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Comparison of controlled ovarian stimulation with clomiphen citrate HMG(Human menopausal gonadotropin) or clomiphen citrate rFSH(recombinant follicule stimulating hormon) in IUI(Intrauterine Insemination) cycles.

Comparison of controlled ovarian stimulation with clomiphen citrate HMG(Human menopausal gonadotropin) or clomiphen citrate rFSH(recombinant follicule stimulating hormon) in IUI(Intrauterine Insemination)cycles.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201109163386N4
Enrollment
142
Registered
2011-10-01
Start date
2009-06-18
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

Condition 1: Unexplained infertility. Condition 2: Male factor infertility. Female infertility, unspecified Oligospermia NOS

Interventions

Intervention 1: Ovarian cycle stimulation was started on the 3rd day of menstruation after the basal transvaginal ultrasound (TV-USG) with 100 mg CC for 5 consecutive days.The gonadotropin regimens ad
Treatment - Drugs
Ovarian cycle stimulation was started on the 3rd day of menstruation after the basal transvaginal ultrasound (TV-USG) with 100 mg CC for 5 consecutive days.The gonadotropin regimens adopted in each gr
Ovarian cycle stimulation was started on the 3rd day of menstruation after the basal transvaginal ultrasound (TV-USG) with 100 mg CC for 5 consecutive days.The gonadotropin regimens adopted was rFSH 7

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: history of infertility of more than 1 year; wemon's age between 20 and 40 years old; documentation of normal ovulatory cycles; normal TSH and Prolactin level; normal reproductive hormones in the early follicular phase;patent tubes have been shown by HSG or laparoscopy; normal sperm count, motility and morphology according to the World Health Organization criteria(WHO 1992)in unexplained infertility and total motile sperm count more than 1 million in male factor infertility.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Clinical pregnancy rate. Timepoint: 7 weeks of gestation. Method of measurement: Fetal heart activity with ultrasound.;Ongoing pregnancy rate. Timepoint: 12 weeks of gestation. Method of measurement: Fetal heart activity with ultrasound.

Secondary

MeasureTime frame
Mean of follicular size on the day of HCG administration. Timepoint: Day of occurrence of at least one ovarian follicule =16 mm in diameter. Method of measurement: Ultrasound.;Endometrial thickness on the day of HCG administration. Timepoint: Day of occurrence of at least one ovarian follicule =16 mm in diameter. Method of measurement: Ultrasound.;Total dose of gonadotropin. Timepoint: Day of occurrence of at least one ovarian follicule =16 mm in diameter. Method of measurement: Number of vials.;Duration of stimulation with gonadotropin. Timepoint: Day of occurrence of at least one ovarian follicule =16 mm in diameter. Method of measurement: Number of days gonadotropin was administered.;Number of dominant follicles on the day of HCG administration. Timepoint: Day of occurrence of at least one ovarian follicule =16 mm in diameter. Method of measurement: Number of dominant follicles.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarjan Bahrami

Semnan University of Medical Sciences

bahrami.marjan@yahoo.com+98 23 1446 0088

Outcome results

None listed

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