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Estrogen priming effect on antagonist cycles in poor responded patient

Estrogen priming effect on antagonist cycles in poor responded patient

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201602075942N3
Enrollment
106
Registered
2016-04-26
Start date
2016-04-16
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. Female infertility associated with anovulation

Interventions

Intervention 1: Intervention group: From 21 days of cycle before the IVF , will be start oral estradiol valerate with 2 mg daily and will continue to the next cycle until the second day of the next c
Treatment - Drugs
Intervention group: From 21 days of cycle before the IVF , will be start oral estradiol valerate with 2 mg daily and will continue to the next cycle until the second day of the next cycle. ovarian s
Control group: The control group also entered the antagonist and the gonadotropin treatment cycle , without treatment with estradiol.

Sponsors

Vice Chancellor for Research and Technology University of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
19 Years to 42 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Women 19 to 42 years old with low ovarian reserve; Women who have not responded to treatment with short antagonist protocol and gonadotropin or the number of oocytes has been equal to or less than 3. Exclusion criteria: who do not respond to treatment or have a cycle of follicle has been canceled; People who have certain diseases like hypothyroidism or hyper prolactin; If patients have complications such as embolism and contraindications to estrogen

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The number of mature follicles. Timepoint: 14 day of menstrual cycle. Method of measurement: Ultrasound.;Oocytes and embryos obtained count. Timepoint: 14 day of menstrual cycle. Method of measurement: Ultrasound.

Secondary

MeasureTime frame
Chemical and clinical pregnancy rate. Timepoint: After the delay period. Method of measurement: Tests and ultrasound.;The resulting embryo count. Timepoint: A month after a positive pregnancy test. Method of measurement: Ultrasound.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Aliyeh Ghasemzadeh

Tabriz University of medical Sciences

lahroudin@gmail.com00

Outcome results

None listed

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