ACTRN12612000891820
Active, Not Recruiting
Phase 4
Study of Neurocognitive Outcomes, Radiological and retinal effects of Aspirin in Sleep Apnoea to determine the effects of daily low-dose aspirin 100mg versus placebo on cognitive outcomes in the setting of sleep apnoea, in healthy older adults aged 70 and over.
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Sleep Apnoea
- Sponsor
- Monash University
- Enrollment
- 1500
- Status
- Active, Not Recruiting
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Enrolling into the parent ASPREE study.
- •Aged 70 and over
- •Able and willing to provide informed consent
Exclusion Criteria
- •History of a diagnosed cardiovascular event, including AMI and stroke, atrial fibrillation, serious intercurrent illness likely to cause death within 5 years, cognitive impairment or dementia, disability, anaemia, a current or recurrent condition with a high risk of major bleeding, absolute contraindication or allergy to aspirin.
- •Also known history of sleep apnoea and/ or current use of continuous positive airways pressure (CPAP) at night
Outcomes
Primary Outcomes
Not specified
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