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Multicenter Study on the Correction of Prolapse Via Laparoscopy

RecruitingNAAges 18 Years - anyFemaleFundacion para la Formacion e Investigacion Sanit…
NCT06815731 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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.

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📋 Eligibility rules (as published)
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 prolapse reconstructive surgery with vaginal meshes. * Stage I according to the POP-Q classification or asymptomatic prolapse. * Medical contraindication for general anaesthesia. * Patient preference for vaginal surgical treatment. * Patient does not wish to participate in the study.
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What it tests

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

1 site
HCUVA
Murcia, Spain
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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