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| Sponsored by: |
Department of Veterans Affairs |
| Information provided by: | Department of Veterans Affairs |
| ClinicalTrials.gov Identifier: | NCT00018278 |
Purpose
The main purpose of this study is to determine the electrophysiological effects of cholinergic therapy (cholinesterase inhibitors and transdermal nicotine) in Alzheimer disease. The attempt will be to locate electrophysiological markers and predictors of cognitive and clinical treatment response.
| Condition | Intervention | Phase |
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Alzheimer Disease |
Drug: Aricept Drug: Exelon Drug: Nicoderm Patch |
Phase IV |
| Genetics Home Reference related topics: | Alzheimer disease |
| MedlinePlus related topics: | Alzheimer's Disease |
| Drug Information available for: | Donepezil E 2020 Rivastigmine SDZ-ENA 713 Nicotine polacrilex Nicotine tartrate |
| Study Type: | Interventional |
| Study Design: | Treatment, Non-Randomized, Open Label, Uncontrolled, Crossover Assignment, Efficacy Study |
| Official Title: | Verbal Memory ERPs as Indices of Treatment Response in Alzheimer Disease |
Eligibility
| Ages Eligible for Study: | 55 Years to 85 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Patients diagnosed with mild to moderate probable Alzheimer's disease (mini-mental state exam scores between 15-27), and normal controls (age generally between 60-85). Subjects must either be planning to start daily cholinesterase therapy (e.g. Aricept, Exelon) or willing to try a transdermal nicotine patch for two 8 hour periods.
Contacts and Locations| United States, California | |||||
| Department of Veterans Affairs | |||||
| San Diego, California, United States, 92161 | |||||
| Investigator: | Vincente Iragui, M.D., Ph.D | |
| Investigator: | Shuanna Morris, Ph.D. |
More Information
| Study ID Numbers: | AGCG-004-98S |
| First Received: | July 3, 2001 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00018278 |
| Health Authority: | United States: Federal Government |
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