Laparoscopic Lateral Mesh Suspension for Pelvic Organ Prolapse

Status Completed

Clinical Trial Summary

This study is aimed to share our clinical experience in an uterine-preserving laparoscopic lateral suspension of apical prolapses with mesh operation after minor modifications in technique. Transperineal ultrasonography and several questionnaires are used for objective and subjective outcomes.

Clinical Trial Description

Vaginal length, bladder neck mobility and pelvic floor biometry with anteroposterior hiatal diameter and pelvic organ descent measurements are measured by transperineal ultrasonography to assess anatomic success in the preoperative and at postoperative 18th months if available.

Female Sexual Function Index (FSFI), Michigan Incontinence Severity Index (M-ISI), Prolapse Quality of Life questionnaire (PQoL), Pelvic Organ Prolapse Symptom Score (POP-SS) and Visual Analog Score (VAS) are used to assess subjective success in the preoperative and at postoperative 18th months if available. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03387202
Study type	Observational [Patient Registry]
Source	Fatih Sultan Mehmet Training and Research Hospital
Contact
Status	Completed
Phase	N/A
Start date	November 1, 2016
Completion date	February 5, 2018

View Details

See also
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