ID

20792

Beschrijving

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

Trefwoorden

Versies (1)
  1. 18-03-17 18-03-17 -
Geüploaded op

18 maart 2017

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Essential Hypertension NCT00380289

Engels

Eligibility Essential Hypertension NCT00380289

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

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

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
hypertension- either
Beschrijving

Hypertensive disease

Datatype

boolean

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

Hypertensive disease untreated | Blood Pressure

Datatype

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
Beschrijving

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

Datatype

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.
Beschrijving

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

Datatype

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
Beschrijving

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.
Beschrijving

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

Datatype

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.
Beschrijving

Intolerance to Pharmaceutical Preparations

Datatype

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.
Beschrijving

Gout | Asthma | Medical contraindication Investigational New Drugs

Datatype

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.
Beschrijving

Childbearing Potential Contraceptive methods Missing

Datatype

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)
Beschrijving

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

Datatype

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
Beschrijving

Informed Consent Unable

Datatype

boolean

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

Diabetes Mellitus

Datatype

boolean

Alias
UMLS CUI [1]
C0011849
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Similar models

Eligibility Essential Hypertension NCT00380289

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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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