PRP & PDO Threads in Treatment of Stress Incontinence
ConditionStress Incontinence, Female
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age20-45
SponsorAl-Azhar University
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 and safety of platelets rich plasma combined with PDO threads in the treatment of stress incontinence in Egyptian women.
Eligibility criteria
Qualifiers
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
Disqualifiers
Under anti-platelet agent treatment
Under NSAIDs
Platelet dysfunction syndrome
Critical thrombocytopenia
Trial design
Treatments tested in this trial
- platelets rich plasma combined with PDO threads
Treatment groups
10 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov