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Clinical Trials/NCT00684281
NCT00684281
Completed
N/A

Early Diagnosis of Alzheimer's Disease: Clinical, Neuropsychological and Neuroimaging Follow-up of a Cohort of Patients With an Isolated Memory Impairment

Assistance Publique Hopitaux De Marseille1 site in 1 country60 target enrollmentJuly 2008

Overview

Phase
N/A
Intervention
Not specified
Conditions
Alzheimer's Disease
Sponsor
Assistance Publique Hopitaux De Marseille
Enrollment
60
Locations
1
Primary Endpoint
Identify the neuropsychological markers and of neuroimaging structural and metabolic useful in clinical practice which allow to predict an escalation
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The aim of this project is to follow cohort of patients with aMCI in order to establish whether there are distinct subgroups in terms of evolution or aetiology, with distinct memory profiles and profiles of mesiotemporal atrophy and metabolic change

Detailed Description

The syndrome of "amnestic Mild Cognitive Impairment" (aMCI) has been introduced for patients with intact activities of daily living, with a memory complaint and objective memory decline on neuropathological assessment, without significative change in other domains of cognition. Follow-up in these patients shows that the memory impairment may remain stable or improve, while it worsens or extends to other cognitive domains in others, indicating prodromal AD.

Registry
clinicaltrials.gov
Start Date
July 2008
End Date
December 2011
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients beforehand include in the PHRC 2001 study (These patients presented to the inclusion in the PHRC 2001 a qualified board of amnestic Mild Cognitive Impairment \[aMCI\] or light cognitive confusion of type amnestic)
  • The patient must be affiliated to an insurance scheme disease to participate in this study

Exclusion Criteria

  • For the magnetic resonance imaging: usual contraindications for an examination by MRI: claustrophobia, metal foreign bodies, pacemakers, etc.
  • Incapacitated to realize the neuropsychological evaluation because of medical intercurrentes disorders
  • Appointment of a guardian

Outcomes

Primary Outcomes

Identify the neuropsychological markers and of neuroimaging structural and metabolic useful in clinical practice which allow to predict an escalation

Time Frame: 36 months

Identify the neuropsychological markers and of neuroimaging structural and metabolic useful in clinical practice which allow to predict a stabilization or an improvement.

Time Frame: 36 months

Pursue the longitudinal study of a troop of subjects presenting an amnestic MCI in 36 months after the initial diagnosis

Time Frame: 36 months

Characterize the clinical evolution of these subjects: escalation with appearance of an insanity (of type Alzheimer's disease or of another type: degenerations fronto-temporal, insanity with body of Lewy), stabilization even improvement.

Time Frame: 36 months

Improve the state of the knowledge on the origin of the confusions mnésiques isolated at the persons of fifty and more years old.

Time Frame: 36 months

Secondary Outcomes

  • Establish diagnostic criteria which allow to improve the sensibility and the specificity of the premature diagnosis of MY.(36 months)
  • Determine if the ultra-premature diagnosis of MY at a stage where the hurts are still confined in the structures under - hippocampiques is possible.(36 months)
  • Determine the specific character or not of the infringement of the memory of visual recognition in the novice Alzheimer's disease.(36 months)
  • Determine the specific character or not the atrophy and the metabolic modifications of regions under - hippocampiques in the novice Alzheimer's disease.(36 months)
  • Inform the existence of process of functional compensation in the population of aMCI, notably to those who show themselves stable or improve.(36 months)

Study Sites (1)

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