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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01565434
Other study ID # PA11014
Secondary ID
Status Completed
Phase N/A
First received March 26, 2012
Last updated June 8, 2016
Start date February 2012
Est. completion date April 2015

Study information

Verified date March 2012
Source CHU de Reims
Contact n/a
Is FDA regulated No
Health authority France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Study type Interventional

Clinical Trial Summary

Main objective: investigate whether a functional polymorphism of CR1 (length, number of binding sites in C4b C3b, erythrocyte density, rate of soluble CR1 ...) so determined genetic or acquired, is a susceptibility factor for the disease Alzheimer's.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date April 2015
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- caucasians people with a Alzheimer dementia defined on DSMIV criteria for patients and without Alzheimer disease for control subjects

Exclusion Criteria:

- diseases modifying CR1 physiology

Study Design

Primary Purpose: Screening


Related Conditions & MeSH terms


Intervention

Other:
CR1 impact


Locations

Country Name City State
France CHU de REIMS Reims

Sponsors (1)

Lead Sponsor Collaborator
CHU de Reims

Country where clinical trial is conducted

France, 

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