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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06164938
Other study ID # FDG-NORM
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 14, 2010
Est. completion date January 12, 2011

Study information

Verified date December 2023
Source IRCCS San Raffaele
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the study is to obtain information on cerebral glucose metabolism measured with the 18F-FDG PET technique in normal subjects without current or previous neurological or psychiatric pathologies in order to use the data obtained for voxel-based statistical analyzes for comparison with individual subjects ( patients with disease neurological or psychiatric) which will be evaluated with the same method to improve the specificity and diagnostic sensitivity of the FDG PET exam. The objective is to obtain a functional measure of brain glucose metabolism in every normal subject because this is a functional measure of brain activity. The subjects will represent different decades of age to have a wider range of comparison with patients.


Recruitment information / eligibility

Status Completed
Enrollment 23
Est. completion date January 12, 2011
Est. primary completion date January 12, 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 40 Years to 80 Years
Eligibility Inclusion Criteria: - absence of neurological and psychiatric pathologies, negative pregnancy test.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Diagnostic accuracy
The aim is to obtain a regional measure of brain glucose metabolism in each normal subject because this is a functional measure of brain activity.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
IRCCS San Raffaele

Outcome

Type Measure Description Time frame Safety issue
Primary Study of glucose metabolism with 18 F FDG PET Study of glucose metabolism with 18 F FDG PET in normal subjects without current or previous neurological or psychiatric pathologies in order to use the data obtained for statistical analyzes for comparison with individual subjects (patients with neurological or psychiatric) which will be evaluated with the same method to improve the diagnostic sensitivity of the FDG PET exam. 1 year
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