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Efficiency of low dose aspirin for prevention of complications for in vitro fertilization cycles of the patient with polycystic ovarian syndrome

Phase 2
Completed
Conditions
polycystic ovarian syndrome.
Polycystic ovarian syndrome
Registration Number
IRCT201105216541N1
Lead Sponsor
Infertility research center, Shiraz university of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
80
Inclusion Criteria

polycystic ovarian syndrome (PCOS) confirmed by: Hyperandrogenism (clinical and/or biochemical); Ovarian dysfunction (oligo-anovulation and/or polycystic ovaries); The exclusion of other androgen excess or related disorders.
Exclusion criteria: All of the patients with Known hypersensitivity to ASA or previous gastritis or GI bleeding.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
umber of follicles. Timepoint: every 3-4 days. Method of measurement: by Ultra sound scan.;Serum Estradiol. Timepoint: every 3-4 days. Method of measurement: serum level of Estradiol.
Secondary Outcome Measures
NameTimeMethod
Ovarian size more than 5 cm. Timepoint: 3-4 days. Method of measurement: ultra sound.;Ovarian size more than12 cm. Timepoint: 3-4 days. Method of measurement: ultra sound.
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