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

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

45 participants

Study Classification

INTERVENTIONAL

Study Start Date

1999-09-30

Study Completion Date

2004-03-31

Brief Summary

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The goal of this study is to examine whether the administration of estrogen to post-menopausal women and women with mild to moderate Alzheimer's disease will enhance their memory and their capacity for learning.

Detailed Description

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Estrogen (EST) may have significant benefits in preserving cognitive functioning in normal aging after menopause and in decreasing the incidence of Alzheimer's disease (AD). On a molecular level, EST has effects on a variety of cholinergic neuronal and receptor-mediated mechanisms that may be responsible for these beneficial effects. These neurons have critical relevance for the development of age-related cognitive changes and dementing disorders. However, little is known about the clinical relevance of EST-cholinergic interactions, either in normal aging or in AD.

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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Alzheimer Disease

Study Design

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Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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Donepezil

Intervention Type DRUG

Estrogen

Intervention Type DRUG

Progesterone

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Normal volunteers and women with mild Alzheimer's disease:
* 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 currently taking estrogen therapy.
* Women who are smokers.
* Women who have had breast cancer.
Minimum Eligible Age

45 Years

Maximum Eligible Age

85 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Alzheimer's Association

OTHER

Sponsor Role collaborator

Pfizer

INDUSTRY

Sponsor Role collaborator

Eisai Inc.

INDUSTRY

Sponsor Role collaborator

National Center for Research Resources (NCRR)

NIH

Sponsor Role lead

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

Site Status

Countries

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United States

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.

Reference Type BACKGROUND
PMID: 1410163 (View on PubMed)

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.

Reference Type BACKGROUND
PMID: 8024677 (View on PubMed)

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.

Reference Type BACKGROUND

Related Links

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http://www.uvm.edu/~cnru/

University of Vermont, Clinical Neuroscience Research Unit

Other Identifiers

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2R56AG021476

Identifier Type: NIH

Identifier Source: secondary_id

View Link

IA0023

Identifier Type: -

Identifier Source: org_study_id

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