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Efficacy of Myo-inositol on microinjectio

Phase 1
Conditions
Female infertility.
Female infertility
Registration Number
IRCT20180417039338N1
Lead Sponsor
Babol University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Female
Target Recruitment
90
Inclusion Criteria

Women aged 20-40 years
with Polycystic ovary syndrome
with oligomenorrhea cycles
FSH levels <10
no hormonal treatment during the last 6 months

Exclusion Criteria

with endometriosis
History of oophorectomy
Age over 40 and under 20 years
women with infertility due to male factor
BMI <17 or BMI> 30
Endocrine diseases such as hyperprolactinemia, thyroid dysfunction, adrenal insufficiency and Cushing's disease

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
umber of Oocytes. Timepoint: On the oocyte collection day. Method of measurement: Using ovulation test kits.;Oocyte quality. Timepoint: On the oocyte collection day. Method of measurement: Morphologic assesment with microscope.
Secondary Outcome Measures
NameTimeMethod
umber of embryos. Timepoint: 2 or 3 days after oocyte collection. Method of measurement: Morphologic assesment with microscope.;Embryo quality. Timepoint: 2 or 3 days after oocyte collection. Method of measurement: Morphologic assesment with microscope.;Fertilization rate. Timepoint: 2 or 3 days after oocyte collection. Method of measurement: (embros number/injected oocytes numbers) * 100.
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