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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01542411
Other study ID # 2362
Secondary ID
Status Completed
Phase N/A
First received February 25, 2012
Last updated March 1, 2012
Start date April 2008

Study information

Verified date February 2012
Source Yazd Medical University
Contact n/a
Is FDA regulated No
Health authority Iran: Ethics Committee
Study type Observational

Clinical Trial Summary

This study evaluated the effect of anticoagulant treatment on the live-birth rate in women with a history of at least two continuous unexplained miscarriages or thrombophilia. It also compared two methods of treatment with aspirin and aspirin plus heparin.


Recruitment information / eligibility

Status Completed
Enrollment 520
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 19 Years to 35 Years
Eligibility Inclusion Criteria:

- unexplained recurrent miscarriage,

- women had previous venous or arterial thromboembolism or who were heterozygous or homozygous for mutations for FV Leiden G1691A, prothrombin gene G20210A (FII G20210A), and methyltetrahydrofolate reductase C677T (MTHFR C677T)

Exclusion Criteria:

- abnormal karyotypes of both partners,

- uterine and cervical anatomical disorders on pelvic ultrasonography or hysteroscopy,

- abnormal ovaries and abnormal endocrine tests.

Study Design

Observational Model: Case Control, Time Perspective: Retrospective


Locations

Country Name City State
Iran, Islamic Republic of Research and Clinical Centre for Infertility Yazd

Sponsors (1)

Lead Sponsor Collaborator
Yazd Medical University

Country where clinical trial is conducted

Iran, Islamic Republic of, 

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