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| Sponsored by: |
National Heart, Lung, and Blood Institute (NHLBI) |
|---|---|
| Information provided by: | National Heart, Lung, and Blood Institute (NHLBI) |
| ClinicalTrials.gov Identifier: | NCT00005515 |
Purpose
To assess the interaction between hormone replacement therapy and the prothrombotic mutations, Factor V Leiden and the recently described prothrombin mutation (20210A) on the incidence of venous thromboembolism (VTE) in a population-based case-control study conducted at Group Health Cooperative of Puget Sound (GHC).
| Condition |
|---|
|
Cardiovascular Diseases Venous Thromboembolism Postmenopause |
| Study Type: | Observational |
| Study Design: | Natural History |
| Study Start Date: | September 1998 |
| Estimated Study Completion Date: | August 2003 |
BACKGROUND:
Epidemiologic studies have identified Factor V Leiden as the most common cause of heritable thrombophilia, a prothrombotic mutation associated with a 5 to 7-fold increase in the risk of venous thromboembolism (VTE). In pre-menopausal women, the use of oral contraceptives is associated with a 4-fold increase in VTE risk, and the joint effects of oral contraceptive use and Factor V Leiden carriership increase the VTE risk of by a factor of 35.
Recently, the results of several observational studies and randomized clinical trials suggest that in post-menopausal women, the use of hormone replacement therapy is associated with a 3-fold increase in VTE risk. Whether post-menopausal women with prothrombotic mutations experience a similar 20-fold increase in risk when they take post-menopausal hormones remains unknown.
DESIGN NARRATIVE:
In this case-control study, post-menopausal women with a first episode of objectively confirmed venous thromboembolism, and population-based controls were identified and recruited from the GHC enrollment files. Controls were frequency matched to the cases on age and calendar-year. Data collection included a review of ambulatory medical record and a telephone interview. The GHC computerized pharmacy database was used to assess exposure to hormone replacement therapy. A venous blood specimen was obtained from consenting subjects, processed into aliquots of white cells, plasma, and red cells, and stored at 70 degrees C prior to laboratory analysis. DNA was extracted from white cells, and molecular genotyping assays were conducted to assess carriership of prothrombotic mutations.
Eligibility| Ages Eligible for Study: | 30 Years to 89 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
No eligibility criteria
Contacts and Locations
More Information
| Study ID Numbers: | 5033 |
| Study First Received: | May 25, 2000 |
| Last Updated: | July 20, 2005 |
| ClinicalTrials.gov Identifier: | NCT00005515 History of Changes |
| Health Authority: | United States: Federal Government |
|
Embolism and Thrombosis Embolism Vascular Diseases Venous Thromboembolism |
Hormones Thrombosis Thromboembolism |
|
Embolism and Thrombosis Vascular Diseases Cardiovascular Diseases |
Venous Thromboembolism Thrombosis Thromboembolism |