Autologous platelet-rich plasma in women with Asherman's syndrome
Phase 3
Recruiting
- Conditions
- Asherman Syndrome.Intrauterine synechiae
- Registration Number
- IRCT20110509006420N17
- Lead Sponsor
- Yazd University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 30
Inclusion Criteria
All patients with Asherman's syndrome who have been diagnosed with ultrasound, sonography, hysterography or hysteroscopy.
Exclusion Criteria
Severe cervical stenosis
Coagulation disorders
Mullerian anomaly
systemic disorders
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Adhesion scoring. Timepoint: 4 to 6 weeks after hysteroscopy. Method of measurement: With hysteroscopy & ASRM score.
- Secondary Outcome Measures
Name Time Method