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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05831371
Other study ID # 2023PI065
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date May 2, 2023
Est. completion date September 2, 2023

Study information

Verified date April 2023
Source Central Hospital, Nancy, France
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Etiology and cognitive prognosis in late onset epilepsy differ from young adults epilepsy. At the epilepsy onset, this is crucial to detect potential curative/treatable brain disorders. After classical investigation including morphological brain imaging, EEG, clinical assessment, which added value may have brain FDG PET in the diagnosis and prognosis evaluation?


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 87
Est. completion date September 2, 2023
Est. primary completion date August 2, 2023
Accepts healthy volunteers No
Gender All
Age group 60 Years and older
Eligibility Inclusion Criteria: - late onset épilepsy patients without lesion - epilepsy followed at the CHRU Nancy france Exclusion Criteria: - epilepsy explained by cortical lesion - severe psychiatric disorders - severe addiction (alcool, drugs) - no FDG TEP performed - no neuropsychological assessement after 2 years epilepsy onset

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
TEP FDG
FDG TEP peformed in clinical routine

Locations

Country Name City State
France CHRU Nancy Nancy

Sponsors (1)

Lead Sponsor Collaborator
Central Hospital, Nancy, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary diagnostic performances sensibility, specificty, accurracy 2 years after epilepsy onset
Secondary cognitive prognosis performances sensibility, specificty, accurracy 2 years after epilepsy onset
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