Overview
Memory and Mental Health in Aging
Status:
Completed
Completed
Trial end date:
2007-12-01
2007-12-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
This study will evaluate the effectiveness of donepezil (AriceptĀ®) and cognitive training in improving memory performance in elderly adults.Phase:
N/AAccepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Stanford UniversityCollaborator:
National Institute of Mental Health (NIMH)Treatments:
Donepezil
Criteria
Inclusion Criteria:- Mini-Mental Exam score between 24 and 30
- Hamilton Depression Score of 12 or less on 17-item scale
- Visual and auditory acuity adequate for neuropsychological testing
- General good health (no additional diseases expected to interfere with the study)
- Normal B12, Rapid Plasma Reagin (RPR), and Thyroid Function Tests
- Normal general clinical chemistry, complete blood count, and electrocardiogram (ECG)
- Female participants must be 2 years postmenopausal or surgically sterile
Exclusion Criteria:
- Significant neurologic disease
- Possible or probable Alzheimer's Disease (AD)
- Parkinson's disease
- Multi-infarct dementia
- Huntington's disease
- Normal pressure hydrocephalus
- Brain tumor
- Progressive supranuclear palsy
- Seizure disorder
- Subdural hematoma
- Multiple sclerosis
- History of significant head trauma followed by persistent neurologic defaults or known
structural brain abnormalities
- Major depression or other major psychiatric disorder as described in DSM IV within the
past 2 years
- Psychotic features, agitation, or behavioral problems within the last 3 months
- History of alcohol or substance abuse or dependence within the past 2 years
- Significant systemic illness or unstable medical condition including: a) history of
systemic cancer within the last 5 years (nonmetastatic skin cancers are acceptable);
b) history of myocardial infarction within the past year or unstable or severe
cardiovascular disease, including angina or CHF with symptoms at rest; c) clinically
significant obstructive pulmonary disease or asthma; d) clinically significant and
unstable gastrointestinal disorder such as ulcer disease or a history of active or
occult gastrointestinal bleeding within 2 years; e) clinically significant laboratory
test abnormalities on the battery of screening tests (hematology, prothrombin time,
chemistry, urinalysis, ECG); f) insulin-requiring diabetes or uncontrolled diabetes
mellitus; g) uncontrolled hypertension (systolic BP greater than 170 or diastolic
greater than 100); h) history of clinically significant liver disease, coagulopathy,
or vitamin K deficiency within the past 2 years
- Use of centrally active beta-blockers, narcotics, methyldopa, and clonidine within 4
weeks prior to screening
- Use of anti-Parkinsonian medications (e.g. Sinemet, amantadine, bromocriptine,
pergolide, and selegiline) within 2 months prior to screening
- Use of neuroleptics or narcotic analgesics within 4 weeks prior to screening
- Use of long-acting benzodiazepines or barbiturates within 4 weeks prior to screening
- Use of short-acting anxiolytics or sedative hypnotics more frequently than 2 times per
week within 4 weeks prior to screening (note: sedative agents should not be used
within 72 hours of screening)
- Initiation or change in dose of an antidepressant lacking significant cholinergic side
effects within the 4 weeks prior to screening (use of stable doses of antidepressants
for at least 4 weeks prior to screening is acceptable)
- Use of systemic corticosteroids within 3 months prior to screening
- Medications with significant cholinergic or anticholinergic side effects (e.g.
pyridostigmine, tricyclic antidepressants, meclizine, and oxybutynin) within 4 weeks
prior to screening
- Use of anti-convulsants (e.g. Phenytoin, Phenobarbital, Carbamazepine) within 2 months
prior to screening
- Use of warfarin (Coumadin) within 4 weeks prior to screening
- Prior use of any FDA approved medications for the treatment of AD (e.g. tacrine,
donepezil, or other newly approved medications)