Guanfacine Treatment for Prefrontal Cognitive Dysfunction in Elderly Subjects
Completed · Not applicable · Has a placebo group
Conditions studied: Cognitive Aging
In brief
This proposal aims to determine whether low does of the alpha-2A-adrenoceptor agonist guanfacine can improve deficits in prefrontally-mediated cognitive functions in healthy elderly subjects.
Key facts
- Study ID
- NCT00935493
- Run by
- Yale University
- People needed
- 154
- Starts
- 2009-06-01
- Expected to finish
- 2012-08-01
- Last updated by the study team
- 2014-08-13
Who can join
Age: 75 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Subjects enrolled will be nondemented, male and female individuals who meet the following inclusion criteria:
- 75 years of age or older
- Fluent in English
- Stable medical condition for at least 4 weeks prior to Screening visit
- Stable dose of non-excluded medications for at least 4 weeks prior to Screening visit
You may not qualify if…
- Dementia
- Mild Cognitive Impairment (Amnestic MCI)
- Clinically significant neurologic disease
- Clinically significant or unstable medical conditions that would interfere with participation in the trial
- Known hypersensitivity to guanfacine
- History of alcohol or substance abuse or dependence within the past 5 years
- Active major psychiatric disorders, including major depression
- History of mental retardation
- Significant abnormalities on clinical laboratories, ECG, or physical examination
- Impairment of visual or auditory acuity sufficient to interfere with completion of study procedures
- Education level < 6 years
Where it is running
- Alzheimer's Disease Research Unit, Yale University School of Medicine — New Haven, Connecticut, United States
Full record on ClinicalTrials.gov
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