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

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

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201404065181N13
Enrollment
200
Registered
2014-06-02
Start date
2014-12-20
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Female infertility associated with anovulation. Female infertility associated with anovulation

Interventions

Intervention 1: Control group: A dose of 150 mcg corrifolitropin alfa received on the third day of the menstrual cycle , Antagonist drug Orgalutran, 5 mg is given on the seventh day. Then, during th
Treatment - Drugs
Control group: A dose of 150 mcg corrifolitropin alfa received on the third day of the menstrual cycle , Antagonist drug Orgalutran, 5 mg is given on the seventh day. Then, during the monitoring cy
Intervention group: A dose of 150 mcg corrifolitropin alfa is administrated on the third day of the menstrual cycle. Antagonist drug Orgalutran, 5 mg is given on the seventh day. Then on the sevent

Sponsors

vhice chancellor of
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

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).

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr,Batoolashidi

Vali-e-Asr reproductive HealthnResearch center

bhrashidi@yahoo.com+98 21 6658 1616

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026