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ID

13194

Description

Dichotic Listening as a Predictor of Medication Response in Depression; ODM derived from: https://clinicaltrials.gov/show/NCT00296725

Lien

https://clinicaltrials.gov/show/NCT00296725

Mots-clés

Versions (1)
  1. 23/01/2016 23/01/2016 -
Téléchargé le

23 janvier 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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    Eligibility Major Depression NCT00296725

    Anglais

    Eligibility Major Depression NCT00296725

    1 Formulaires  
    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    ages between 18-65
    Description

    Age

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    meets dsm-iv criteria for current major depression, dysthymia or depression nos
    Description

    major depression, dysthymia or depression nos

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C1269683
    UMLS CUI [2]
    C0013415
    UMLS CUI [3]
    C0011581
    Exclusion Criteria
    Description

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    known hearing impairment
    Description

    hearing impairment

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C1384666
    active suicidal ideation (history of suicide attempts will be evaluated on a case by case basis)
    Description

    Suicidality

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0438696
    hamd > 20
    Description

    hamd

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0451203
    current (past six months) alcohol and/or drug abuse or dependence
    Description

    alcohol and/or drug abuse or dependence

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0038586
    medical condition likely to require intervention contraindicated with study medication (e.g., known arrhythmia likely to be exacerbated by imipramine)
    Description

    medical condition contraindicated with study medication

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0009488
    bipolar i
    Description

    bipolar i

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0005586
    UMLS CUI [2]
    C0853193
    psychosis
    Description

    psychosis

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0033975
    if currently taking antidepressants or mood stabilizers, cannot be off psychotropic medication for 7 weeks (10 weeks for prozac) or felt to require other psychiatric medication (other than occasional sleep or anxiety medication)
    Description

    psychatric medication

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0003289
    UMLS CUI [2]
    C4020582
    UMLS CUI [3]
    C0748066
    premenopausal women not using known effective birth control
    Description

    birth control

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0700589
    not currently depressed (whether considered due to current treatment or not)
    Description

    not currently depressed

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0344315
    UMLS CUI [2]
    C0011570
    nonresponse to adequate trial of both study medications (i.e., > 4weeks on > escitalopram 30 mg/d, and imipramine 200 mg/d); patients having an inadequate response to one study medication could be enrolled and receive the other; patients having responded to an adequate trial of either study medication would be offered a retrial; also excluded will be subjects having non responded to an adequate trial with citalopram (i.e., > 4 weeks on > citalopram 60 mg/d)
    Description

    response to treatment, escitalporam, imipramine

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0521982
    UMLS CUI [2]
    C1099456
    UMLS CUI [3]
    C0020934
    left-handed
    Description

    left handed

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0234418
    Retour au début de la page

    Similar models

    Eligibility Major Depression NCT00296725

    1 Formulaires
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Age
    Item
    ages between 18-65
    boolean
    C0001779 (UMLS CUI [1])
    major depression, dysthymia or depression nos
    Item
    meets dsm-iv criteria for current major depression, dysthymia or depression nos
    boolean
    C1269683 (UMLS CUI [1])
    C0013415 (UMLS CUI [2])
    C0011581 (UMLS CUI [3])
    Item Group
    C0680251 (UMLS CUI)
    hearing impairment
    Item
    known hearing impairment
    boolean
    C1384666 (UMLS CUI [1])
    Suicidality
    Item
    active suicidal ideation (history of suicide attempts will be evaluated on a case by case basis)
    boolean
    C0438696 (UMLS CUI [1])
    hamd
    Item
    hamd > 20
    boolean
    C0451203 (UMLS CUI [1])
    alcohol and/or drug abuse or dependence
    Item
    current (past six months) alcohol and/or drug abuse or dependence
    boolean
    C0038586 (UMLS CUI [1])
    medical condition contraindicated with study medication
    Item
    medical condition likely to require intervention contraindicated with study medication (e.g., known arrhythmia likely to be exacerbated by imipramine)
    boolean
    C0009488 (UMLS CUI [1])
    bipolar i
    Item
    bipolar i
    boolean
    C0005586 (UMLS CUI [1])
    C0853193 (UMLS CUI [2])
    psychosis
    Item
    psychosis
    boolean
    C0033975 (UMLS CUI [1])
    psychatric medication
    Item
    if currently taking antidepressants or mood stabilizers, cannot be off psychotropic medication for 7 weeks (10 weeks for prozac) or felt to require other psychiatric medication (other than occasional sleep or anxiety medication)
    boolean
    C0003289 (UMLS CUI [1])
    C4020582 (UMLS CUI [2])
    C0748066 (UMLS CUI [3])
    birth control
    Item
    premenopausal women not using known effective birth control
    boolean
    C0700589 (UMLS CUI [1])
    not currently depressed
    Item
    not currently depressed (whether considered due to current treatment or not)
    boolean
    C0344315 (UMLS CUI [1])
    C0011570 (UMLS CUI [2])
    response to treatment, escitalporam, imipramine
    Item
    nonresponse to adequate trial of both study medications (i.e., > 4weeks on > escitalopram 30 mg/d, and imipramine 200 mg/d); patients having an inadequate response to one study medication could be enrolled and receive the other; patients having responded to an adequate trial of either study medication would be offered a retrial; also excluded will be subjects having non responded to an adequate trial with citalopram (i.e., > 4 weeks on > citalopram 60 mg/d)
    boolean
    C0521982 (UMLS CUI [1])
    C1099456 (UMLS CUI [2])
    C0020934 (UMLS CUI [3])
    left handed
    Item
    left-handed
    boolean
    C0234418 (UMLS CUI [1])
    Retour au début de la page 

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