Status:
TERMINATED
MemoryXL Effects on Mild Cognitive Impairment Patients
Lead Sponsor:
University of Oklahoma
Conditions:
Mild Cognitive Impairment
Eligibility:
All Genders
55-85 years
Phase:
PHASE2
Brief Summary
A vitamin nutriceutical, Memory XL, has been shown to provide maintenance of cognitive status in mild, moderate, and severe Alzheimer's disease patients (2 publications by T. Shea). Because this nutri...
Detailed Description
This IRB-approved study is a randomized double blind study of patients diagnosed with Mild Cognitive Impairment (MCI) in the Center for Alzheimer's and Neurodegenerative Disorders (CANDO) at VAMC in O...
Eligibility Criteria
Inclusion
- MCI patients diagnosed at the VAMC Center for Alzheimers and Neurodegenerative Disorder (CANDO).
- Clinical Dementia Rating (CDR) score of 0.5.
- fluent in English.
- able to ambulate to the outpatient clinic and research laboratory
- have sight and hearing levels sufficient to complete neuropsychological testing.
- free from bipolar disorder and terminal illnesses such as cancer.
- must live with a spouse or adult relative who will record nutriceutical ingestion daily.
- subjects will be consecutively diagnosed patients from all ethnic groups.
Exclusion
- patients from protected categories such as prisoners and pregnant women.
- any MCI subject who develops a life-threatening disease such as terminal cancer, stroke, brain trauma, debilitating heart attack, etc.
- indication of inability to make decisions regarding study participation.
Key Trial Info
Start Date :
June 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2011
Estimated Enrollment :
10 Patients enrolled
Trial Details
Trial ID
NCT00903695
Start Date
June 1 2009
End Date
May 1 2011
Last Update
January 26 2012
Active Locations (2)
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1
Univ. of Okla. Health Sciences Center & VAMC OKC
Oklahoma City, Oklahoma, United States, 73104
2
Veterans Affairs Medical Center
Oklahoma City, Oklahoma, United States, 73104