Investigating the effect of platelet rich plasma (PRP) injection in women with stress urinary incontinence

Phase 3

• Conditions: Other specified urinary incontinence; N39.49; Stress urinary incontinence.

• Registration Number: IRCT20221208056749N1
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Pending
• Sex: Female
• Target Recruitment: 60

Inclusion Criteria

Women over 20 years
Moderate to mild stress urinary incontinence
Diagnosing stress urinary incontinence based on history, physical examination and questionnaire
Failure to respond to medical treatments for stress urinary incontinence
Written informed consent to participate in the present study

Exclusion Criteria

Existence of detrusor hyperactivity in urodynamics
History of stress urinary incontinence surgery
Urinary tract infection
Obesity (BMI greater than 30)

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: One month, 3 months, 6 months and 12 months after surgery. Method of measurement: Visual Analogue Scale.;Amount of urine leakage. Timepoint: One month, 3 months, 6 months and 12 months after surgery. Method of measurement: Urinary distress inventory (UDI-6).;Frequency of urinary leakage. Timepoint: One month, 3 months, 6 months and 12 months after surgery. Method of measurement: Incontinence Questionnaire–Urinary Incontinence Short Form (ICIQ-UI SF).