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Completed NCT04522739

Spironolactone Safety in African Americans With Mild Cognitive Impairment and Early Dementia

Conditions: Mild Cognitive Impairment, Alzheimer Disease

Sex: All
Ages: 50 Years – N/A
Healthy volunteers: No
Phase: PHASE4
Enrollment: 25
Sponsor: Emory University

Location: Emory Clinic at Executive Park Atlanta Georgia

Summary

The purpose of this study is to investigate whether a blood pressure medication, spironolactone, can be tolerated by older African American adults that have memory and thinking problems, also called mild cognitive impairment (MCI). This study will also investigate the effect of spironolactone on memory and thinking abilities as measured by performance on cognitive tests, which are tests that measure memory and thinking skills. Participants will take spironolactone or a placebo for one year and will have 4 to 5 study visits during the study period.

Eligibility Criteria

Inclusion Criteria: * Signed and dated informed consent form * Willingness to comply with all study procedures and availability for the duration of the study * Self-identified African American * Blood pressure (BP) and hypertension criteria: normotensive and hypertensive participants will be eligible * Normotensive criteria: BP 110-140/40-90 mmHg and not receiving any treatment for hypertension * Hypertensive criteria: only controlled hypertensives will be eligible with BP range as in the normotensive criteria of 110-140/40-90 mmHg * MCI defined as: * Abnormal memory function per the Logical Memory subscale (Delayed Paragraph Recall, Paragraph A only) from the Wechsler Memory Scale-Revised (the maximum score is 25): * Score \

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT04522739). StuddyBuddy aggregates publicly available trial information.