Evaluation of nifedipine administration on embyro transfer success rate, a Randomized Clinical Trial
Phase 1
- Conditions
- Female infertility.Female infertility
- Registration Number
- IRCT20201129049532N1
- Lead Sponsor
- Iran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 98
Inclusion Criteria
Women aged 18-40 with primary or secondary infertility
fresh or frozen embryo transfer
good embryo quality(based on defined criteria)
transfer of 3 embryo of two days age
Exclusion Criteria
Blood pressure less than 100/60mmHg
Body mass index > 38 kg/m2
Abnormal uterine cavity(congenital or acquired)
Nifedipine contraindications(history of severe allergic reaction, porphyria, severe heart failure)
Recurrent implantation failure
History of recurrent abortion
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Clinical Pregnancy. Timepoint: Before intervention and 3 weeks after intervention. Method of measurement: Transvaginal ultrasound and serum Bhcg.
- Secondary Outcome Measures
Name Time Method ive birth, multiple gestation, abortion. Timepoint: 3 weeks after intervention, 9 months after intervention if primaryboutcome occured. Method of measurement: Transvaginal ultrasound, successful delivery.