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ID

15299

Beschreibung

Pharmacotherapy in Depression With Panic Spectrum; ODM derived from: https://clinicaltrials.gov/show/NCT00177996

Link

https://clinicaltrials.gov/show/NCT00177996

Stichworte

  1. 25/05/2016 25/05/2016 -
  2. 25/05/2016 25/05/2016 -
Hochgeladen am

25 mai 2016

DOI

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Lizenz

Creative Commons BY 4.0

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    Eligibility Major Depression NCT00177996

    Eligibility Major Depression NCT00177996

    Inclusion Criteria
    Beschreibung

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    male or female ages 18-60;
    Beschreibung

    age

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    current diagnosis of major depression, and a rating of ³15 on the hrs-d-25; --presence of significant, co-existing panic-agoraphobic spectrum symptoms,
    Beschreibung

    major depression

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C1269683
    absence of ongoing therapy with psychotropic medications (except for intermittent use of nonbenzodiazepine hypnotics) or willingness to be withdrawn from an ineffective ongoing antidepressant medications
    Beschreibung

    therapy with psychotropic medications

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0033978
    physically healthy,
    Beschreibung

    physically healthy

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0018759
    female participants of childbearing potential must be practicing a medically acceptable form of double-barrier birth control or using oral contraceptives such as birth control pills, implants, or injections;
    Beschreibung

    contraceptive use

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C1999124
    Exclusion Criteria
    Beschreibung

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    females who are pregnant or breast-feeding;
    Beschreibung

    pregnant or breast-feeding

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0032961
    UMLS CUI [1,2]
    C0006147
    history of suicide attempt in the 6 months prior to entry, active suicidal ideation, or significant suicide risk;
    Beschreibung

    history of suicide attempt

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0038663
    UMLS CUI [2]
    C0438696
    history of hypersensitivity to or current use of sertraline;
    Beschreibung

    history of hypersensitivity

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0020517
    UMLS CUI [2]
    C0074393
    unstable or untreated medical conditions,
    Beschreibung

    untreated medical conditions

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0009488
    participants who do not wish to discontinue current, ineffective antidepressant treatment;
    Beschreibung

    discontinue antidepressant treatment

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0003289
    UMLS CUI [1,2]
    C1518544
    participants who have recently begun psychotherapy (less than 3 months prior to study entry);
    Beschreibung

    psychotherapy

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0033968
    diagnosis of current panic disorder, psychosis, substance or alcohol abuse, anorexia, bulimia, dissociative, bipolar disorder, or any other psychiatric or medical illness that would interfere with the best treatment strategy for the potential participant.
    Beschreibung

    exclusion diagnoses

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0030319
    UMLS CUI [2]
    C0033975
    UMLS CUI [3]
    C0038586
    UMLS CUI [4]
    C0003123
    UMLS CUI [5]
    C0006370
    UMLS CUI [6]
    C0005586

    Ähnliche Modelle

    Eligibility Major Depression NCT00177996

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    Alias
    Item Group
    C1512693 (UMLS CUI)
    age
    Item
    male or female ages 18-60;
    boolean
    C0001779 (UMLS CUI [1])
    major depression
    Item
    current diagnosis of major depression, and a rating of ³15 on the hrs-d-25; --presence of significant, co-existing panic-agoraphobic spectrum symptoms,
    boolean
    C1269683 (UMLS CUI [1])
    therapy with psychotropic medications
    Item
    absence of ongoing therapy with psychotropic medications (except for intermittent use of nonbenzodiazepine hypnotics) or willingness to be withdrawn from an ineffective ongoing antidepressant medications
    boolean
    C0033978 (UMLS CUI [1])
    physically healthy
    Item
    physically healthy,
    boolean
    C0018759 (UMLS CUI [1])
    contraceptive use
    Item
    female participants of childbearing potential must be practicing a medically acceptable form of double-barrier birth control or using oral contraceptives such as birth control pills, implants, or injections;
    boolean
    C1999124 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    pregnant or breast-feeding
    Item
    females who are pregnant or breast-feeding;
    boolean
    C0032961 (UMLS CUI [1,1])
    C0006147 (UMLS CUI [1,2])
    history of suicide attempt
    Item
    history of suicide attempt in the 6 months prior to entry, active suicidal ideation, or significant suicide risk;
    boolean
    C0038663 (UMLS CUI [1])
    C0438696 (UMLS CUI [2])
    history of hypersensitivity
    Item
    history of hypersensitivity to or current use of sertraline;
    boolean
    C0020517 (UMLS CUI [1])
    C0074393 (UMLS CUI [2])
    untreated medical conditions
    Item
    unstable or untreated medical conditions,
    boolean
    C0009488 (UMLS CUI [1])
    discontinue antidepressant treatment
    Item
    participants who do not wish to discontinue current, ineffective antidepressant treatment;
    boolean
    C0003289 (UMLS CUI [1,1])
    C1518544 (UMLS CUI [1,2])
    psychotherapy
    Item
    participants who have recently begun psychotherapy (less than 3 months prior to study entry);
    boolean
    C0033968 (UMLS CUI [1])
    exclusion diagnoses
    Item
    diagnosis of current panic disorder, psychosis, substance or alcohol abuse, anorexia, bulimia, dissociative, bipolar disorder, or any other psychiatric or medical illness that would interfere with the best treatment strategy for the potential participant.
    boolean
    C0030319 (UMLS CUI [1])
    C0033975 (UMLS CUI [2])
    C0038586 (UMLS CUI [3])
    C0003123 (UMLS CUI [4])
    C0006370 (UMLS CUI [5])
    C0005586 (UMLS CUI [6])

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