Electrophysiologic Measures of Treatment Response in Alzheimer Disease

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...

Date First Received: July 3, 2001

Last Updated: January 20, 2009

Verified by: Department of Veterans Affairs, December 2004

Clinical Trial Phase: Phase 4 | Start Date: October 1998

Overall Status: Completed

Brief Summary

Official Title: “Verbal Memory ERPs as Indices of Treatment Response in Alzheimer Disease”

Condition Keyword(s):

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.

Study Type: Interventional

Study Design: Treatment, Non-Randomized, Open Label, Uncontrolled, Crossover Assignment, Efficacy Study

Intervention(s) in this Clinical Trial

  • Drug: Aricept
  • Drug: Exelon
  • Drug: Nicoderm Patch

Criteria for Participation in this Clinical Trial

  • 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.

Gender Eligibility for this Clinical Trial: Both

Minimum Age for this Clinical Trial: 55 Years

Maximum Age for this Clinical Trial: 85 Years

Are Healthy Volunteers Accepted for this Clinical Trial?: Accepts Healthy Volunteers

Clinical Trial Sponsor Information

Lead Sponsor: Department of Veterans Affairs

Overall Clinical Trial Officials and Contacts

Vincente Iragui, M.D., Ph.D    

Additional Information

Information obtained from ClinicalTrials.gov on July 02, 2009

Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00018278

Study ID Number: AGCG-004-98S

ClinicalTrials.gov Identifier: NCT00018278

Health Authority: United States: Federal Government

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