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Estrogen priming effect on antagonist cycles in poor responded patient

Not Applicable
Conditions
Female infertility.
Female infertility associated with anovulation
Registration Number
IRCT201602075942N3
Lead Sponsor
Vice Chancellor for Research and Technology University of medical sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
106
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

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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 Outcome Measures
NameTimeMethod
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.
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