Oral versus vaginal progestogens in women with recurrent miscarriages
Phase 4
- Conditions
- recurrent miscarriages.Spontaneous abortion
- Registration Number
- IRCT20230117057148N1
- Lead Sponsor
- ady Reading Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 108
Inclusion Criteria
Pregnancy
Aged 16-40 years,
A history of at least three recurrent miscarriages
At or less than 7 weeks of gestational age
Exclusion Criteria
Threatened miscarriage,
Breast carcinoma
Structural uterine abnormality distorting the cavity,
Absence of fetal cardiac activity (missed abortion),
Contraindications to progestron use (e.g. allergy to progesterone)
Inadequate treatment compliance
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pregnancy. Timepoint: 12 weeks of gestation. Method of measurement: ultrasound.
- Secondary Outcome Measures
Name Time Method