Estrogen Use in Protection From Cognitive Decline
Completed
Conditions studied: Aging, Menopause
In brief
This study is designed to assess the effects of estrogen therapy among postmenopausal women at risk for cognitive decline.
Key facts
- Study ID
- NCT00097058
- Run by
- Stanford University
- People needed
- 71
- Starts
- 2003-08-01
- Expected to finish
- 2014-11-01
- Last updated by the study team
- 2014-11-19
Who can join
Age: 45 and older, up to 65. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Women between the ages of 45 and 65
- Currently on hormone replacement
- One year or more post complete cessation of menses
- Willing to sign the Human Subject Protection Consent form prior to enrollment in the study
- Willing to be randomized to continue or discontinue estrogen therapy
- Adequately visually and auditorially acute to allow neuropsychological testing
- Beyond 8 years of educational achievement to allow adequate neuropsychological testing
- Willing to undergo brain imaging
- At risk for cognitive decline, as defined by one or more of the following: Personal or family history of mood disorder, Hypothyroidism, Diabetes, Family history of Alzheimer's, APOE-4 allele
You may not qualify if…
- Diagnosis of possible or probable Alzheimer's disease or dementia
- Cerebrovascular disease or uncontrolled hypertension (systolic BP >170 or diastolic BP >100)
- History of myocardial infarction within previous year or unstable heart disease
- History of significant liver disease, pulmonary disease, or current cancer
- Contraindication for MRI (metal in body, claustrophobia, etc.)
Where it is running
- Stanford University School of Medicine, Dept. of Psychiatry and Behavioral Sciences — Stanford, California, United States
Full record on ClinicalTrials.gov
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