Effect of using extract of foeniculum vulgare with induction ovulation versus induction ovulation alone on pregnancy outcomes through invitro fertilization in infertile women with poor ovarian response
Phase 2
- Conditions
- infertility.Female infertility
- Registration Number
- IRCT201411269014N48
- Lead Sponsor
- Vice-chancellor for Research the Technology, Hamadan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 15
Inclusion Criteria
(a) infertility with poor ovarian response; (b) age of 35 years; (c) FHS equal to or greater than 10 mIU/ml on the third day of menstrual period; (d) ovarian volume equal to or greater than 3 ml; (e) history of unsuccessful IVF; (f) number of ovules less than 3 to 5.
Exclusion criteria: (a) FSH more than 20 mIU/ml on the second to fourth days of menstrual period; (b) women with uterine anomaly or obstruction of uterine tube; (c) using corticosteroid during the last 5 months; (d) contraindication of pregnancy; (e) missing of one ovary; (f) systemic diseases such as diabetes, adrenal dysfunction, hypothalamus tumor, hyperprolactinemia, and intracranial damages.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method umber of follicles. Timepoint: before and 2 months after intervention. Method of measurement: using ultrasonography.;Number of ovule. Timepoint: before and 2 months after intervention. Method of measurement: using microscope.;Number of fetus. Timepoint: before and 2 months after intervention. Method of measurement: using microscope.;Number of pregnancy. Timepoint: before and 2 months after intervention. Method of measurement: using ultrasonography.
- Secondary Outcome Measures
Name Time Method umber of receiving HMG. Timepoint: before and 2 months after intervention. Method of measurement: through checking medical record.;Number of induction. Timepoint: before and 2 months after intervention. Method of measurement: through checking medical record.