ID

30006

Beschrijving

Efficacy and Safety of Candesartan Cilexetil Plus Hydrochlorothiazide in Subjects With Severe Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT01012479

Link

https://clinicaltrials.gov/show/NCT01012479

Trefwoorden

Versies (1)
  1. 04-05-18 04-05-18 -
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See clinicaltrials.gov

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4 mei 2018

DOI

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Creative Commons BY 4.0
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Eligibility Hypertension NCT01012479

Engels

Eligibility Hypertension NCT01012479

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
confirmed diagnosis of essential hypertension.
Beschrijving

Essential Hypertension

Datatype

boolean

Alias
UMLS CUI [1]
C0085580
has systolic blood pressure between 150 mmhg and 200 mmhg and diastolic blood pressure between 110 mmhg and 120 mmhg.
Beschrijving

Systolic Pressure | Diastolic blood pressure

Datatype

boolean

Alias
UMLS CUI [1]
C0871470
UMLS CUI [2]
C0428883
has not received any antihypertensive treatment so far.
Beschrijving

Antihypertensive therapy Absent

Datatype

boolean

Alias
UMLS CUI [1,1]
C0585941
UMLS CUI [1,2]
C0332197
has a negative pregnancy test at baseline in females of childbearing potential. male and female participants with reproductive potential must use an approved contraceptive method during study treatment evaluation
Beschrijving

Childbearing Potential Pregnancy test negative | Females & males of reproductive potential Contraceptive methods

Datatype

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0427780
UMLS CUI [2,1]
C4034483
UMLS CUI [2,2]
C0700589
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
has a known or suspected secondary hypertension or primary hyperaldosteronism.
Beschrijving

Secondary hypertension | Conn Syndrome | Secondary hypertension Suspected | Conn Syndrome Suspected

Datatype

boolean

Alias
UMLS CUI [1]
C0155616
UMLS CUI [2]
C1384514
UMLS CUI [3,1]
C0155616
UMLS CUI [3,2]
C0750491
UMLS CUI [4,1]
C1384514
UMLS CUI [4,2]
C0750491
has impaired renal function.
Beschrijving

Renal Insufficiency

Datatype

boolean

Alias
UMLS CUI [1]
C1565489
has severe hepatic impairment.
Beschrijving

Hepatic impairment Severe

Datatype

boolean

Alias
UMLS CUI [1,1]
C0948807
UMLS CUI [1,2]
C0205082
has bilateral renal artery stenosis, solitary kidney or post-renal transplant status.
Beschrijving

Bilateral renal artery stenosis | Kidney Solitary | Status post Kidney Transplantation

Datatype

boolean

Alias
UMLS CUI [1]
C0856760
UMLS CUI [2,1]
C0022646
UMLS CUI [2,2]
C0205171
UMLS CUI [3,1]
C0231290
UMLS CUI [3,2]
C0022671
has a history of myocardial infarction, coronary artery bypass graft, percutaneous coronary intervention or cerebral accident (stroke or transient ischaemic attack) within the last 6 months.
Beschrijving

Myocardial Infarction | Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention | Cerebrovascular accident | Transient Ischemic Attack

Datatype

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0010055
UMLS CUI [3]
C1532338
UMLS CUI [4]
C0038454
UMLS CUI [5]
C0007787
has a diagnosis or suspicion of the following conditions: hypertrophic obstructive cardiomyopathy, angina pectoris, chronic heart failure, peripheral arterial occlusive disease, hypertensive retinopathy.
Beschrijving

Hypertrophic Cardiomyopathy | Angina Pectoris | Chronic heart failure | Peripheral arterial occlusive disease | Hypertensive Retinopathy | Hypertrophic Cardiomyopathy Suspicion | Angina Pectoris Suspicion | Chronic heart failure Suspicion | Peripheral arterial occlusive disease Suspicion | Hypertensive Retinopathy Suspicion

Datatype

boolean

Alias
UMLS CUI [1]
C0007194
UMLS CUI [2]
C0002962
UMLS CUI [3]
C0264716
UMLS CUI [4]
C1306889
UMLS CUI [5]
C0152132
UMLS CUI [6,1]
C0007194
UMLS CUI [6,2]
C0242114
UMLS CUI [7,1]
C0002962
UMLS CUI [7,2]
C0242114
UMLS CUI [8,1]
C0264716
UMLS CUI [8,2]
C0242114
UMLS CUI [9,1]
C1306889
UMLS CUI [9,2]
C0242114
UMLS CUI [10,1]
C0152132
UMLS CUI [10,2]
C0242114
has hemodynamically relevant stenosis of the aortic or mitral valve.
Beschrijving

Aortic Valve Stenosis | Mitral Valve Stenosis

Datatype

boolean

Alias
UMLS CUI [1]
C0003507
UMLS CUI [2]
C0026269
has clinically relevant and refractory hypokalaemia or hyperkalaemia.
Beschrijving

Hypokalemia refractory | Hyperkalemia refractory

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020621
UMLS CUI [1,2]
C0205269
UMLS CUI [2,1]
C0020461
UMLS CUI [2,2]
C0205269
has uncorrected volume or sodium depletion.
Beschrijving

Hypovolemia uncorrected | Hyponatremia uncorrected

Datatype

boolean

Alias
UMLS CUI [1,1]
C0546884
UMLS CUI [1,2]
C4072785
UMLS CUI [2,1]
C0020625
UMLS CUI [2,2]
C4072785
has gout or relevant hyperuricaemia.
Beschrijving

Gout | Hyperuricemia

Datatype

boolean

Alias
UMLS CUI [1]
C0018099
UMLS CUI [2]
C0740394
has a known intolerance/hypersensitivity to candesartan cilexetil or hydrochlorothiazide.
Beschrijving

Intolerance to Candesartan cilexetil | Hypersensitivity Candesartan cilexetil | Intolerance to Hydrochlorothiazide | Hydrochlorothiazide allergy

Datatype

boolean

Alias
UMLS CUI [1,1]
C1744706
UMLS CUI [1,2]
C0527379
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0527379
UMLS CUI [3,1]
C1744706
UMLS CUI [3,2]
C0020261
UMLS CUI [4]
C0571898
has a known galactose intolerance, lactase deficiency or glucose-galactose malabsorption.
Beschrijving

Galactosemias | Lactase deficiency | Glucose-galactose malabsorption

Datatype

boolean

Alias
UMLS CUI [1]
C0016952
UMLS CUI [2]
C0302813
UMLS CUI [3]
C0268186
is taking psychotropic medication or is addicted to alcohol or drugs.
Beschrijving

Psychotropic Drugs | Substance Dependence

Datatype

boolean

Alias
UMLS CUI [1]
C0033978
UMLS CUI [2]
C0038580
has participated in another trial of an investigational drug or a medical device within the last 30 days or is currently participating in another trial of an investigational drug or a medical device.
Beschrijving

Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0013230
UMLS CUI [3]
C2346570
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Similar models

Eligibility Hypertension NCT01012479

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Essential Hypertension
Item
confirmed diagnosis of essential hypertension.
boolean
C0085580 (UMLS CUI [1])
Systolic Pressure | Diastolic blood pressure
Item
has systolic blood pressure between 150 mmhg and 200 mmhg and diastolic blood pressure between 110 mmhg and 120 mmhg.
boolean
C0871470 (UMLS CUI [1])
C0428883 (UMLS CUI [2])
Antihypertensive therapy Absent
Item
has not received any antihypertensive treatment so far.
boolean
C0585941 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Childbearing Potential Pregnancy test negative | Females & males of reproductive potential Contraceptive methods
Item
has a negative pregnancy test at baseline in females of childbearing potential. male and female participants with reproductive potential must use an approved contraceptive method during study treatment evaluation
boolean
C3831118 (UMLS CUI [1,1])
C0427780 (UMLS CUI [1,2])
C4034483 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Secondary hypertension | Conn Syndrome | Secondary hypertension Suspected | Conn Syndrome Suspected
Item
has a known or suspected secondary hypertension or primary hyperaldosteronism.
boolean
C0155616 (UMLS CUI [1])
C1384514 (UMLS CUI [2])
C0155616 (UMLS CUI [3,1])
C0750491 (UMLS CUI [3,2])
C1384514 (UMLS CUI [4,1])
C0750491 (UMLS CUI [4,2])
Renal Insufficiency
Item
has impaired renal function.
boolean
C1565489 (UMLS CUI [1])
Hepatic impairment Severe
Item
has severe hepatic impairment.
boolean
C0948807 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Bilateral renal artery stenosis | Kidney Solitary | Status post Kidney Transplantation
Item
has bilateral renal artery stenosis, solitary kidney or post-renal transplant status.
boolean
C0856760 (UMLS CUI [1])
C0022646 (UMLS CUI [2,1])
C0205171 (UMLS CUI [2,2])
C0231290 (UMLS CUI [3,1])
C0022671 (UMLS CUI [3,2])
Myocardial Infarction | Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention | Cerebrovascular accident | Transient Ischemic Attack
Item
has a history of myocardial infarction, coronary artery bypass graft, percutaneous coronary intervention or cerebral accident (stroke or transient ischaemic attack) within the last 6 months.
boolean
C0027051 (UMLS CUI [1])
C0010055 (UMLS CUI [2])
C1532338 (UMLS CUI [3])
C0038454 (UMLS CUI [4])
C0007787 (UMLS CUI [5])
Hypertrophic Cardiomyopathy | Angina Pectoris | Chronic heart failure | Peripheral arterial occlusive disease | Hypertensive Retinopathy | Hypertrophic Cardiomyopathy Suspicion | Angina Pectoris Suspicion | Chronic heart failure Suspicion | Peripheral arterial occlusive disease Suspicion | Hypertensive Retinopathy Suspicion
Item
has a diagnosis or suspicion of the following conditions: hypertrophic obstructive cardiomyopathy, angina pectoris, chronic heart failure, peripheral arterial occlusive disease, hypertensive retinopathy.
boolean
C0007194 (UMLS CUI [1])
C0002962 (UMLS CUI [2])
C0264716 (UMLS CUI [3])
C1306889 (UMLS CUI [4])
C0152132 (UMLS CUI [5])
C0007194 (UMLS CUI [6,1])
C0242114 (UMLS CUI [6,2])
C0002962 (UMLS CUI [7,1])
C0242114 (UMLS CUI [7,2])
C0264716 (UMLS CUI [8,1])
C0242114 (UMLS CUI [8,2])
C1306889 (UMLS CUI [9,1])
C0242114 (UMLS CUI [9,2])
C0152132 (UMLS CUI [10,1])
C0242114 (UMLS CUI [10,2])
Aortic Valve Stenosis | Mitral Valve Stenosis
Item
has hemodynamically relevant stenosis of the aortic or mitral valve.
boolean
C0003507 (UMLS CUI [1])
C0026269 (UMLS CUI [2])
Hypokalemia refractory | Hyperkalemia refractory
Item
has clinically relevant and refractory hypokalaemia or hyperkalaemia.
boolean
C0020621 (UMLS CUI [1,1])
C0205269 (UMLS CUI [1,2])
C0020461 (UMLS CUI [2,1])
C0205269 (UMLS CUI [2,2])
Hypovolemia uncorrected | Hyponatremia uncorrected
Item
has uncorrected volume or sodium depletion.
boolean
C0546884 (UMLS CUI [1,1])
C4072785 (UMLS CUI [1,2])
C0020625 (UMLS CUI [2,1])
C4072785 (UMLS CUI [2,2])
Gout | Hyperuricemia
Item
has gout or relevant hyperuricaemia.
boolean
C0018099 (UMLS CUI [1])
C0740394 (UMLS CUI [2])
Intolerance to Candesartan cilexetil | Hypersensitivity Candesartan cilexetil | Intolerance to Hydrochlorothiazide | Hydrochlorothiazide allergy
Item
has a known intolerance/hypersensitivity to candesartan cilexetil or hydrochlorothiazide.
boolean
C1744706 (UMLS CUI [1,1])
C0527379 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0527379 (UMLS CUI [2,2])
C1744706 (UMLS CUI [3,1])
C0020261 (UMLS CUI [3,2])
C0571898 (UMLS CUI [4])
Galactosemias | Lactase deficiency | Glucose-galactose malabsorption
Item
has a known galactose intolerance, lactase deficiency or glucose-galactose malabsorption.
boolean
C0016952 (UMLS CUI [1])
C0302813 (UMLS CUI [2])
C0268186 (UMLS CUI [3])
Psychotropic Drugs | Substance Dependence
Item
is taking psychotropic medication or is addicted to alcohol or drugs.
boolean
C0033978 (UMLS CUI [1])
C0038580 (UMLS CUI [2])
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device
Item
has participated in another trial of an investigational drug or a medical device within the last 30 days or is currently participating in another trial of an investigational drug or a medical device.
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])
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