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Aspirin and heparin in recurrent pregnancy loss treatment

Not Applicable
Conditions
recurrent pregnancy loss.
Spontaneous abortion
Registration Number
IRCT2013102315123N1
Lead Sponsor
Research and Clinical Center for Infertility,Yazd, Iran
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
252
Inclusion Criteria

unexplained recurrent pregnancy loss; women with thrombophilia exclusion criteria: abnormal karyotypes of each partner; uterine; cervical anatomical disorders on pelvic ultrasonography; hysteroscopy; abnormal ovaries function; abnormal endocrine tests; and antiphospholipid syndrome

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pregnancy after 20 weeks. Timepoint: after 20 weeks. Method of measurement: Sonography.
Secondary Outcome Measures
NameTimeMethod
ive-birth rates. Timepoint: 2 weeks after intervention. Method of measurement: mesearment of blood beta hCG.
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