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ID

14473

Description

The Clinical Study of Pitavastatin Treatment for Group of Mild to Moderate Alzheimer's Disease; ODM derived from: https://clinicaltrials.gov/show/NCT00548145

Lien

https://clinicaltrials.gov/show/NCT00548145

Mots-clés

Versions (1)
  1. 17/04/2016 17/04/2016 -
Téléchargé le

17 avril 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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    Eligibility Alzheimer Disease NCT00548145

    Anglais

    Eligibility Alzheimer Disease NCT00548145

    1 Formulaires  
    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    alzheimer's disease patients (15 ≤ mmse total score ≤ 23, cdr "1" or "2")
    Description

    Mini-mental state examination; alzheimers disease

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0451306
    UMLS CUI [2]
    C0002395
    patients with hypercholesterolemia
    Description

    hypercholesterolemia

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0020443
    patients who have taken donepezil more than 3 months stably
    Description

    donepezil

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0527316
    both patients and care-givers must be more than 20 years old
    Description

    age

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    Exclusion Criteria
    Description

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    women with pregnancy or breast-feeding
    Description

    pregnancy; lactating

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0032961
    UMLS CUI [1,2]
    C0006147
    malignant tumor
    Description

    malignant tumor

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0006826
    cerebrovascular disorder or myocardial infarction prior to 12 weeks
    Description

    cerebrovascular disorder; myocardial infarction

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0007820
    UMLS CUI [2]
    C0027051
    heart failure [new york heart association (nyha) class iii or iv]
    Description

    heart failure; NYHA classification

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0018801
    UMLS CUI [2]
    C1275491
    hepatic or renal dysfunction
    Description

    hepatic dysfunction; renal dysfunction

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0086565
    UMLS CUI [2]
    C3279454
    severe hypertension
    Description

    hypertension

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0020538
    hypothyroidism, hereditary muscular disease, history of drug-induced myopathy
    Description

    hypothyroidism; muscular disease hereditary; drug-induced myopathy

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0020676
    UMLS CUI [2,1]
    C0026848
    UMLS CUI [2,2]
    C0439660
    UMLS CUI [3]
    C0410220
    current involvement in another investigational drug study
    Description

    Study Subject Participation Status

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C2348568
    alcoholism, drug abuse
    Description

    Substance Use Disorder

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0038586
    Retour au début de la page

    Similar models

    Eligibility Alzheimer Disease NCT00548145

    1 Formulaires
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Mini-mental state examination; alzheimers disease
    Item
    alzheimer's disease patients (15 ≤ mmse total score ≤ 23, cdr "1" or "2")
    boolean
    C0451306 (UMLS CUI [1])
    C0002395 (UMLS CUI [2])
    hypercholesterolemia
    Item
    patients with hypercholesterolemia
    boolean
    C0020443 (UMLS CUI [1])
    donepezil
    Item
    patients who have taken donepezil more than 3 months stably
    boolean
    C0527316 (UMLS CUI [1])
    age
    Item
    both patients and care-givers must be more than 20 years old
    boolean
    C0001779 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    pregnancy; lactating
    Item
    women with pregnancy or breast-feeding
    boolean
    C0032961 (UMLS CUI [1,1])
    C0006147 (UMLS CUI [1,2])
    malignant tumor
    Item
    malignant tumor
    boolean
    C0006826 (UMLS CUI [1])
    cerebrovascular disorder; myocardial infarction
    Item
    cerebrovascular disorder or myocardial infarction prior to 12 weeks
    boolean
    C0007820 (UMLS CUI [1])
    C0027051 (UMLS CUI [2])
    heart failure; NYHA classification
    Item
    heart failure [new york heart association (nyha) class iii or iv]
    boolean
    C0018801 (UMLS CUI [1])
    C1275491 (UMLS CUI [2])
    hepatic dysfunction; renal dysfunction
    Item
    hepatic or renal dysfunction
    boolean
    C0086565 (UMLS CUI [1])
    C3279454 (UMLS CUI [2])
    hypertension
    Item
    severe hypertension
    boolean
    C0020538 (UMLS CUI [1])
    hypothyroidism; muscular disease hereditary; drug-induced myopathy
    Item
    hypothyroidism, hereditary muscular disease, history of drug-induced myopathy
    boolean
    C0020676 (UMLS CUI [1])
    C0026848 (UMLS CUI [2,1])
    C0439660 (UMLS CUI [2,2])
    C0410220 (UMLS CUI [3])
    Study Subject Participation Status
    Item
    current involvement in another investigational drug study
    boolean
    C2348568 (UMLS CUI [1])
    Substance Use Disorder
    Item
    alcoholism, drug abuse
    boolean
    C0038586 (UMLS CUI [1])
    Retour au début de la page 

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