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ID

30079

Description

Diagnostic Benefits of HyperQTM vs. Conventional ECG Stress Test. Comparison of HyperQ vs. Stress ECG in Women Before Angiography; ODM derived from: https://clinicaltrials.gov/show/NCT00850486

Lien

https://clinicaltrials.gov/show/NCT00850486

Mots-clés

Versions (2)
  1. 08/05/2018 08/05/2018 -
  2. 08/05/2018 08/05/2018 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

8 mai 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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    Eligibility Ischemic Heart Disease NCT00850486

    Anglais

    Eligibility Ischemic Heart Disease NCT00850486

    1 Formulaires  
    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    a woman who was referred to angiography.
    Description

    Gender | Referral to Angiography

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0079399
    UMLS CUI [2,1]
    C2585021
    UMLS CUI [2,2]
    C0002978
    a woman who is able (i.e. no contraindications) to perform an exercise stress test
    Description

    Gender | Exercise test Ability

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0079399
    UMLS CUI [2,1]
    C0015260
    UMLS CUI [2,2]
    C0085732
    a woman who signed an informed consent form.
    Description

    Gender | Informed Consent

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0079399
    UMLS CUI [2]
    C0021430
    Exclusion Criteria
    Description

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    contraindications for an exercise test
    Description

    Medical contraindication Exercise test

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C1301624
    UMLS CUI [1,2]
    C0015260
    wolff-parkinson-white (pre-excitation) syndrome.
    Description

    Wolff-Parkinson-White Syndrome | Preexcitation

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0043202
    UMLS CUI [2]
    C0032915
    left bundle branch block, complete right bundle branch block or qrs duration > 120 ms, change in qrs morphology during exercise
    Description

    Left Bundle-Branch Block | Complete right bundle branch block | QRS complex duration | QRS complex Change During Exercise

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0023211
    UMLS CUI [2]
    C0344422
    UMLS CUI [3]
    C0429025
    UMLS CUI [4,1]
    C0429097
    UMLS CUI [4,2]
    C0392747
    UMLS CUI [4,3]
    C0347984
    UMLS CUI [4,4]
    C0015259
    atrial fibrillation or significant ventricular arrhythmia
    Description

    Atrial Fibrillation | Ventricular arrhythmia

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0004238
    UMLS CUI [2]
    C0085612
    treatment with digoxin
    Description

    Digoxin

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0012265
    pacemaker
    Description

    Artificial cardiac pacemaker

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0030163
    having taken beta blockers within 24 hours before the exercise test
    Description

    Adrenergic beta-1 Receptor Antagonists Before Exercise test

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0304516
    UMLS CUI [1,2]
    C0332152
    UMLS CUI [1,3]
    C0015260
    pregnancy or suspected pregnancy
    Description

    Pregnancy | Pregnancy Suspected

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0032961
    UMLS CUI [2,1]
    C0032961
    UMLS CUI [2,2]
    C0750491
    Retour au début de la page

    Similar models

    Eligibility Ischemic Heart Disease NCT00850486

    1 Formulaires
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Gender | Referral to Angiography
    Item
    a woman who was referred to angiography.
    boolean
    C0079399 (UMLS CUI [1])
    C2585021 (UMLS CUI [2,1])
    C0002978 (UMLS CUI [2,2])
    Gender | Exercise test Ability
    Item
    a woman who is able (i.e. no contraindications) to perform an exercise stress test
    boolean
    C0079399 (UMLS CUI [1])
    C0015260 (UMLS CUI [2,1])
    C0085732 (UMLS CUI [2,2])
    Gender | Informed Consent
    Item
    a woman who signed an informed consent form.
    boolean
    C0079399 (UMLS CUI [1])
    C0021430 (UMLS CUI [2])
    Item Group
    C0680251 (UMLS CUI)
    Medical contraindication Exercise test
    Item
    contraindications for an exercise test
    boolean
    C1301624 (UMLS CUI [1,1])
    C0015260 (UMLS CUI [1,2])
    Wolff-Parkinson-White Syndrome | Preexcitation
    Item
    wolff-parkinson-white (pre-excitation) syndrome.
    boolean
    C0043202 (UMLS CUI [1])
    C0032915 (UMLS CUI [2])
    Left Bundle-Branch Block | Complete right bundle branch block | QRS complex duration | QRS complex Change During Exercise
    Item
    left bundle branch block, complete right bundle branch block or qrs duration > 120 ms, change in qrs morphology during exercise
    boolean
    C0023211 (UMLS CUI [1])
    C0344422 (UMLS CUI [2])
    C0429025 (UMLS CUI [3])
    C0429097 (UMLS CUI [4,1])
    C0392747 (UMLS CUI [4,2])
    C0347984 (UMLS CUI [4,3])
    C0015259 (UMLS CUI [4,4])
    Atrial Fibrillation | Ventricular arrhythmia
    Item
    atrial fibrillation or significant ventricular arrhythmia
    boolean
    C0004238 (UMLS CUI [1])
    C0085612 (UMLS CUI [2])
    Digoxin
    Item
    treatment with digoxin
    boolean
    C0012265 (UMLS CUI [1])
    Artificial cardiac pacemaker
    Item
    pacemaker
    boolean
    C0030163 (UMLS CUI [1])
    Adrenergic beta-1 Receptor Antagonists Before Exercise test
    Item
    having taken beta blockers within 24 hours before the exercise test
    boolean
    C0304516 (UMLS CUI [1,1])
    C0332152 (UMLS CUI [1,2])
    C0015260 (UMLS CUI [1,3])
    Pregnancy | Pregnancy Suspected
    Item
    pregnancy or suspected pregnancy
    boolean
    C0032961 (UMLS CUI [1])
    C0032961 (UMLS CUI [2,1])
    C0750491 (UMLS CUI [2,2])
    Retour au début de la page 

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