Multicenter Study on the Correction of Prolapse Via Laparoscopy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorFundacion para la Formacion e Investigacion Sanitarias de la Region de Murcia

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 sacropexy.

Eligibility criteria

Qualifiers

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.

Disqualifiers

History of abdominal prolapse reconstructive surgery.

History of prolapse reconstructive surgery with vaginal meshes.

Stage I according to the POP-Q classification or asymptomatic prolapse.

Medical contraindication for general anaesthesia.

Trial design

Treatments tested in this trial

  • lateral laparoscopic suspension (LLS)
  • Sacropexy without posterior mesh fixation on the puborrectalis muscle

Treatment groups

181 Participants
are divided into 2 treatment groups