ID

39964

Beschreibung

Comparison of Effect of cARvedilol Compared To bISoprolol on cenTral Pulse Pressure in Hypertension (ARTIST) Study; ODM derived from: https://clinicaltrials.gov/show/NCT01243827

Link

https://clinicaltrials.gov/show/NCT01243827

Stichworte

Versionen (1)
  1. 06.03.20 06.03.20 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

6. März 2020

DOI

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Creative Commons BY 4.0
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Eligibility Hypertension NCT01243827

Englisch

Eligibility Hypertension NCT01243827

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
never-treated hypertensive subjects, aged 20-80 years (at the time of informed consent), regardless of sex
Beschreibung

Hypertensive disease Untreated | Age

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C0332155
UMLS CUI [2]
C0001779
clinic systolic bp/diastolic bp > 140/90 mmhg in a sitting position.
Beschreibung

Sitting systolic blood pressure | Sitting diastolic blood pressure

Datentyp

boolean

Alias
UMLS CUI [1]
C1319893
UMLS CUI [2]
C1319894
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
beta−blocker contraindications(asthma, copd…)
Beschreibung

Medical contraindication Adrenergic beta-1 Receptor Antagonists | Asthma | Chronic Obstructive Airway Disease

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0304516
UMLS CUI [2]
C0004096
UMLS CUI [3]
C0024117
heart rate less than 55 bpm
Beschreibung

Heart rate

Datentyp

boolean

Alias
UMLS CUI [1]
C0018810
subjects treated with nitrates
Beschreibung

Nitrates

Datentyp

boolean

Alias
UMLS CUI [1]
C0028125
grade 3 hypertension (≥180 and/or ≥110 mmhg)
Beschreibung

Hypertensive disease Grade | Blood pressure determination

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C0441800
UMLS CUI [2]
C0005824
secondary hypertension or malignant hypertension
Beschreibung

Secondary hypertension | Malignant Hypertension

Datentyp

boolean

Alias
UMLS CUI [1]
C0155616
UMLS CUI [2]
C0020540
history of heart failure, coronary artery disease, and stroke
Beschreibung

Heart failure | Coronary Artery Disease | Cerebrovascular accident

Datentyp

boolean

Alias
UMLS CUI [1]
C0018801
UMLS CUI [2]
C1956346
UMLS CUI [3]
C0038454
arrhythmia
Beschreibung

Cardiac Arrhythmia

Datentyp

boolean

Alias
UMLS CUI [1]
C0003811
renal dysfunction (serum creatinine ≥2.0 mg/dl)
Beschreibung

Renal dysfunction | Creatinine measurement, serum

Datentyp

boolean

Alias
UMLS CUI [1]
C3279454
UMLS CUI [2]
C0201976
hepatic dysfunction (ast and/or alt ≥100 iu/l)
Beschreibung

Liver Dysfunction | Aspartate aminotransferase measurement | Alanine aminotransferase measurement

Datentyp

boolean

Alias
UMLS CUI [1]
C0086565
UMLS CUI [2]
C0201899
UMLS CUI [3]
C0201836
a history of or a suspected malignant tumor within 5 years of enrollment
Beschreibung

Malignant Neoplasms | Suspected malignancy

Datentyp

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2]
C0581833
chronic inflammatory disease
Beschreibung

Chronic inflammatory disorder

Datentyp

boolean

Alias
UMLS CUI [1]
C1290886
pregnancy, childbearing potential with inadequate contraception, breast feeding
Beschreibung

Pregnancy | Childbearing Potential Contraceptive methods Inadequate | Breast Feeding

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2,1]
C3831118
UMLS CUI [2,2]
C0700589
UMLS CUI [2,3]
C0205412
UMLS CUI [3]
C0006147
inability to give informed consent
Beschreibung

Informed Consent Unable

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
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Ähnliche Modelle

Eligibility Hypertension NCT01243827

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Hypertensive disease Untreated | Age
Item
never-treated hypertensive subjects, aged 20-80 years (at the time of informed consent), regardless of sex
boolean
C0020538 (UMLS CUI [1,1])
C0332155 (UMLS CUI [1,2])
C0001779 (UMLS CUI [2])
Sitting systolic blood pressure | Sitting diastolic blood pressure
Item
clinic systolic bp/diastolic bp > 140/90 mmhg in a sitting position.
boolean
C1319893 (UMLS CUI [1])
C1319894 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Medical contraindication Adrenergic beta-1 Receptor Antagonists | Asthma | Chronic Obstructive Airway Disease
Item
beta−blocker contraindications(asthma, copd…)
boolean
C1301624 (UMLS CUI [1,1])
C0304516 (UMLS CUI [1,2])
C0004096 (UMLS CUI [2])
C0024117 (UMLS CUI [3])
Heart rate
Item
heart rate less than 55 bpm
boolean
C0018810 (UMLS CUI [1])
Nitrates
Item
subjects treated with nitrates
boolean
C0028125 (UMLS CUI [1])
Hypertensive disease Grade | Blood pressure determination
Item
grade 3 hypertension (≥180 and/or ≥110 mmhg)
boolean
C0020538 (UMLS CUI [1,1])
C0441800 (UMLS CUI [1,2])
C0005824 (UMLS CUI [2])
Secondary hypertension | Malignant Hypertension
Item
secondary hypertension or malignant hypertension
boolean
C0155616 (UMLS CUI [1])
C0020540 (UMLS CUI [2])
Heart failure | Coronary Artery Disease | Cerebrovascular accident
Item
history of heart failure, coronary artery disease, and stroke
boolean
C0018801 (UMLS CUI [1])
C1956346 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
Cardiac Arrhythmia
Item
arrhythmia
boolean
C0003811 (UMLS CUI [1])
Renal dysfunction | Creatinine measurement, serum
Item
renal dysfunction (serum creatinine ≥2.0 mg/dl)
boolean
C3279454 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
Liver Dysfunction | Aspartate aminotransferase measurement | Alanine aminotransferase measurement
Item
hepatic dysfunction (ast and/or alt ≥100 iu/l)
boolean
C0086565 (UMLS CUI [1])
C0201899 (UMLS CUI [2])
C0201836 (UMLS CUI [3])
Malignant Neoplasms | Suspected malignancy
Item
a history of or a suspected malignant tumor within 5 years of enrollment
boolean
C0006826 (UMLS CUI [1])
C0581833 (UMLS CUI [2])
Chronic inflammatory disorder
Item
chronic inflammatory disease
boolean
C1290886 (UMLS CUI [1])
Pregnancy | Childbearing Potential Contraceptive methods Inadequate | Breast Feeding
Item
pregnancy, childbearing potential with inadequate contraception, breast feeding
boolean
C0032961 (UMLS CUI [1])
C3831118 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
C0205412 (UMLS CUI [2,3])
C0006147 (UMLS CUI [3])
Informed Consent Unable
Item
inability to give informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
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