Effects of Estrogen on Memory in Post-Menopausal Women and Patients With Alzheimer's Disease
NCT ID: NCT00006399
Last Updated: 2009-01-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
45 participants
INTERVENTIONAL
1999-09-30
2004-03-31
Brief Summary
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Detailed Description
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The primary goal of this study is to test the hypothesis that three months of administration of EST to 1) normal post-menopausal women, and 2) female patients with mild-moderate AD who are concurrently treated with anticholinesterase therapy (donepezil), will positively change or blunt the negative and behavioral effects of drugs that block central cholinergic receptors (both muscarinic and nicotinic). Participants will be blindly placed on EST or placebo for three months each. After each three month period, they will be cognitively assessed after receiving single doses of the cholinergic antagonists scopolamine and mecamylamine. These results will have direct implications for the use of EST in post-menopausal women as well as interactive treatment with cholinergic drugs for AD. Researchers plan to recruit a total of 45 women (30 healthy, and 15 patients with AD).
NOTE: This study is only recruiting participants with Alzheimer's Disease at this time.
Conditions
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Study Design
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TREATMENT
DOUBLE
Interventions
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Donepezil
Estrogen
Progesterone
Eligibility Criteria
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Inclusion Criteria
* Non-smoker
* No use of Hormone Replacement Therapy for at least one year
* No menses for at least one year
* Normal mammogram within the last year
* minimum age is 45 for patients with Alzheimer's disease; 50 for normal volunteers
* Maximum age is 85 for patients with Alzheimer's disease; there is no maximum age for normal volunteers.
Exclusion Criteria
* Women who are smokers.
* Women who have had breast cancer.
45 Years
85 Years
FEMALE
No
Sponsors
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Alzheimer's Association
OTHER
Pfizer
INDUSTRY
Eisai Inc.
INDUSTRY
National Center for Research Resources (NCRR)
NIH
Responsible Party
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University of Vermont College of Medicine
Principal Investigators
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Paul A. Newhouse, M.D.
Role: PRINCIPAL_INVESTIGATOR
Memory Center, Department of Psychiatry, University of Vermont College of Medicine
Locations
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Clinical Neuroscience Research Unit, University of Vermont
Burlington, Vermont, United States
Countries
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References
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Newhouse PA, Potter A, Corwin J, Lenox R. Acute nicotinic blockade produces cognitive impairment in normal humans. Psychopharmacology (Berl). 1992;108(4):480-4. doi: 10.1007/BF02247425.
Newhouse PA, Potter A, Corwin J, Lenox R. Age-related effects of the nicotinic antagonist mecamylamine on cognition and behavior. Neuropsychopharmacology. 1994 Apr;10(2):93-107. doi: 10.1038/npp.1994.11.
Newhouse PA, Potter A, Corwin J, Lenox, R. Effects of nicotinic cholinergic agents on cognitive functioning in Alzheimer's and Parkinson's disease. Drug Development Research 38:278-289, 1996.
Related Links
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University of Vermont, Clinical Neuroscience Research Unit
Other Identifiers
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IA0023
Identifier Type: -
Identifier Source: org_study_id
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