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The SCOPE trial. Study on Cognition and Prognosis in the Elderly
1NHLI Division, Imperial College of Science, Technology and Medicine, Department of Clinical Pharmacology, St Mary's Hospital, London, UK. p.sever@ic.ac.uk
Journal of the Renin-Angiotensin-Aldosterone System : JRAAS
|September 14, 2002
Summary
The SCOPE trial found candesartan did not significantly reduce cardiovascular events or cognitive decline in elderly hypertensive patients. Lowered blood pressure differences limited study power, but subgroup analyses suggested potential benefits.
Area of Science:
- Cardiology
- Geriatrics
- Pharmacology
Background:
- Elderly hypertension management requires outcome data for cardiovascular endpoints and cognitive function.
- Angiotensin receptor blockers are a key therapeutic class for hypertension.
Purpose of the Study:
- To evaluate the efficacy of candesartan versus placebo in reducing cardiovascular events and cognitive decline in elderly hypertensive patients.
Main Methods:
- The Study on Cognition and Prognosis in the Elderly (SCOPE) randomized 4500 elderly hypertensive patients.
- Patients received candesartan or placebo for 4.5 years, monitoring cardiovascular mortality, myocardial infarction, stroke, and cognitive function.
Main Results:
- Candesartan did not significantly reduce the primary endpoint of combined cardiovascular mortality, non-fatal myocardial infarction, and non-fatal stroke (RR 11%, p=0.19).
- No significant difference in cognitive function decline was observed between candesartan and placebo groups.
- Concomitant hydrochlorothiazide use in the placebo group reduced blood pressure differences, potentially impacting study power.
Conclusions:
- Candesartan did not demonstrate a significant benefit in reducing major cardiovascular events or preserving cognitive function in this elderly hypertensive population.
- Further research and subgroup analyses may be warranted to explore potential benefits of candesartan in specific patient groups.

