Informations:
Erreur:
ID
33826
Description
A Clinical Study With Aliskiren Alone or in Combination Therapy With Diuretic Hctz in Venezuelan Hypertensive Patients.; ODM derived from: https://clinicaltrials.gov/show/NCT01056731
Lien
https://clinicaltrials.gov/show/NCT01056731
Mots-clés
Versions (1)
- 02/01/2019 02/01/2019 -
Détendeur de droits
See clinicaltrials.gov
Téléchargé le
2 janvier 2019
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
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Eligibility High Blood Pressure NCT01056731
Eligibility High Blood Pressure NCT01056731
- StudyEvent: Eligibility
Similar models
Eligibility High Blood Pressure NCT01056731
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Outpatients | Essential Hypertension Stage | Therapy naive | Essential Hypertension Uncontrolled
Item
outpatients, with essential hypertension, stage i-ii, naïve or not controlled with monotherapy.
boolean
C0029921 (UMLS CUI [1])
C0085580 (UMLS CUI [2,1])
C1306673 (UMLS CUI [2,2])
C0919936 (UMLS CUI [3])
C0085580 (UMLS CUI [4,1])
C0205318 (UMLS CUI [4,2])
C0085580 (UMLS CUI [2,1])
C1306673 (UMLS CUI [2,2])
C0919936 (UMLS CUI [3])
C0085580 (UMLS CUI [4,1])
C0205318 (UMLS CUI [4,2])
Blood pressure determination
Item
bp> 180/110 mmhg
boolean
C0005824 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnant or nursing women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Hypertensive Encephalopathy | Cerebrovascular accident | Transient Ischemic Attack
Item
hypertensive encephalopathy or cerebrovascular accident, transient ischemic -
boolean
C0151620 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
C0007787 (UMLS CUI [3])
C0038454 (UMLS CUI [2])
C0007787 (UMLS CUI [3])
Myocardial Infarction | Angina, Unstable | Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention
Item
cerebral attack, myocardial infarction, unstable angina, coronary bypass surgery, percutaneous coronary intervention within 6 month
boolean
C0027051 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
C0010055 (UMLS CUI [3])
C1532338 (UMLS CUI [4])
C0002965 (UMLS CUI [2])
C0010055 (UMLS CUI [3])
C1532338 (UMLS CUI [4])
Potassium measurement
Item
k <3.5 meq/l or ≥ 5 meq/l
boolean
C0202194 (UMLS CUI [1])
Renal Insufficiency
Item
renal impairment
boolean
C1565489 (UMLS CUI [1])
Hydrochlorothiazide allergy | Hypersensitivity Aliskiren | Angioedema Due to Angiotensin-Converting Enzyme Inhibitors | Angioedema Due to Angiotensin II receptor antagonist
Item
hypersensitivity to hctz or aliskiren or angioedema due to ace-i or arb
boolean
C0571898 (UMLS CUI [1])
C0020517 (UMLS CUI [2,1])
C1120110 (UMLS CUI [2,2])
C0002994 (UMLS CUI [3,1])
C0678226 (UMLS CUI [3,2])
C0003015 (UMLS CUI [3,3])
C0002994 (UMLS CUI [4,1])
C0678226 (UMLS CUI [4,2])
C0521942 (UMLS CUI [4,3])
C0020517 (UMLS CUI [2,1])
C1120110 (UMLS CUI [2,2])
C0002994 (UMLS CUI [3,1])
C0678226 (UMLS CUI [3,2])
C0003015 (UMLS CUI [3,3])
C0002994 (UMLS CUI [4,1])
C0678226 (UMLS CUI [4,2])
C0521942 (UMLS CUI [4,3])
Eligibility Criteria Study Protocol
Item
other protocol-defined inclusion/exclusion criteria may apply
boolean
C1516637 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C2348563 (UMLS CUI [1,2])