PRP & PDO Threads in Treatment of Stress Incontinence
Recruiting
N/A
Interventional Study
Stress Incontinence, Female
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 20 – 45
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 10 (estimated)
- Sponsor
- Al-Azhar University · Other
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About This Trial
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 a…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Nonpregnant Women with SUI
* Age between 20 to 45 years
* Patients had a history of failed conservative treatment
* Patients were on the waiting list for surgical treatment of SUI
Exclusion Criteria:
* Under anti-platelet agent treatment
* Under NSAIDs
* Platelet dysfunction…
Contacts
No contact information available.