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Comparison of using of recombinant Fsh long time with or without hMG in IVf/ICSI cycles

Phase 3
Conditions
Female infertility associated with anovulation.
Female infertility associated with anovulation
Registration Number
IRCT201404065181N13
Lead Sponsor
vhice chancellor of
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
200
Inclusion Criteria

Inclusion Criteria:All patients agreed upon ESHRE Criteria 2011 ,advanced maternal age( >40 years )? previous poor ovarian respond (POR)? abnormal ovarian reserve Test ( AFC=5-7, AMH=0.5-1.1)are enrolled.

Exclusion Criteria

Cigaret user; history of ovarian cyst or surjeri in ovary;primary sensitivity to Cinal Or Gonal-F ; Tumors depended to Sex in reproductive systhem ;Adrenal failure or oncontrlod Thyroid;andometriosis;couple chromosomal difficulties;ovulatory dysfunction ( hypogonadic or hypergonadic infertility , hyperprolactinemia,thyroid disease, neoplastic ovary and adrenal,Kushing syndrome).

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Mature oocyte. Timepoint: time of getting oocyte. Method of measurement: microscopic assay.;Number of fetus. Timepoint: two days after getting of oocytes. Method of measurement: microscopic assay by embryologists.
Secondary Outcome Measures
NameTimeMethod
Days of ovulation induction. Timepoint: Medication at the time of ovulation induction. Method of measurement: Patient records.;Abortion. Timepoint: two weeks after embryo transfer. Method of measurement: transvaginal sonography and blood test.;Pregnancy. Timepoint: two weeks after embryo transfer. Method of measurement: transvaginal sonography and blood test.
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