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Comparing two different drug methods for infertility treatment by assisted reproduction techniques (ARTs)

Investigation of outcome of assessment reproduction treatment and prevention of ovarian hyper stimulation syndrome in GnRH agonist protocol compared to GnRH antagonist protocol

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201205309910N1
Enrollment
136
Registered
2012-06-24
Start date
2011-01-22
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

infertility. Female infertility

Interventions

Intervention 1: Group A: a daily dose of Buserelin 500 µg given SC and commenced 21th day of cycle, and vaginal ultrasonography continued onward until estradiol on the 2nd day of cycle. Intervention 2
Treatment - Drugs
Group A: a daily dose of Buserelin 500 µg given SC and commenced 21th day of cycle, and vaginal ultrasonography continued onward until estradiol on the 2nd day of cycle.
Group B: GnRH antagonist was administered. Ovarian stimulation was started on the 2nd day of the cycle by SC injection of 75 IU of FSH daily. On the 6th day of stimulation, 0.25 mg Cetrorelix was init

Sponsors

Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
No minimum to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: undergoing assisted reproduction techniques (ARTs) for the first time, age =35years and serum FSH level =10 IU/liter. Exclusion criteria: women with the previous history of IVF or ICSI; patients who had hyperprolactinemia, thyroid dysfunction, uterine abnormality, severe endometriosis and secondary infertility.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Ovarian hyperstimulation syndrome. Timepoint: 10 days after HCG injection and during primary Trimester. Method of measurement: as presence of enlarged ovarian cysts more than 12 by 12 cm, ascites, pleural and/or pericardial effusion, electrolyte imbalance ,hypovolemia, and hypovolemic shock.;Fertility. Timepoint: after primary Trimester. Method of measurement: ultrasonography.

Secondary

MeasureTime frame
Number of retrieved oocytes. Timepoint: 2 weeks after intervention. Method of measurement: number of retrieved oocytes in retrieval day.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSetare Nasiri Zeydi

Isfahan University of Medical Sciences

setare_n99@yahoo.com+98 911 255 6829

Outcome results

None listed

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