CompletedNot Applicable

Evaluation of Anatomical Results and Sexual Functions After Unilateral and Bilateral Laparoscopic Suture Sacro-hysteropexy Operations

Turkey (Türkiye)64 participantsStarted 2024-04-05

Plain-language summary

The study was planned as prospective and randomized. For the study, patients will be randomized into two groups as unilateral and bilateral suture sacro-hysteropexy operations.

Who can participate

Age range18 Years – 60 Years

SexFEMALE

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Inclusion criteria

✓. Patients between the ages of 18-60
✓. No previous prolapse surgery
✓. Not having a chronic disease
✓. Having stage 3-4 prolapse

Exclusion criteria

✕. Outside the age range of 18-60 years
✕. Previous prolapse surgery
✕. Having early stage (1-2) prolapse
✕. History of chronic disease

What they're measuring

anatomical success of the operations

Timeframe: changes at 1 and 3 months after surgery

Trial details

NCT IDNCT06341088

SponsorAtaturk University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-11-05

View on ClinicalTrials.gov More Pelvic Organ Prolapse trials