Actively Recruiting
PRP & PDO Threads in Treatment of Stress Incontinence
Led by Al-Azhar University · Updated on 2025-03-20
10
Participants Needed
1
Research Sites
17 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The study will include 10 women with pure or predominant SUI symptoms, with severe urodynamic stress incontinence on urodynamics defined as loss of urine with sudden increases in abdominal pressure: eg, coughing, sneezing, or laughing). This will be conducted at the Department of Obstetrics and Gynecology, Faculty of Medicine, Al-Azhar University. The purpose of study is to evaluate the efficacy and safety of platelets rich plasma combined with PDO threads in the treatment of stress incontinence in Egyptian women.
CONDITIONS
Official Title
PRP & PDO Threads in Treatment of Stress Incontinence
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Nonpregnant women with stress urinary incontinence
- Age between 20 to 45 years
- History of failed conservative treatment for SUI
- Patients on the waiting list for surgical treatment of SUI
You will not qualify if you...
- Taking anti-platelet agents
- Taking NSAIDs
- Platelet dysfunction syndrome
- Critical thrombocytopenia
- Hypofibrinogenaemia
- Sepsis
- Acute or chronic infections
- Chronic liver disease
- On anti-coagulation therapy
- History of malignancy or active malignant pathology
- Pregnancy
- Mental disorders preventing consent
- Genitourinary fistula
- Pelvic organ prolapse stage greater than 2
- Detrusor overactivity on urodynamics
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Department of Obstetrics and Gynecology, Faculty of Medicine, Al-Azhar University.
Cairo, Egypt
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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