0 Avaliações
ID

20792

Descrição

Early Metabolic Changes With Thiazide or Beta Blocker Therapy for Essential Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT00380289

Link

https://clinicaltrials.gov/show/NCT00380289

Palavras-chave

Versões (1)
  1. 18/03/2017 18/03/2017 -
Transferido a

18 de março de 2017

DOI

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Licença

Creative Commons BY 4.0
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    Eligibility Essential Hypertension NCT00380289

    Inglês

    Eligibility Essential Hypertension NCT00380289

    1 Formulários  
    Inclusion Criteria
    Descrição

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    volunteers will be aged 18-75 years.
    Descrição

    Age

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    hypertension- either
    Descrição

    Hypertensive disease

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0020538
    untreated, bp 140-170/90-110
    Descrição

    Hypertensive disease untreated | Blood Pressure

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0020538
    UMLS CUI [1,2]
    C0332155
    UMLS CUI [2]
    C0005823
    treated for over 1 month with drugs other than beta blockers or diuretic and bp>140/85
    Descrição

    Hypertensive disease Treated | Adrenergic beta-1 Receptor Antagonists | Diuretics | Blood Pressure

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0020538
    UMLS CUI [1,2]
    C1522326
    UMLS CUI [2]
    C0304516
    UMLS CUI [3]
    C0012798
    UMLS CUI [4]
    C0005823
    treated for over 1 month with drugs other than beta blockers or diuretic and bp<140/85 and patient willing to change medication for eight months.
    Descrição

    Hypertensive disease Treated | Adrenergic beta-1 Receptor Antagonists | Diuretics | Blood Pressure | Change of medication Willing

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0020538
    UMLS CUI [1,2]
    C1522326
    UMLS CUI [2]
    C0304516
    UMLS CUI [3]
    C0012798
    UMLS CUI [4]
    C0005823
    UMLS CUI [5,1]
    C0580105
    UMLS CUI [5,2]
    C0600109
    Exclusion Criteria
    Descrição

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    any patient already taking thiazide diuretics or beta blockers in whom these drugs cannot be switched to alternative drugs with similar or better blood pressure control.
    Descrição

    Thiazide Diuretics | Adrenergic beta-1 Receptor Antagonists | Pharmaceutical Preparations Alternative | control of blood pressure Improvement Unsuccessful

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0012802
    UMLS CUI [2]
    C0304516
    UMLS CUI [3,1]
    C0013227
    UMLS CUI [3,2]
    C1523987
    UMLS CUI [4,1]
    C1753303
    UMLS CUI [4,2]
    C2986411
    UMLS CUI [4,3]
    C1272705
    any patient who is intolerant of these medications will be excluded from the study.
    Descrição

    Intolerance to Pharmaceutical Preparations

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C1744706
    UMLS CUI [1,2]
    C0013227
    patients with gout, asthma or any other contraindications to the study drugs will be excluded.
    Descrição

    Gout | Asthma | Medical contraindication Investigational New Drugs

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0018099
    UMLS CUI [2]
    C0004096
    UMLS CUI [3,1]
    C1301624
    UMLS CUI [3,2]
    C0013230
    women of child bearing age not using contraception.
    Descrição

    Childbearing Potential Contraceptive methods Missing

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C3831118
    UMLS CUI [1,2]
    C0700589
    UMLS CUI [1,3]
    C1705492
    volunteers with heart failure, liver failure, renal failure, terminal illnesses (e.g. cancer)
    Descrição

    Heart failure | Liver Failure | Kidney Failure | Terminal illness | Malignant Neoplasms

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0018801
    UMLS CUI [2]
    C0085605
    UMLS CUI [3]
    C0035078
    UMLS CUI [4]
    C0679247
    UMLS CUI [5]
    C0006826
    volunteers not able to give informed consent
    Descrição

    Informed Consent Unable

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0021430
    UMLS CUI [1,2]
    C1299582
    patients with diabetes
    Descrição

    Diabetes Mellitus

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0011849
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    Similar models

    Eligibility Essential Hypertension NCT00380289

    1 Formulários
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de dados
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Age
    Item
    volunteers will be aged 18-75 years.
    boolean
    C0001779 (UMLS CUI [1])
    Hypertensive disease
    Item
    hypertension- either
    boolean
    C0020538 (UMLS CUI [1])
    Hypertensive disease untreated | Blood Pressure
    Item
    untreated, bp 140-170/90-110
    boolean
    C0020538 (UMLS CUI [1,1])
    C0332155 (UMLS CUI [1,2])
    C0005823 (UMLS CUI [2])
    Hypertensive disease Treated | Adrenergic beta-1 Receptor Antagonists | Diuretics | Blood Pressure
    Item
    treated for over 1 month with drugs other than beta blockers or diuretic and bp>140/85
    boolean
    C0020538 (UMLS CUI [1,1])
    C1522326 (UMLS CUI [1,2])
    C0304516 (UMLS CUI [2])
    C0012798 (UMLS CUI [3])
    C0005823 (UMLS CUI [4])
    Hypertensive disease Treated | Adrenergic beta-1 Receptor Antagonists | Diuretics | Blood Pressure | Change of medication Willing
    Item
    treated for over 1 month with drugs other than beta blockers or diuretic and bp<140/85 and patient willing to change medication for eight months.
    boolean
    C0020538 (UMLS CUI [1,1])
    C1522326 (UMLS CUI [1,2])
    C0304516 (UMLS CUI [2])
    C0012798 (UMLS CUI [3])
    C0005823 (UMLS CUI [4])
    C0580105 (UMLS CUI [5,1])
    C0600109 (UMLS CUI [5,2])
    Item Group
    C0680251 (UMLS CUI)
    Thiazide Diuretics | Adrenergic beta-1 Receptor Antagonists | Pharmaceutical Preparations Alternative | control of blood pressure Improvement Unsuccessful
    Item
    any patient already taking thiazide diuretics or beta blockers in whom these drugs cannot be switched to alternative drugs with similar or better blood pressure control.
    boolean
    C0012802 (UMLS CUI [1])
    C0304516 (UMLS CUI [2])
    C0013227 (UMLS CUI [3,1])
    C1523987 (UMLS CUI [3,2])
    C1753303 (UMLS CUI [4,1])
    C2986411 (UMLS CUI [4,2])
    C1272705 (UMLS CUI [4,3])
    Intolerance to Pharmaceutical Preparations
    Item
    any patient who is intolerant of these medications will be excluded from the study.
    boolean
    C1744706 (UMLS CUI [1,1])
    C0013227 (UMLS CUI [1,2])
    Gout | Asthma | Medical contraindication Investigational New Drugs
    Item
    patients with gout, asthma or any other contraindications to the study drugs will be excluded.
    boolean
    C0018099 (UMLS CUI [1])
    C0004096 (UMLS CUI [2])
    C1301624 (UMLS CUI [3,1])
    C0013230 (UMLS CUI [3,2])
    Childbearing Potential Contraceptive methods Missing
    Item
    women of child bearing age not using contraception.
    boolean
    C3831118 (UMLS CUI [1,1])
    C0700589 (UMLS CUI [1,2])
    C1705492 (UMLS CUI [1,3])
    Heart failure | Liver Failure | Kidney Failure | Terminal illness | Malignant Neoplasms
    Item
    volunteers with heart failure, liver failure, renal failure, terminal illnesses (e.g. cancer)
    boolean
    C0018801 (UMLS CUI [1])
    C0085605 (UMLS CUI [2])
    C0035078 (UMLS CUI [3])
    C0679247 (UMLS CUI [4])
    C0006826 (UMLS CUI [5])
    Informed Consent Unable
    Item
    volunteers not able to give informed consent
    boolean
    C0021430 (UMLS CUI [1,1])
    C1299582 (UMLS CUI [1,2])
    Diabetes Mellitus
    Item
    patients with diabetes
    boolean
    C0011849 (UMLS CUI [1])
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