0 Avaliações
ID

25113

Descrição

Study ID: 100013 Clinical Study ID: RRL100013 A 12-Week, Double-Blind, Placebo-Controlled, Twice-Daily Dosing Study to Assess the Efficacy and Safety of Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS) Requiring Extended Treatment Coverage

Palavras-chave

Versões (2)
  1. 26/08/2017 26/08/2017 -
  2. 17/09/2021 17/09/2021 -
Titular dos direitos

gsk

Transferido a

26 de agosto de 2017

DOI

Para um pedido faça login.

Licença

Creative Commons BY-NC 3.0
Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Voltar para os comentários do modelo
Comentários do grupo de itens para :

Comentários do item para :

  • Os mais recentes
  • Os mais antigos
  • Preferidos
  • Os mais recentes
    • Os mais recentes
    • Os mais antigos
    • Preferidos

    Sem comentários

    Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

    TIME AND EVENTS TABLE Ropinirole Case Report Form GSK RRL100013

    Alemão Inglês

    TIME AND EVENTS TABLE Ropinirole Case Report Form GSK

    1 Formulários  
    TIME AND EVENTS TABLE
    Descrição

    TIME AND EVENTS TABLE

    Assessments
    Descrição

    Assessments

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C0220825
    IRLSSG diagnostic criteria
    Descrição

    IRLSSG diagnostic criteria

    Tipo de dados

    integer

    Alias
    UMLS CUI [1,1]
    C0035258
    UMLS CUI [1,2]
    C2348561
    Inclusion/exclusion criteria
    Descrição

    Inclusion/exclusion criteria

    Tipo de dados

    integer

    Alias
    UMLS CUI [1,1]
    C1512693
    UMLS CUI [1,2]
    C0680251
    Subject demography
    Descrição

    Subject demography

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C0011298
    RLS history
    Descrição

    RLS history

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C0035258
    Orthostatic blood pressure and heart rate
    Descrição

    Orthostatic blood pressure and heart rate

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C1095971
    Weight
    Descrição

    Weight

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C0220825
    Height
    Descrição

    Height

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C0005890
    ECG
    Descrição

    ECG

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C0220825
    Medical/surgical history
    Descrição

    Medical/surgical history

    Tipo de dados

    integer

    Alias
    UMLS CUI [1,1]
    C0262926
    UMLS CUI [1,2]
    C0455610
    Physical examination
    Descrição

    Physical examination

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C0031809
    Laboratory evaluation
    Descrição

    Laboratory evaluation

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C0022885
    Prior/concomitant medication
    Descrição

    Prior/concomitant medication

    Tipo de dados

    integer

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0013227
    Pregnancy test
    Descrição

    Pregnancy test

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C0032976
    Dispense Subject Symptom Diary
    Descrição

    Dispense Subject Symptom Diary

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C2216446
    Dispense Actigraphy device
    Descrição

    Dispense Actigraphy device

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C1171301
    IRLS Rating Scale
    Descrição

    IRLS Rating Scale

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C0681889
    CGI Scales (Improvement & Severity)
    Descrição

    CGI Scales (Improvement & Severity)

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C3639708
    Insomnia Severity Index
    Descrição

    Insomnia Severity Index

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C0917801
    Written informed consent
    Descrição

    Written informed consent

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C0021430
    Dispense Patient Global Improvement Scale (PGI) Forms
    Descrição

    Dispense Patient Global Improvement Scale (PGI) Forms

    Tipo de dados

    integer

    Alias
    UMLS CUI [1,1]
    C2986411
    UMLS CUI [1,2]
    C0349674
    Patient satisfaction question
    Descrição

    Patient satisfaction question

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C3476649
    Quality of Life Questionnaire
    Descrição

    Quality of Life Questionnaire

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C0451149
    MOS Sleep Scale
    Descrição

    MOS Sleep Scale

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C3697468
    Profile of Mood States (POMS)
    Descrição

    Profile of Mood States (POMS)

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C0451394
    Hospital Anxiety and Depression Scale (HADS)
    Descrição

    Hospital Anxiety and Depression Scale (HADS)

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C0451221
    Adverse events
    Descrição

    Adverse events

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C0877248
    Subject randomization
    Descrição

    Subject randomization

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C0034656
    Pharmacogenomics sample
    Descrição

    Pharmacogenomics sample

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C1138555
    Study conclusion form
    Descrição

    Study conclusion form

    Tipo de dados

    integer

    Alias
    UMLS CUI [1]
    C1707478
    Voltar ao início da página

    Similar models

    TIME AND EVENTS TABLE Ropinirole Case Report Form GSK

    1 Formulários
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de dados
    Alias
    Item Group
    TIME AND EVENTS TABLE
    Item
    Assessments
    integer
    C0220825 (UMLS CUI [1])
    Assessments
    Code List
    Assessments
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    IRLSSG diagnostic criteria
    integer
    C0035258 (UMLS CUI [1,1])
    C2348561 (UMLS CUI [1,2])
    Assessments
    Code List
    IRLSSG diagnostic criteria
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Inclusion/exclusion criteria
    integer
    C1512693 (UMLS CUI [1,1])
    C0680251 (UMLS CUI [1,2])
    Assessments
    Code List
    Inclusion/exclusion criteria
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Subject demography
    integer
    C0011298 (UMLS CUI [1])
    Assessments
    Code List
    Subject demography
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    RLS history
    integer
    C0035258 (UMLS CUI [1])
    Assessments
    Code List
    RLS history
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Orthostatic blood pressure and heart rate
    integer
    C1095971 (UMLS CUI [1])
    Assessments
    Code List
    Orthostatic blood pressure and heart rate
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Weight
    integer
    C0220825 (UMLS CUI [1])
    Assessments
    Code List
    Weight
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Height
    integer
    C0005890 (UMLS CUI [1])
    Assessments
    Code List
    Height
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    ECG
    integer
    C0220825 (UMLS CUI [1])
    Assessments
    Code List
    ECG
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Medical/surgical history
    integer
    C0262926 (UMLS CUI [1,1])
    C0455610 (UMLS CUI [1,2])
    Assessments
    Code List
    Medical/surgical history
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Physical examination
    integer
    C0031809 (UMLS CUI [1])
    Assessments
    Code List
    Physical examination
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Laboratory evaluation
    integer
    C0022885 (UMLS CUI [1])
    Assessments
    Code List
    Laboratory evaluation
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Prior/concomitant medication
    integer
    C2347852 (UMLS CUI [1,1])
    C0013227 (UMLS CUI [1,2])
    Assessments
    Code List
    Prior/concomitant medication
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Pregnancy test
    integer
    C0032976 (UMLS CUI [1])
    Assessments
    Code List
    Pregnancy test
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Dispense Subject Symptom Diary
    integer
    C2216446 (UMLS CUI [1])
    Assessments
    Code List
    Dispense Subject Symptom Diary
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Dispense Actigraphy device
    integer
    C1171301 (UMLS CUI [1])
    Assessments
    Code List
    Dispense Actigraphy device
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    IRLS Rating Scale
    integer
    C0681889 (UMLS CUI [1])
    Assessments
    Code List
    IRLS Rating Scale
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    CGI Scales (Improvement & Severity)
    integer
    C3639708 (UMLS CUI [1])
    Assessments
    Code List
    CGI Scales (Improvement & Severity)
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Insomnia Severity Index
    integer
    C0917801 (UMLS CUI [1])
    Assessments
    Code List
    Insomnia Severity Index
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Written informed consent
    integer
    C0021430 (UMLS CUI [1])
    Assessments
    Code List
    Written informed consent
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Dispense Patient Global Improvement Scale (PGI) Forms
    integer
    C2986411 (UMLS CUI [1,1])
    C0349674 (UMLS CUI [1,2])
    Assessments
    Code List
    Dispense Patient Global Improvement Scale (PGI) Forms
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Patient satisfaction question
    integer
    C3476649 (UMLS CUI [1])
    Assessments
    Code List
    Patient satisfaction question
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Quality of Life Questionnaire
    integer
    C0451149 (UMLS CUI [1])
    Assessments
    Code List
    Quality of Life Questionnaire
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    MOS Sleep Scale
    integer
    C3697468 (UMLS CUI [1])
    Assessments
    Code List
    MOS Sleep Scale
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Profile of Mood States (POMS)
    integer
    C0451394 (UMLS CUI [1])
    Assessments
    Code List
    Profile of Mood States (POMS)
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Hospital Anxiety and Depression Scale (HADS)
    integer
    C0451221 (UMLS CUI [1])
    Assessments
    Code List
    Hospital Anxiety and Depression Scale (HADS)
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Adverse events
    integer
    C0877248 (UMLS CUI [1])
    Assessments
    Code List
    Adverse events
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Subject randomization
    integer
    C0034656 (UMLS CUI [1])
    Assessments
    Code List
    Subject randomization
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Pharmacogenomics sample
    integer
    C1138555 (UMLS CUI [1])
    Assessments
    Code List
    Pharmacogenomics sample
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Item
    Study conclusion form
    integer
    C1707478 (UMLS CUI [1])
    Assessments
    Code List
    Study conclusion form
    CL Item
    Screening (1)
    C1409616 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Baseline (2)
    C1442488 (UMLS CUI-1)
    (Comment:en)
    CL Item
    12 Week Double-Blind Treatment Phase (3)
    C0013072 (UMLS CUI-1)
    C0814495 (UMLS CUI-2)
    (Comment:en)
    CL Item
    Early withdrawal (4)
    C2349954 (UMLS CUI-1)
    (Comment:en)
    CL Item
    Follow Up (5)
    C1522577 (UMLS CUI-1)
    (Comment:en)
    Voltar ao início da página 

    Ajuda

    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