital prolapse surgery
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Bologna, Bologna, Italy, 40138
Actively Recruiting
2
Azienda Ospedaliera Universitaria Integrata di Verona
Verona, Verona, Italy, 37126
Not Yet Recruiting
Research Team
D
Diego Raimondo, MD
CONTACT
M
Manuela Maletta, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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