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Study on the effect of PRP on the treatment of urinary incontinenece

Study on the effect of paraurethral injection of platelet rich plasma on the treatment of stress urinary incontinence in women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171201037697N1
Enrollment
20
Registered
2019-01-04
Start date
2017-04-04
Completion date
Unknown
Last updated
2019-01-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

stress urinary incontinence. Stress incontinence (female) (male)

Interventions

Intervention 1: intervention group:blood sampling was done.20ml of intravenous blood was taken on anticoagulant (ACD) and centrifuged in15ml Falcon tubes for 10 minutes at 800 RPM, and after separatio

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
30 Years to 65 Years

Inclusion criteria

Inclusion criteria: Female Existence of Stress urinary incontinence(SUI) symptom Confirm of SUI based on urodinamic test Positive cough stress test Age 30 - 65 Yr No reply to conversative treeatment or intrested in surgical treatment for SUI

Exclusion criteria

Exclusion criteria: post void residual (PVR) more than 100cc evidence of Detrusor overactivity in urodynamic test before surgery Positive history for midurethral sling surgery or any surgery on external genitalia ,bladder, bladder neck or urethra Genitourinary system infection Genitourinary system malignancy Positive history of bleeding disorders or recent anticoagulant treatment Positive recent history of Genitourinary fistula or urethral diverticulum Positive recent history of cyctocele or rectocele Uncontrolled diabetes mellitus Any contraindication for surgery

Design outcomes

Primary

MeasureTime frame
The Severity of urinary incontinence. Timepoint: 0,1,3 month ofter intervention. Method of measurement: International Consultation on Incontinence Questionnaire(ICIQ) , The Questionnaire for Urinary Incontinence Diagnosis(QUID ) , clinical examination( cough stress test).;Quality of Life. Timepoint: 0,1,3 month ofter intervention. Method of measurement: The Incontinence Quality of Life questionnaire(I-QOL).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAtefe eslami

Shiraz University of Medical Sciences

Atefe_eslami70@yahoo.com+98 71 4452 0136

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026