CompletedNCT00938665
Evaluation of a Handheld Event Related Potential (ERP)/Quantitative Electroencephalography (qEEG) System (COGNISION™) as a Useful Cognitive Biomarker for Alzheimer's Disease.
Studying Frontotemporal dementia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Neuronetrix, Inc.
- Principal Investigator
- Charles D Smith, MD, M.DUniveristy of Kentucky
- Intervention
- COGNISION™ System(device)
- Enrollment
- 204 enrolled
- Eligibility
- 60-90 years · All sexes
- Timeline
- 2010 – 2014
Study locations (7)
- Premiere Research Institute, West Palm Beach, Florida, United States
- University of Kentucky, Lexington, Kentucky, United States
- Norton Healthcare, Louisville, Kentucky, United States
- Boston Center for Memory, Brookline, Massachusetts, United States
- Duke University, Durham, North Carolina, United States
- University of Pennsylvania, Philadelphia, Pennsylvania, United States
- The Memory Clinic, Bennington, Vermont, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT00938665 on ClinicalTrials.govOther trials for Frontotemporal dementia
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