ID

16154

Beschreibung

To Evaluate the Impact of Oral Flecainide on Quality of Life in Patients With Paroxysmal Atrial Fibrillation; ODM derived from: https://clinicaltrials.gov/show/NCT00189319

Link

https://clinicaltrials.gov/show/NCT00189319

Stichworte

  1. 02.07.16 02.07.16 -
  2. 02.07.16 02.07.16 -
Hochgeladen am

2. Juli 2016

DOI

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Lizenz

Creative Commons BY 4.0

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    Eligibility Atrial Fibrillation NCT00189319

    Eligibility Atrial Fibrillation NCT00189319

    Inclusion Criteria
    Beschreibung

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    in sinus rhythm at treatment initiation
    Beschreibung

    Sinus rhythm During Therapeutic procedure Initiation

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0232201
    UMLS CUI [1,2]
    C0347984
    UMLS CUI [1,3]
    C0087111
    UMLS CUI [1,4]
    C1704686
    experienced symptomatic af episodes
    Beschreibung

    Atrial Fibrillation Episode Symptomatic

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0004238
    UMLS CUI [1,2]
    C0332189
    UMLS CUI [1,3]
    C0231220
    left ventricular ejection fraction of at least 40%
    Beschreibung

    Left ventricular ejection fraction

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0428772
    females of child bearing potential must be using reliable method of contraception
    Beschreibung

    Childbearing Potential Contraceptive methods

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C3831118
    UMLS CUI [1,2]
    C0700589
    Exclusion Criteria
    Beschreibung

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    intolerance and/or failure of previous therapy with flecainide immediate release
    Beschreibung

    intolerance to Flecainide Immediate Release | Flecainide Immediate Release Prior Therapy failed

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C1744706
    UMLS CUI [1,2]
    C0016229
    UMLS CUI [1,3]
    C1708470
    UMLS CUI [2,1]
    C0016229
    UMLS CUI [2,2]
    C1708470
    UMLS CUI [2,3]
    C1514463
    UMLS CUI [2,4]
    C0231175
    currently receiving >200mg/day flecainide immediate release
    Beschreibung

    Flecainide Immediate Release Daily Dose

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0016229
    UMLS CUI [1,2]
    C1708470
    UMLS CUI [1,3]
    C2348070
    severe symptoms during episodes of arrhythmia
    Beschreibung

    Symptom severe During Cardiac Arrhythmia Episode

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0436345
    UMLS CUI [1,2]
    C0347984
    UMLS CUI [1,3]
    C0003811
    UMLS CUI [1,4]
    C0332189
    history of other cardiac conditions/abnormalities
    Beschreibung

    Heart Diseases | Congenital Heart Defects

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0018799
    UMLS CUI [2]
    C0018798
    heart surgery within the last 2 months
    Beschreibung

    Cardiac Surgery procedures

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0018821
    renal failure
    Beschreibung

    Kidney Failure

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0035078
    pregnant or lactating females
    Beschreibung

    Pregnancy | Breast Feeding

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0032961
    UMLS CUI [2]
    C0006147
    significant extra cardiac or systemic disease
    Beschreibung

    Heart Diseases Significant Additional | Systemic disease Significant Additional

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0018799
    UMLS CUI [1,2]
    C0750502
    UMLS CUI [1,3]
    C1524062
    UMLS CUI [2,1]
    C0442893
    UMLS CUI [2,2]
    C0750502
    UMLS CUI [2,3]
    C1524062
    abnormal electrolyte levels
    Beschreibung

    Electrolytes abnormal

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0151613
    receiving defined cardiac and/or other treatments
    Beschreibung

    Heart Therapeutic procedure Defined | Therapeutic procedure

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0018787
    UMLS CUI [1,2]
    C0087111
    UMLS CUI [1,3]
    C1704788
    UMLS CUI [2]
    C0087111

    Ähnliche Modelle

    Eligibility Atrial Fibrillation NCT00189319

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Sinus rhythm During Therapeutic procedure Initiation
    Item
    in sinus rhythm at treatment initiation
    boolean
    C0232201 (UMLS CUI [1,1])
    C0347984 (UMLS CUI [1,2])
    C0087111 (UMLS CUI [1,3])
    C1704686 (UMLS CUI [1,4])
    Atrial Fibrillation Episode Symptomatic
    Item
    experienced symptomatic af episodes
    boolean
    C0004238 (UMLS CUI [1,1])
    C0332189 (UMLS CUI [1,2])
    C0231220 (UMLS CUI [1,3])
    Left ventricular ejection fraction
    Item
    left ventricular ejection fraction of at least 40%
    boolean
    C0428772 (UMLS CUI [1])
    Childbearing Potential Contraceptive methods
    Item
    females of child bearing potential must be using reliable method of contraception
    boolean
    C3831118 (UMLS CUI [1,1])
    C0700589 (UMLS CUI [1,2])
    Item Group
    C0680251 (UMLS CUI)
    intolerance to Flecainide Immediate Release | Flecainide Immediate Release Prior Therapy failed
    Item
    intolerance and/or failure of previous therapy with flecainide immediate release
    boolean
    C1744706 (UMLS CUI [1,1])
    C0016229 (UMLS CUI [1,2])
    C1708470 (UMLS CUI [1,3])
    C0016229 (UMLS CUI [2,1])
    C1708470 (UMLS CUI [2,2])
    C1514463 (UMLS CUI [2,3])
    C0231175 (UMLS CUI [2,4])
    Flecainide Immediate Release Daily Dose
    Item
    currently receiving >200mg/day flecainide immediate release
    boolean
    C0016229 (UMLS CUI [1,1])
    C1708470 (UMLS CUI [1,2])
    C2348070 (UMLS CUI [1,3])
    Symptom severe During Cardiac Arrhythmia Episode
    Item
    severe symptoms during episodes of arrhythmia
    boolean
    C0436345 (UMLS CUI [1,1])
    C0347984 (UMLS CUI [1,2])
    C0003811 (UMLS CUI [1,3])
    C0332189 (UMLS CUI [1,4])
    Heart Diseases | Congenital Heart Defects
    Item
    history of other cardiac conditions/abnormalities
    boolean
    C0018799 (UMLS CUI [1])
    C0018798 (UMLS CUI [2])
    Cardiac Surgery procedures
    Item
    heart surgery within the last 2 months
    boolean
    C0018821 (UMLS CUI [1])
    Kidney Failure
    Item
    renal failure
    boolean
    C0035078 (UMLS CUI [1])
    Pregnancy | Breast Feeding
    Item
    pregnant or lactating females
    boolean
    C0032961 (UMLS CUI [1])
    C0006147 (UMLS CUI [2])
    Heart Diseases Significant Additional | Systemic disease Significant Additional
    Item
    significant extra cardiac or systemic disease
    boolean
    C0018799 (UMLS CUI [1,1])
    C0750502 (UMLS CUI [1,2])
    C1524062 (UMLS CUI [1,3])
    C0442893 (UMLS CUI [2,1])
    C0750502 (UMLS CUI [2,2])
    C1524062 (UMLS CUI [2,3])
    Electrolytes abnormal
    Item
    abnormal electrolyte levels
    boolean
    C0151613 (UMLS CUI [1])
    Heart Therapeutic procedure Defined | Therapeutic procedure
    Item
    receiving defined cardiac and/or other treatments
    boolean
    C0018787 (UMLS CUI [1,1])
    C0087111 (UMLS CUI [1,2])
    C1704788 (UMLS CUI [1,3])
    C0087111 (UMLS CUI [2])

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