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Comparison of double stimulation protocol with high dose of gonadotropin protocol in patients with poor ovarian response

Comparison of double stimulation protocol to the approach using antagonist with high dose of gonadotropin in patients with poor ovarian response in avicenna infertility center

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180219038792N1
Enrollment
60
Registered
2019-01-02
Start date
2018-04-04
Completion date
Unknown
Last updated
2019-01-29

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

Conditions

Poor ovarian responds patients. Ovarian dysfunction

Interventions

Intervention 1: This study is a prospective randomized clinical trial. Patients who are nominated for ICSI because of POR are divided into two groups of 30 individuals randomly. After completing the c

Sponsors

Iranian academic center for education culture and research
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
40 Years to 45 Years

Inclusion criteria

Inclusion criteria: Age over 40. History of getting less than four oocyte retival in previous cycle Abnormal ovarian reserve tests. History of previous ovarian surgery or history of chemotherapy Different risk factors involved in ovarian response weakness

Exclusion criteria

Exclusion criteria: BMI value is equal to 35 and higher FSH more than 25 Grade 3 endometriosis and higher Any contraindication for ovarian stimulation such as uncontrolled systemic diseases Sever male infertility based on WHO indexes

Design outcomes

Primary

MeasureTime frame
1-The number of retrieved oocytes. Timepoint: Measuring the number of follicles in the first menstrual cycle and after taking ovulation-inducing drugs. Method of measurement: Ultrasouand system.;The number and quality of the obtained embryos. Timepoint: In follicular and luteal phase. Method of measurement: Ultrasouand system.;Measurement of serum Progesterone. Timepoint: On the day the gonadotropins started, and on the day of the trigger with Deca in the follicular and luteal phase. Method of measurement: ELISA.;Measurement of serum E2,. Timepoint: On the day the gonadotropins started, and on the day of the trigger with Deca in the follicular and luteal phase. Method of measurement: ELISA.;Measurement of serum LH. Timepoint: On the day the gonadotropins started, and on the day of the trigger with Deca in the follicular and luteal phase. Method of measurement: ELISA.;Measurement of serum FSH. Timepoint: On the day the gonadotropins started, and on the day of the trigger with Deca in the follicular and luteal phase. Method of measurement: ELISA.;The quantity of retrieved oocytes. Timepoint: Measuring in the first menstrual cycle and after taking ovulation-inducing drugs. Method of measurement: Ultrasouand system.

Secondary

MeasureTime frame
The amount of pregnancy and successful birth. Timepoint: After 9 months. Method of measurement: Number of successful pregnancies and live births.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarnaz Montazeri

Iranian academic center for education culture and research

f.montazeri@ari.ir+98 21 23519

Outcome results

None listed

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