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Platelet-rich Fibrin Versus HIFU in Management of Stress Urinary Incontinence

Stress Urinary Incontinence Clinical Trial

Official title:
Platelet-rich Fibrin Versus HIFU in Management of Stress Urinary Incontinence

Clinical Trial Summary

Aim of the study is to compare effect of High Intensity Focused Ultrasound (HIFU) and platelet-rich fibrin in management of stress urinary incontinence.

It is a randomized prospective study. After assigning to one of the two groups, patients will undergo relevant treatment.

First group will undergo 3 cycles of intravaginal HIFU treatment in 6-weeks interval.

Second group will undergo 3 injections of platelet-rich fibrin under urethra. Before the treatment and after 2, 6 and 12 months after treatment is finished patients will be asked to fill questionaries concerning quality of life ICIQ-UI SF, ICIQ-LUTS, PISQ12, FSFI.

Before each treatment cycle patients will be examined and asked to fill daily micturition plan.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04144829
Study type Interventional
Source Intima Clinic
Contact Tomasz Basta, PhD
Phone 501295424
Email tomaszbasta@gmail.com
Status Recruiting
Phase N/A
Start date August 1, 2019
Completion date August 1, 2021
View Details
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