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Comparison of the oocyte quality in patients with poor ovarian response undergone two triggering methods.

Phase 3
Conditions
Infertility.
Complication associated with artificial fertilization, unspecified
N98.9
Registration Number
IRCT20190409043207N2
Lead Sponsor
Yazd University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
122
Inclusion Criteria

Age more than 40 years or other risk factors for poor ovarian response.
Less than three oocytes in the previous IVF cycle
Abnormal ovarian reserve test
Two histories of poor ovarian response following receiving maximal stimulation

Exclusion Criteria

Severe male factor
Untreated endocrine disorders
Severe uterine anomaly

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Clinical pregnancy rate. Timepoint: Four weeks after positive beta hCG. Method of measurement: Fetal heart activity by trans-vaginal ultrasonography.
Secondary Outcome Measures
NameTimeMethod
Biochemical pregnancy rate. Timepoint: 14 days after embryo transfer. Method of measurement: Positive B-HCG.;Implantation rate. Timepoint: 4 weeks after embryo transfer. Method of measurement: It is defined as the numbers of gestational sacs that detected throughout sonography per number of embryos transferred (100 embryo).;Abortion rate. Timepoint: Before 20th weeks of gestation. Method of measurement: Observation and counting.;COC counting. Timepoint: The day of oocyte puncture. Method of measurement: Counting.;MII oocyte number. Timepoint: The day of puncture. Method of measurement: Counting.;2PN number. Timepoint: 1 day after fertilization. Method of measurement: Counting.;Estradiol level. Timepoint: In the day of hCG injection. Method of measurement: Biochemical measurements in the blood.;Embryo grading. Timepoint: 3 days after puncture. Method of measurement: Observation and grading according to the embryo references.
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