- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT01465360
Performance of AclarusDx™, a Blood-Based Transcriptomic Test for AD, in US Patients Newly Referred to a Memory Center
Performance of AclarusDx™, A Blood-Based Transcriptomic Test for Alzheimer's Disease, in US-based Patients Suffering From Memory Impairment and Newly Referred to A Reference Memory Center, for AD Diagnostic Workup-A Pilot Descriptive Study
Aperçu de l'étude
Statut
Description détaillée
The objective of this study is to apply AclarusDx™ signature in a reference US Center in 160 patients newly referred to one of the three study centers within the Cleveland Clinic, Center for Brain Health network, for diagnostic workup. Only AclarusDx™ will be added to the panel of tests usually performed at the centers to establish diagnosis. AclarusDx™ will be used for investigational use only, not for diagnostic purpose. The ultimate goal is to define the clinical utility of AclarusDx™ to provide Primary Care Physicians (PCPs) with a tool that will help them in making the diagnosis of Alzheimer's Disease (AD).
The primary objectives are :
- To obtain an estimate of the capability of AclarusDx™ to identify AD patients among a US-based population of newly referred patients suffering from objective memory impairment which maybe potentially related to multiple and different etiologies.
- To compare the performance of AclarusDx™ in a US-based population of newly referred patients with memory impairment with the performance of AclarusDx™ observed in one comparable European population.
Type d'étude
Inscription (Réel)
Contacts et emplacements
Lieux d'étude
-
-
Nevada
-
Las Vegas, Nevada, États-Unis, 89106
- Cleveland Clinic Lou Ruvo Center for Brain Health
-
-
Ohio
-
Cleveland, Ohio, États-Unis, 44195
- Cleveland Clinic Center for Brain Health - Mellen Center
-
Lakewood, Ohio, États-Unis, 44107
- Cleveland Clinic Senior Care Assessment - Lakewood Hospital
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
Méthode d'échantillonnage
Population étudiée
La description
Inclusion Criteria:
- Male or female patient referred to the center for memory impairment.
- The memory impairment has previously been observed by a caregiver or documented by a physician.
- The memory impairment is confirmed by the memory center.
- Caucasian ethnicity.
- A written informed consent approved by an ethical review board or similar body must be obtained from the patient prior to any study-related procedures.
- If applicable, standard treatment with cholinesterase inhibitor and/or memantine is acceptable.
- Patient estimated to be compliant with study procedures.
- Patient has a level of understanding sufficient to agree to all procedures required by the protocol and must be able to cooperate. Under no circumstances will a subject who does not understand the procedure, be allowed to consent to the procedure.
Exclusion Criteria:
- Recent acute pathology or medical condition or surgery which may alter the inflammatory homeostasis, according to the opinion of the investigator.
- Non-Caucasian ethnicity.
- Patient with severe uncontrolled or unstable medical condition.
- Need for a legal representative for the medical condition of the patient.
- Any current pathology or medical condition, for which blood sampling may involve a risk for the patient's health, according to the opinion of the investigator.
- Current or recent history (within one month) of clinically significant pathology, medical condition (including hospitalization) or symptoms. However, chronic diseases or medical conditions that are considered stable are accepted, provided that they are compatible with other study selection criteria.
- Current or recent history of drug or alcohol abuse or dependence.
- Current, clinically significant major psychiatric disorder (eg, major depressive disorder) according to the Diagnostic and Statistical Manual of Mental Disorders, 4th Edition text revised (DSM-IV TR), or significant symptoms (eg, hallucinations).
- Woman of childbearing potential is not allowed to participate in the study. (A woman of childbearing potential is a woman who is biologically capable of becoming pregnant).
- Current participation in another study using an investigational non-marketed product.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Cohortes et interventions
Groupe / Cohorte |
|---|
|
Study patients
Patients newly referred to a Reference Memory Center with a complaint of memory impairment for AD diagnostic workup.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Sensitivity of AclarusDx™ in AD patients
Délai: Outcome measured during one single study visit
|
The determination of the sensitivity of the test, being the percentage of positive AclarusDx™ calls among referred patients being confirmed clinically as having AD at the Memory Center will be calculated.
|
Outcome measured during one single study visit
|
Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Charles B. Bernick, MD, Cleveland Clinic Lou Ruvo Center for Brain Health
Publications et liens utiles
Liens utiles
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
- Les troubles mentaux
- Maladies cardiovasculaires
- Maladies vasculaires
- Maladies métaboliques
- Troubles cérébrovasculaires
- Maladies du cerveau
- Maladies du système nerveux central
- Maladies du système nerveux
- Artériosclérose
- Maladies artérielles occlusives
- Manifestations neurologiques
- Manifestations neurocomportementales
- Troubles neurocognitifs
- Troubles parkinsoniens
- Maladies des noyaux gris centraux
- Troubles du mouvement
- Synucleinopathies
- Maladies neurodégénératives
- TDP-43 Protéinopathies
- Déficits de protéostase
- Tauopathies
- Troubles cognitifs
- Troubles du langage
- Troubles de la communication
- Maladies artérielles intracrâniennes
- Troubles de la parole
- Dégénérescence lobaire frontotemporale
- Artériosclérose intracrânienne
- Leucoencéphalopathies
- Maladie de Parkinson
- Démence
- Maladie d'Alzheimer
- Dysfonctionnement cognitif
- Aphasie
- Démence frontotemporale
- Aphasie primaire progressive
- Choisissez la maladie du cerveau
- Démence vasculaire
Autres numéros d'identification d'étude
- EHTAD/003
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .
Essais cliniques sur Déficience cognitive légère
-
Foundation University IslamabadRecrutementDysfonctionnement cognitif | Déclin cognitif | Trouble cognitifPakistan
-
National Taiwan University HospitalNational Taiwan Science Education Center(NTSEC)ComplétéEntraînement cognitif | Déclin cognitif subjectifTaïwan
-
Foundation University IslamabadRecrutementDéclin cognitif | Trouble cognitif | Troubles cognitifsPakistan
-
China Medical University HospitalPas encore de recrutementDéclin cognitif subjectif | Déclin cognitif subjectif (SCD)Taïwan
-
Rotman Research Institute at BaycrestRecrutementTrouble cognitif léger (MCI) | Déclin cognitif subjectif (SCD)Canada
-
University of Social Sciences and Humanities, WarsawNational Science Centre, Poland; Sanprobi Sp. z o. o.Actif, ne recrute pasDéclin cognitif | Vieillissement cognitif | Déclin de la mémoirePologne
-
Rotman Research Institute at BaycrestSunnybrook Health Sciences Centre; University of Waterloo; Toronto Rehabilitation... et autres collaborateursRésiliéDéclin cognitif subjectif | Déclin cognitif lié à l'âgeCanada
-
University of MiamiComplété
-
The Hong Kong Polytechnic UniversityRecrutementDéclin cognitif subjectifChine
-
University Hospital TuebingenPas encore de recrutementDéclin cognitif subjectifAllemagne