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GEHC Has Decided Not to Provide This Detail But Will Rely on the Brief Title
The study is designed to determine the diagnostic efficacy of the visual assessment of SPECT scans in differentiating between probable dementia with Lewy Bodies (DLB) and non-DLB dementia subjects determined by the clinical diagnosis of an independent expert consensus panel used as the standard of truth.
GEHC had decided notto provide this detail
Age
55 - 90 years
Sex
ALL
Healthy Volunteers
No
Amersham Buchler GmbH Co. KG
Ismaning, Germany
Start Date
November 1, 2003
Last Updated
May 16, 2007
326
Estimated participants
DatSCAN
DRUG
Lead Sponsor
GE Healthcare
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07033494