Multicenter Study on the Correction of Prolapse Via Laparoscopy
Recruiting
N/A
Interventional Study
Pelvic Floor Disorders
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 181 (estimated)
- Sponsor
- Fundacion para la Formacion e Investigacion Sanitarias de la Region de Murcia · Other
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About This Trial
In the laparoscopic lateral suspension (LLS) technique, the fixation of the mesh as a prosthetic element for correcting anterior apical vaginal prolapse at the level of the dome or uterus can offer anatomical and functional results that are not inferior to those of the conventional surgical technique, minimize possible intraoperative complications and facilitate the specific learning curve of sacr…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patients with Stage II- IV primary or recurrent prolapse affecting the anterior or middle vaginal compartment with or without minimal posterior defect (Stage I) according to the POP-Q.
Exclusion Criteria:
* History of abdominal prolapse reconstructive surgery.
* History of p…
Contacts