0 Beoordelingen
ID

15072

Beschrijving

A Study to Evaluate the Efficacy and Safety of Galantamine in Patients With Mild Cognitive Impairment; ODM derived from: https://clinicaltrials.gov/show/NCT00236431

Link

https://clinicaltrials.gov/show/NCT00236431

Trefwoorden

Versies (2)
  1. 13-05-16 13-05-16 -
  2. 14-05-16 14-05-16 -
Geüploaded op

14 mei 2016

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

  • Nieuwste
  • Oudste
  • Populair
  • Nieuwste
    • Nieuwste
    • Oudste
    • Populair

    Geen commentaren

    U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

    Eligibility Dementia NCT00236431

    Engels

    Eligibility Dementia NCT00236431

    1 Formulieren  
    1. StudyEvent: Eligibility
      1. Eligibility Dementia NCT00236431
    Inclusion Criteria
    Beschrijving

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    clinical decline of cognitive ability consistent with mild cognitive impairment
    Beschrijving

    mild cognitive impairment

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C0497327
    UMLS CUI [1,2]
    C0439793
    delayed recall score <= 10 on a new york university paragraph recall test
    Beschrijving

    memory test

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0451476
    sufficient visual, hearing and communication capabilities and be willing to complete serial standard tests of cognitive function
    Beschrijving

    visual, hearing and communication capabilities; willing to complete serial standard tests of cognitive function

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C3665347
    UMLS CUI [2]
    C0018767
    UMLS CUI [3]
    C0009452
    have a consistent informant to accompany them on scheduled visits
    Beschrijving

    informant for visits

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C1552519
    UMLS CUI [1,2]
    C0545082
    be able to read, write and fully understand the language of the cognitive scales used in the study
    Beschrijving

    language abilities

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0586739
    UMLS CUI [2]
    C0584992
    UMLS CUI [3]
    C1145677
    Exclusion Criteria
    Beschrijving

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    neurodegenerative disorders such as parkinson's disease
    Beschrijving

    neurodegenerative disorder

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0524851
    cognitive impairment resulting from acute cerebral trauma, hypoxic cerebral damage, vitamin deficiency states, infections such as meningitis or aids, or primary or metastatic cerebral neoplasia
    Beschrijving

    cognitive impairment resulting from acute cerebral trauma, hypoxic cerebral damage, vitamin deficiency states, infections such as meningitis or aids, or primary or metastatic cerebral neoplasia

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C1839000
    UMLS CUI [1,2]
    C0558400
    UMLS CUI [2,1]
    C1839000
    UMLS CUI [2,2]
    C0242184
    UMLS CUI [2,3]
    C0006104
    UMLS CUI [3,1]
    C1839000
    UMLS CUI [3,2]
    C1510471
    UMLS CUI [4,1]
    C1839000
    UMLS CUI [4,2]
    C0009450
    UMLS CUI [5,1]
    C1839000
    UMLS CUI [5,2]
    C1882062
    UMLS CUI [5,3]
    C0006104
    epilepsy
    Beschrijving

    epilepsy

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0014544
    significant psychiatric disease
    Beschrijving

    psychiatric disease

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0004936
    peptic ulcer disease
    Beschrijving

    peptic ulcer

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0030920
    clinically significant heart, lung, liver or kidney diseases
    Beschrijving

    heart, lung, liver or kidney diseases

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0018799
    UMLS CUI [2]
    C0024115
    UMLS CUI [3]
    C0023895
    UMLS CUI [4]
    C0022658
    pregnant or nursing women or those without adequate contraception
    Beschrijving

    Fertility, breast feeding; Contraception

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C0015895
    UMLS CUI [2]
    C0032961
    UMLS CUI [3]
    C0006147
    Terug naar het begin van de pagina

    Similar models

    Eligibility Dementia NCT00236431

    1 Formulieren
    1. StudyEvent: Eligibility
      1. Eligibility Dementia NCT00236431
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    C1512693 (UMLS CUI)
    mild cognitive impairment
    Item
    clinical decline of cognitive ability consistent with mild cognitive impairment
    boolean
    C0497327 (UMLS CUI [1,1])
    C0439793 (UMLS CUI [1,2])
    memory test
    Item
    delayed recall score <= 10 on a new york university paragraph recall test
    boolean
    C0451476 (UMLS CUI [1])
    visual, hearing and communication capabilities; willing to complete serial standard tests of cognitive function
    Item
    sufficient visual, hearing and communication capabilities and be willing to complete serial standard tests of cognitive function
    boolean
    C3665347 (UMLS CUI [1])
    C0018767 (UMLS CUI [2])
    C0009452 (UMLS CUI [3])
    informant for visits
    Item
    have a consistent informant to accompany them on scheduled visits
    boolean
    C1552519 (UMLS CUI [1,1])
    C0545082 (UMLS CUI [1,2])
    language abilities
    Item
    be able to read, write and fully understand the language of the cognitive scales used in the study
    boolean
    C0586739 (UMLS CUI [1])
    C0584992 (UMLS CUI [2])
    C1145677 (UMLS CUI [3])
    Item Group
    C0680251 (UMLS CUI)
    neurodegenerative disorder
    Item
    neurodegenerative disorders such as parkinson's disease
    boolean
    C0524851 (UMLS CUI [1])
    cognitive impairment resulting from acute cerebral trauma, hypoxic cerebral damage, vitamin deficiency states, infections such as meningitis or aids, or primary or metastatic cerebral neoplasia
    Item
    cognitive impairment resulting from acute cerebral trauma, hypoxic cerebral damage, vitamin deficiency states, infections such as meningitis or aids, or primary or metastatic cerebral neoplasia
    boolean
    C1839000 (UMLS CUI [1,1])
    C0558400 (UMLS CUI [1,2])
    C1839000 (UMLS CUI [2,1])
    C0242184 (UMLS CUI [2,2])
    C0006104 (UMLS CUI [2,3])
    C1839000 (UMLS CUI [3,1])
    C1510471 (UMLS CUI [3,2])
    C1839000 (UMLS CUI [4,1])
    C0009450 (UMLS CUI [4,2])
    C1839000 (UMLS CUI [5,1])
    C1882062 (UMLS CUI [5,2])
    C0006104 (UMLS CUI [5,3])
    epilepsy
    Item
    epilepsy
    boolean
    C0014544 (UMLS CUI [1])
    psychiatric disease
    Item
    significant psychiatric disease
    boolean
    C0004936 (UMLS CUI [1])
    peptic ulcer
    Item
    peptic ulcer disease
    boolean
    C0030920 (UMLS CUI [1])
    heart, lung, liver or kidney diseases
    Item
    clinically significant heart, lung, liver or kidney diseases
    boolean
    C0018799 (UMLS CUI [1])
    C0024115 (UMLS CUI [2])
    C0023895 (UMLS CUI [3])
    C0022658 (UMLS CUI [4])
    Fertility, breast feeding; Contraception
    Item
    pregnant or nursing women or those without adequate contraception
    boolean
    C0015895 (UMLS CUI [1])
    C0032961 (UMLS CUI [2])
    C0006147 (UMLS CUI [3])
    Terug naar het begin van de pagina 

    Help

    Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

    Watch Tutorial