Efficacy of low-dose hCG adjunct to r-hFSH plus GnRH antagonist for ovarian stimulation in assisted reproductive technology
Phase 2
- Conditions
- infertility.Female infertility associated with anovulation
- Registration Number
- IRCT201211197165N2
- Lead Sponsor
- Vice Chancellor for Research, Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 120
Inclusion Criteria
infertile female patient; age between 20-39 years old; body mass index(BMI) of 20- 25 kg/m2; a normal uterus and two functional ovaries; day 3 FSH level< 10 IU/L and E2 level< 60 pg/ml.Exclusion criteria: history of > 2 unsuccessful IVF/ICSI attempts; poor ovarian response in previous IVF/ICSI treatment and any endocrine disorders.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Beta-hCG level. Timepoint: 15 days after oocyte retrieval. Method of measurement: By laboratory kit from blood sample.
- Secondary Outcome Measures
Name Time Method umber of mature oocytes. Timepoint: 35-36 hours after high-dose hCG injection. Method of measurement: Transabdominal ultrasound.