To compare outcomes between a standard protocol and a luteal phase estradiol in infertile patients with poor responders
Phase 2
- Conditions
- poor responder patients in ART(Assisted Reproductive Technology).Other ovarian dysfunction
- Registration Number
- IRCT138901311760N4
- Lead Sponsor
- Vice Chancellor for Research and Technology, Babol University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
Infertile patents with poor ovarian response, Oocytes number<5 or age>37, Basal FSH>12 Or canceled the previous cycle. Exclusion criteria: Patients who do not consent to enter the study.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method umber of oocytes. Timepoint: puncher day. Method of measurement: Counted by the laboratory.;Total fetus. Timepoint: 2 days after puncher. Method of measurement: Counted by the laboratory.
- Secondary Outcome Measures
Name Time Method Pregnancy. Timepoint: 17 days after embryo transfer. Method of measurement: blood BHCG test.