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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01176305
Other study ID # RAV1
Secondary ID
Status Completed
Phase N/A
First received August 5, 2010
Last updated August 5, 2010

Study information

Verified date October 2009
Source Hillerod Hospital, Denmark
Contact n/a
Is FDA regulated No
Health authority Denmark: The Regional Committee on Biomedical Research Ethics
Study type Observational

Clinical Trial Summary

The purpose of this study is to describe the incidence of thromboembolic events in relation to pregnancy and when in pregnancy and the puerperal period.


Description:

Venous thromboembolism (VTE) still causes maternal death in the western world. The purpose of this study is to estimate the relative and absolute risk of VTE at different gestational ages in pregnant women compared to non-pregnant women.

All Danish Women 15 to 49 years old in the period January 1995 through December 2005, free of previous VTE and current use of oral contraceptives are included.Non-pregnant women are controls.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 15 Years to 50 Years
Eligibility Inclusion Criteria:

- Danish woman at 15 to 49 years old in the period January 1995 through December 2005.

- Free of previous VTE and current use of oral contraceptives.

Exclusion Criteria:

- Previous VTE or current use of oral contraceptives.

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Hillerod Hospital, Denmark

Outcome

Type Measure Description Time frame Safety issue
Primary Absolute incidence of thromboembolic event
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