Journal article
Study design of ASPirin in Reducing Events in the Elderly (ASPREE): A randomized, controlled trial
R Grimm, JJ McNeil, W Applegate, L Beilin, S Espinoza, CI Johnston, B Kirpach, K Margolis, A Murray, MR Nelson, CM Reid, R Shah, E Storey, AM Tonkin, P Wilson, R Wolfe, RL Woods, W Abhayaratna, D Ames, L Cobiac Show all
Contemporary Clinical Trials | ELSEVIER SCIENCE INC | Published : 2013
Abstract
Cost-effective strategies to maintain healthy active lifestyle in aging populations are required to address the global burden of age-related diseases. ASPREE will examine whether the potential primary prevention benefits of low dose aspirin outweigh the risks in older healthy individuals. Our primary hypothesis is that daily oral 100. mg enteric-coated aspirin will extend a composite primary endpoint termed 'disability-free life' including onset of dementia, total mortality, or persistent disability in at least one of the Katz Activities of Daily Living in 19,000 healthy participants aged 65. years and above ('US minorities') and 70. years and above (non-'US minorities'). ASPREE is a double-..
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Awarded by National Institute on Aging
Funding Acknowledgements
ASPREE is registered on the International Standard Randomized Controlled Trial Number Register (ISRCTN83772183). ASPREE has received project grants from the National Institute on Aging, the National Health and Medical Research Council (Australia), Heart Foundation (Australia), the National Cancer Institute and the Victorian Cancer Agency (Australia). Bayer Pharma AG provides blinded aspirin and placebo. ASPREE has multiple IRB approvals in the US and Australia.