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Clinical Trial Summary

Efficacy of laser therapy in postmenopausal women with symptomatic prolapse stage >1. Assessment tools will include prolapse stage quantification system (POP-Q) and validated condition related questionnaires.


Clinical Trial Description

Postmenopausal women with symptomatic cystocele and/or rectocele stage 2 or 3 will be 1:1 randomly allocated to Er:YAG laser or watchful waiting group. Participants in the Er:YAG laser group will receive laser therapies at monthly intervals, while participants in the watchful waiting group will receive no treatment. All outcomes in both groups will be evaluated at baseline, 4-months and 6-months from baseline. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03714607
Study type Interventional
Source National and Kapodistrian University of Athens
Contact
Status Active, not recruiting
Phase N/A
Start date November 30, 2018
Completion date January 2020

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