0 Evaluaciones
ID

22309

Descripción

Does Sleep Quality Change After Switch From Wellbutrin SR to Wellbutrin XL in Patients With Major Depressive Disorder?; ODM derived from: https://clinicaltrials.gov/show/NCT00616915

Link

https://clinicaltrials.gov/show/NCT00616915

Palabras clave

Versiones (1)
  1. 29/5/17 29/5/17 -
Subido en

29 de mayo de 2017

DOI

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Licencia

Creative Commons BY 4.0
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    Eligibility Mood Disorder NCT00616915

    Inglés

    Eligibility Mood Disorder NCT00616915

    1 formularios  
    Inclusion Criteria
    Descripción

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    1. signed patient informed consent;
    Descripción

    informed consent

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    2. patients with major depressive disorders (dsm-iv-tr - criteria used);
    Descripción

    DSM IV major depressive disorder

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C1269683
    UMLS CUI [1,2]
    C2199206
    3. out-patients;
    Descripción

    outpatients

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0029921
    4. males or females over 18 years of age;
    Descripción

    age, gender

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    UMLS CUI [2]
    C0079399
    5. patients currently using wellbutrin sr.
    Descripción

    wellbutrin sr

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0724393
    UMLS CUI [1,2]
    C0746467
    Exclusion Criteria
    Descripción

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    1. bipolar disorder patients;
    Descripción

    bipolar disorder

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0005586
    2. actively suicidal patients;
    Descripción

    actively suicidal

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0438696
    3. schizophrenia, schizoaffective or other psychotic disorder;
    Descripción

    schizophrenia, schizoaffective or other psychotic disorder

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0036341
    UMLS CUI [2]
    C0036337
    UMLS CUI [3]
    C0033975
    4. pregnant women, as by pregnancy test at the beginning of the study;
    Descripción

    pregnancy

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0032961
    5. women in childbearing age, refusing to use appropriate contraception, or breastfeeding mothers;
    Descripción

    women in childbearing age refusing to use contraception, breastfeeding mothers

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C1960468
    UMLS CUI [1,2]
    C0700589
    UMLS CUI [2]
    C0006147
    6. patients with known hypersensitivity to bupropion;
    Descripción

    hypersensitivity to bupropion

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0020517
    UMLS CUI [1,2]
    C0085208
    7. patients with severe or unstable medical conditions, which in the opinion of the investigator would interfere with their progress or safety;
    Descripción

    severe or unstable comorbidity

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0443343
    UMLS CUI [1,2]
    C0009488
    UMLS CUI [2,1]
    C0205082
    UMLS CUI [2,2]
    C0009488
    8. ect or tms treatments within the last three months;
    Descripción

    ect or tms treatment

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0013806
    UMLS CUI [2]
    C0436548
    9. patients who did not respond to previous treatment with bupropion;
    Descripción

    non-responder bupropion

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0919875
    UMLS CUI [1,2]
    C0085208
    10. patients with history of seizure disorder;
    Descripción

    seizure disorder

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0014544
    11. patients with history of eating disorders (e.g. bulimia, anorexia nervosa);
    Descripción

    eating disorders

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C0013473
    12. patients using sleep aiding medication (benzodiazepines, barbiturates).
    Descripción

    sleep aiding medication

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1]
    C2054158
    Volver a la parte superior de la página

    Similar models

    Eligibility Mood Disorder NCT00616915

    1 formularios
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    C1512693 (UMLS CUI)
    informed consent
    Item
    1. signed patient informed consent;
    boolean
    C0021430 (UMLS CUI [1])
    DSM IV major depressive disorder
    Item
    2. patients with major depressive disorders (dsm-iv-tr - criteria used);
    boolean
    C1269683 (UMLS CUI [1,1])
    C2199206 (UMLS CUI [1,2])
    outpatients
    Item
    3. out-patients;
    boolean
    C0029921 (UMLS CUI [1])
    age, gender
    Item
    4. males or females over 18 years of age;
    boolean
    C0001779 (UMLS CUI [1])
    C0079399 (UMLS CUI [2])
    wellbutrin sr
    Item
    5. patients currently using wellbutrin sr.
    boolean
    C0724393 (UMLS CUI [1,1])
    C0746467 (UMLS CUI [1,2])
    Item Group
    C0680251 (UMLS CUI)
    bipolar disorder
    Item
    1. bipolar disorder patients;
    boolean
    C0005586 (UMLS CUI [1])
    actively suicidal
    Item
    2. actively suicidal patients;
    boolean
    C0438696 (UMLS CUI [1])
    schizophrenia, schizoaffective or other psychotic disorder
    Item
    3. schizophrenia, schizoaffective or other psychotic disorder;
    boolean
    C0036341 (UMLS CUI [1])
    C0036337 (UMLS CUI [2])
    C0033975 (UMLS CUI [3])
    pregnancy
    Item
    4. pregnant women, as by pregnancy test at the beginning of the study;
    boolean
    C0032961 (UMLS CUI [1])
    women in childbearing age refusing to use contraception, breastfeeding mothers
    Item
    5. women in childbearing age, refusing to use appropriate contraception, or breastfeeding mothers;
    boolean
    C1960468 (UMLS CUI [1,1])
    C0700589 (UMLS CUI [1,2])
    C0006147 (UMLS CUI [2])
    hypersensitivity to bupropion
    Item
    6. patients with known hypersensitivity to bupropion;
    boolean
    C0020517 (UMLS CUI [1,1])
    C0085208 (UMLS CUI [1,2])
    severe or unstable comorbidity
    Item
    7. patients with severe or unstable medical conditions, which in the opinion of the investigator would interfere with their progress or safety;
    boolean
    C0443343 (UMLS CUI [1,1])
    C0009488 (UMLS CUI [1,2])
    C0205082 (UMLS CUI [2,1])
    C0009488 (UMLS CUI [2,2])
    ect or tms treatment
    Item
    8. ect or tms treatments within the last three months;
    boolean
    C0013806 (UMLS CUI [1])
    C0436548 (UMLS CUI [2])
    non-responder bupropion
    Item
    9. patients who did not respond to previous treatment with bupropion;
    boolean
    C0919875 (UMLS CUI [1,1])
    C0085208 (UMLS CUI [1,2])
    seizure disorder
    Item
    10. patients with history of seizure disorder;
    boolean
    C0014544 (UMLS CUI [1])
    eating disorders
    Item
    11. patients with history of eating disorders (e.g. bulimia, anorexia nervosa);
    boolean
    C0013473 (UMLS CUI [1])
    sleep aiding medication
    Item
    12. patients using sleep aiding medication (benzodiazepines, barbiturates).
    boolean
    C2054158 (UMLS CUI [1])
    Volver a la parte superior de la página 

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