Alzheimer's Disease Clinical Trial
Official title:
Pilot Trial of Carvedilol in Alzheimer's Disease
This is a 6-month pilot randomized double-blind placebo-controlled trial of carvedilol, with the primary objective being to determine whether carvedilol treatment is associated with improvement in Alzheimer's Disease (AD) as compared to placebo treatment. Secondary objectives are to monitor changes in cerebrospinal fluid amyloid levels and whether this dose will be safe and well-tolerated in AD patients. Clinical assessments will be performed at baseline, 3 months, and 6 months, while cerebrospinal fluid and blood samples will be obtained at baseline and 6 months.
The purpose of the study is to measure decline in episodic memory in participants with early
AD taking carvedilol compared to placebo treatment as evidenced by the Hopkins Verbal
Learning Test (HVLT). cerebrospinal fluid levels of Aβ oligomers in early AD, will be
measured in participants receiving carvedilol treatment when compared to placebo treatment.
Adverse effects will be monitored in participants receiving carvedilol when compared to
placebo.
To assess adverse events, routine chemistry and hematology studies, vital signs, and
electrocardiographic parameters before and after 6 months randomized placebo-controlled
double-blind treatment with carvedilol at a target dose of 25 mg daily, comparing 25 early AD
participants taking carvedilol vs. 25 early AD participants taking placebo.
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