ID

43403

Description

ODM derived from http://clinicaltrials.gov/show/NCT00680550

Lien

http://clinicaltrials.gov/show/NCT00680550

Mots-clés

Versions (3)
  1. 09/12/2013 09/12/2013 - Martin Dugas
  2. 15/04/2014 15/04/2014 - Julian Varghese
  3. 20/09/2021 20/09/2021 -
Téléchargé le

20 septembre 2021

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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    Eligibility NCT00680550 Atrial Fibrillation

    Allemand Anglais

    Eligibility

    1 Formulaires  
    1. StudyEvent: Eligibility
      1. Eligibility
    Einschlusskriterien
    Description

    Einschlusskriterien

    Alias
    UMLS CUI 2011AA
    CL425202
    Alter mindestens 18 Jahre
    Description

    age at least 18 Years

    Type de données

    boolean

    Alias
    UMLS CUI 2011AA
    C0001779
    SNOMED CT 2011_0131
    397669002
    Patient implanted or scheduled for an implant with a Reveal XT Insertable Cardiac Monitor System for arrhythmia diagnosis or monitoring
    Description

    Patient implanted or scheduled for an implant with a Reveal XT Insertable Cardiac Monitor System for arrhythmia diagnosis or monitoring

    Type de données

    boolean

    Alias
    UMLS CUI 2011AA
    C0021102
    SNOMED CT 2011_0131
    40388003
    UMLS CUI 2011AA
    C0086960
    UMLS CUI 2011AA
    C1883719
    UMLS CUI 2011AA
    C0179608
    UMLS CUI 2011AA
    C0150496
    SNOMED CT 2011_0131
    23852006
    MedDRA 14.1
    10053438
    UMLS CUI 2011AA
    C0003811
    SNOMED CT 2011_0131
    44808001
    MedDRA 14.1
    10003119
    ICD-9-CM Version 2011
    427.9
    UMLS CUI 2011AA
    C0011900
    SNOMED CT 2011_0131
    439401001
    LOINC Version 232
    MTHU008876
    UMLS CUI 2011AA
    CL415337
    Patient must be willing to sign a Patient Data Release Form (or Informed Consent where applicable)
    Description

    Patient must be willing to sign a Patient Data Release Form (or Informed Consent where applicable)

    Type de données

    boolean

    Alias
    UMLS CUI 2011AA
    C0021430
    Ausschlusskriterien
    Description

    Ausschlusskriterien

    Alias
    UMLS CUI 2011AA
    CL425201
    Enrollment outside a 30-day window from the planned/performed Reveal XT implant procedure (from 15 days pre-implant until 15 days post implant)
    Description

    Enrollment outside a 30-day window from the planned/performed Reveal XT implant procedure (from 15 days pre-implant until 15 days post implant)

    Type de données

    boolean

    Alias
    UMLS CUI 2011AA
    C1516879
    UMLS CUI 2011AA
    CL411789
    UMLS CUI 2011AA
    C0439231
    SNOMED CT 2011_0131
    258706009
    HL7 V3 2006_05
    MO
    UMLS CUI 2011AA
    C0040223
    SNOMED CT 2011_0131
    410670007
    LOINC Version 232
    MTHU009151
    UMLS CUI 2011AA
    C1301732
    SNOMED CT 2011_0131
    397943006
    UMLS CUI 2011AA
    C0884358
    SNOMED CT 2011_0131
    398166005
    UMLS CUI 2011AA
    C0021107
    SNOMED CT 2011_0131
    71861002
    LOINC Version 232
    MTHU035917
    UMLS CUI 2011AA
    C2825407
    UMLS CUI 2011AA
    C0439231
    SNOMED CT 2011_0131
    258706009
    HL7 V3 2006_05
    MO
    UMLS CUI 2011AA
    C0332152
    SNOMED CT 2011_0131
    288556008
    UMLS CUI 2011AA
    C0021102
    SNOMED CT 2011_0131
    40388003
    UMLS CUI 2011AA
    C2825407
    UMLS CUI 2011AA
    C0439231
    SNOMED CT 2011_0131
    258706009
    HL7 V3 2006_05
    MO
    UMLS CUI 2011AA
    C0231290
    SNOMED CT 2011_0131
    237679004
    UMLS CUI 2011AA
    C0021102
    SNOMED CT 2011_0131
    40388003
    Patient is implanted with a pacemaker, ICD, CRT-device or an implantable hemodynamic monitoring system
    Description

    Patient is implanted with a pacemaker, ICD, CRT-device or an implantable hemodynamic monitoring system

    Type de données

    boolean

    Alias
    UMLS CUI 2011AA
    C0021102
    SNOMED CT 2011_0131
    40388003
    UMLS CUI 2011AA
    C0030163
    SNOMED CT 2011_0131
    14106009
    LOINC Version 232
    MTHU024521
    UMLS CUI 2011AA
    C0162589
    SNOMED CT 2011_0131
    72506001
    UMLS CUI 2011AA
    C2936377
    UMLS CUI 2011AA
    C0021102
    SNOMED CT 2011_0131
    40388003
    UMLS CUI 2011AA
    C0161959
    SNOMED CT 2011_0131
    48428001
    ICD-9-CM Version 2011
    89.6
    Unwillingness or inability to cooperate or give written informed consent or, if the patient is a minor and the legal guardian refuses to give consent
    Description

    Unwillingness or inability to cooperate or give written informed consent or, if the patient is a minor and the legal guardian refuses to give consent

    Type de données

    boolean

    Alias
    UMLS CUI 2011AA
    C0558080
    SNOMED CT 2011_0131
    225465005
    UMLS CUI 2011AA
    C1299582
    SNOMED CT 2011_0131
    371151008
    UMLS CUI 2011AA
    C0392337
    UMLS CUI 2011AA
    C1576874
    HL7 V3 2006_05
    WRITTEN
    UMLS CUI 2011AA
    C0021430
    UMLS CUI 2011AA
    C0750557
    UMLS CUI 2011AA
    C0026193
    SNOMED CT 2011_0131
    410599005
    UMLS CUI 2011AA
    C0023226
    SNOMED CT 2011_0131
    58626002
    LOINC Version 232
    MTHU020628
    UMLS CUI 2011AA
    C1705116
    SNOMED CT 2011_0131
    443390004
    UMLS CUI 2011AA
    C1511481
    LOINC Version 232
    MTHU035862
    Retour au début de la page

    Similar models

    Eligibility

    1 Formulaires
    1. StudyEvent: Eligibility
      1. Eligibility
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    Einschlusskriterien
    CL425202 (UMLS CUI 2011AA)
    age at least 18 Years
    Item
    Alter mindestens 18 Jahre
    boolean
    C0001779 (UMLS CUI 2011AA)
    397669002 (SNOMED CT 2011_0131)
    Patient implanted or scheduled for an implant with a Reveal XT Insertable Cardiac Monitor System for arrhythmia diagnosis or monitoring
    Item
    Patient implanted or scheduled for an implant with a Reveal XT Insertable Cardiac Monitor System for arrhythmia diagnosis or monitoring
    boolean
    C0021102 (UMLS CUI 2011AA)
    40388003 (SNOMED CT 2011_0131)
    C0086960 (UMLS CUI 2011AA)
    C1883719 (UMLS CUI 2011AA)
    C0179608 (UMLS CUI 2011AA)
    C0150496 (UMLS CUI 2011AA)
    23852006 (SNOMED CT 2011_0131)
    10053438 (MedDRA 14.1)
    C0003811 (UMLS CUI 2011AA)
    44808001 (SNOMED CT 2011_0131)
    10003119 (MedDRA 14.1)
    427.9 (ICD-9-CM Version 2011)
    C0011900 (UMLS CUI 2011AA)
    439401001 (SNOMED CT 2011_0131)
    MTHU008876 (LOINC Version 232)
    CL415337 (UMLS CUI 2011AA)
    Patient must be willing to sign a Patient Data Release Form (or Informed Consent where applicable)
    Item
    Patient must be willing to sign a Patient Data Release Form (or Informed Consent where applicable)
    boolean
    C0021430 (UMLS CUI 2011AA)
    Item Group
    Ausschlusskriterien
    CL425201 (UMLS CUI 2011AA)
    Enrollment outside a 30-day window from the planned/performed Reveal XT implant procedure (from 15 days pre-implant until 15 days post implant)
    Item
    Enrollment outside a 30-day window from the planned/performed Reveal XT implant procedure (from 15 days pre-implant until 15 days post implant)
    boolean
    C1516879 (UMLS CUI 2011AA)
    CL411789 (UMLS CUI 2011AA)
    C0439231 (UMLS CUI 2011AA)
    258706009 (SNOMED CT 2011_0131)
    MO (HL7 V3 2006_05)
    C0040223 (UMLS CUI 2011AA)
    410670007 (SNOMED CT 2011_0131)
    MTHU009151 (LOINC Version 232)
    C1301732 (UMLS CUI 2011AA)
    397943006 (SNOMED CT 2011_0131)
    C0884358 (UMLS CUI 2011AA)
    398166005 (SNOMED CT 2011_0131)
    C0021107 (UMLS CUI 2011AA)
    71861002 (SNOMED CT 2011_0131)
    MTHU035917 (LOINC Version 232)
    C2825407 (UMLS CUI 2011AA)
    C0439231 (UMLS CUI 2011AA)
    258706009 (SNOMED CT 2011_0131)
    MO (HL7 V3 2006_05)
    C0332152 (UMLS CUI 2011AA)
    288556008 (SNOMED CT 2011_0131)
    C0021102 (UMLS CUI 2011AA)
    40388003 (SNOMED CT 2011_0131)
    C2825407 (UMLS CUI 2011AA)
    C0439231 (UMLS CUI 2011AA)
    258706009 (SNOMED CT 2011_0131)
    MO (HL7 V3 2006_05)
    C0231290 (UMLS CUI 2011AA)
    237679004 (SNOMED CT 2011_0131)
    C0021102 (UMLS CUI 2011AA)
    40388003 (SNOMED CT 2011_0131)
    Patient is implanted with a pacemaker, ICD, CRT-device or an implantable hemodynamic monitoring system
    Item
    Patient is implanted with a pacemaker, ICD, CRT-device or an implantable hemodynamic monitoring system
    boolean
    C0021102 (UMLS CUI 2011AA)
    40388003 (SNOMED CT 2011_0131)
    C0030163 (UMLS CUI 2011AA)
    14106009 (SNOMED CT 2011_0131)
    MTHU024521 (LOINC Version 232)
    C0162589 (UMLS CUI 2011AA)
    72506001 (SNOMED CT 2011_0131)
    C2936377 (UMLS CUI 2011AA)
    C0021102 (UMLS CUI 2011AA)
    40388003 (SNOMED CT 2011_0131)
    C0161959 (UMLS CUI 2011AA)
    48428001 (SNOMED CT 2011_0131)
    89.6 (ICD-9-CM Version 2011)
    Unwillingness or inability to cooperate or give written informed consent or, if the patient is a minor and the legal guardian refuses to give consent
    Item
    Unwillingness or inability to cooperate or give written informed consent or, if the patient is a minor and the legal guardian refuses to give consent
    boolean
    C0558080 (UMLS CUI 2011AA)
    225465005 (SNOMED CT 2011_0131)
    C1299582 (UMLS CUI 2011AA)
    371151008 (SNOMED CT 2011_0131)
    C0392337 (UMLS CUI 2011AA)
    C1576874 (UMLS CUI 2011AA)
    WRITTEN (HL7 V3 2006_05)
    C0021430 (UMLS CUI 2011AA)
    C0750557 (UMLS CUI 2011AA)
    C0026193 (UMLS CUI 2011AA)
    410599005 (SNOMED CT 2011_0131)
    C0023226 (UMLS CUI 2011AA)
    58626002 (SNOMED CT 2011_0131)
    MTHU020628 (LOINC Version 232)
    C1705116 (UMLS CUI 2011AA)
    443390004 (SNOMED CT 2011_0131)
    C1511481 (UMLS CUI 2011AA)
    MTHU035862 (LOINC Version 232)
    Retour au début de la page 

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