Aspirin Responsiveness in Women at Risk for Cardiac Events

Status Completed

Clinical Trial Summary

The objective of this pilot study is to evaluate the prevalence of biological aspirin resistance in women at risk for CHD taking low dose (81 mg) aspirin. Aspirin responsiveness will be measured with the VerifyNow device (Accumetrics; San Diego, CA). Those women identified as biologically resistant will be switched to aspirin 325 mg for 14 days and then re-tested for aspirin responsiveness.

Clinical Trial Description

n/a

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Heart Disease

Clinical Trial Details

NCT number	NCT00818337
Study type	Interventional
Source	Creighton University
Contact
Status	Completed
Phase	Phase 4
Start date	November 2008
Completion date	June 2009

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