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Clinical Trials/NCT03621839
NCT03621839RecruitingNot Applicable

New Diagnosis or Prognosis Biomarkers for Alzheimer's Disease: Biobank of CSF Collected as Part of Differential Diagnosis of Dementia

Central Hospital, Nancy, France1 site in 1 country50,000 target enrollmentStarted: July 12, 2013Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
50,000
Locations
1
Primary Endpoint
CSF collection constitution to have samples available for assessing new Alzheimer's biomarker

Study Overview

Brief Summary

Today, the Alzheimer's disease (AD) diagnosis is founded not only on clinical criteria but also on complementary examinations to confirm a physiopathological process of AD. In complex cases, lumbar punction could be necessary in order to measure Aβ peptides and Total and phosphorylated Tau but new biomarkers could be useful. The main objective of this project is to conserve these cerebrospinal fluids, collected in usual practice in order to validate new biomarkers for diagnosis, prognosis or therapeutic following of Alzheimer's disease and other dementia.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Lumbar punction collected in usual practice in the context of dementia diagnosis

Exclusion Criteria

  • Absence of consent

Outcomes

Primary Outcomes

CSF collection constitution to have samples available for assessing new Alzheimer's biomarker

Time Frame: 50 years

Each CSF collected in the context of dementia diagnosis were conserved to be used in other studies on Alzheimer's or dementia biomarkers. Futre studies that will use collected CSF to assess new biomarkers will be conduced under a new protocol describing scientific contexte, specific aims and time frame necessary to achieve them.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Central Hospital, Nancy, France
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Catherine MALAPLATE

MCU-PH

Central Hospital, Nancy, France

Study Sites (1)

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