ID

21048

Beschrijving

Telmisartan (Micardis) and Ramipril (Altace) - Factorial Design Study for the Treatment of Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT00281593

Link

https://clinicaltrials.gov/show/NCT00281593

Trefwoorden

  1. 05-04-17 05-04-17 -
Geüploaded op

5 april 2017

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Hypertension NCT00281593

Eligibility Hypertension NCT00281593

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
male and female patients >=18 years of age with stage i or ii hypertension defined as:
Beschrijving

Age | Hypertensive disease stage

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2,1]
C0020538
UMLS CUI [2,2]
C0699749
a mean seated cuff diastolic blood pressure >=95 and <=119 mmhg main
Beschrijving

Sitting diastolic blood pressure mean Cuff

Datatype

boolean

Alias
UMLS CUI [1,1]
C1319894
UMLS CUI [1,2]
C0444504
UMLS CUI [1,3]
C0441107
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant
Beschrijving

Pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
breast-feeding
Beschrijving

Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0006147
unwilling to use birth control during the study
Beschrijving

Contraceptive methods Unwilling

Datatype

boolean

Alias
UMLS CUI [1,1]
C0700589
UMLS CUI [1,2]
C0558080
secondary hypertension
Beschrijving

Secondary hypertension

Datatype

boolean

Alias
UMLS CUI [1]
C0155616
sbp>=180 mmhg
Beschrijving

Systolic Pressure

Datatype

boolean

Alias
UMLS CUI [1]
C0871470
dbp>=120 mmhg
Beschrijving

Diastolic blood pressure

Datatype

boolean

Alias
UMLS CUI [1]
C0428883
severe renal dysfunction
Beschrijving

Renal dysfunction Severe

Datatype

boolean

Alias
UMLS CUI [1,1]
C3279454
UMLS CUI [1,2]
C0205082
hepatic insufficiency
Beschrijving

Hepatic Insufficiency

Datatype

boolean

Alias
UMLS CUI [1]
C1306571
stroke within the last 6 months
Beschrijving

Cerebrovascular accident

Datatype

boolean

Alias
UMLS CUI [1]
C0038454
myocardial infarction, cardiac surgery, percutaneous transluminal coronary angioplasty, unstable angina or coronary artery bypass graft within the past three months
Beschrijving

Myocardial Infarction | Cardiac Surgery | Percutaneous Transluminal Coronary Angioplasty | Angina, Unstable | Coronary Artery Bypass Surgery

Datatype

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0018821
UMLS CUI [3]
C2936173
UMLS CUI [4]
C0002965
UMLS CUI [5]
C0010055
unstable or uncontrolled diabetes
Beschrijving

Brittle diabetes | Diabetic - poor control

Datatype

boolean

Alias
UMLS CUI [1]
C0342302
UMLS CUI [2]
C0421258
history of angioedema of either of the study drugs, and hypersensitivity to the study drugs.
Beschrijving

Angioedema Investigational Drug Induced | Hypersensitivity Investigational New Drugs

Datatype

boolean

Alias
UMLS CUI [1,1]
C0002994
UMLS CUI [1,2]
C0013230
UMLS CUI [1,3]
C0205263
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0013230

Similar models

Eligibility Hypertension NCT00281593

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age | Hypertensive disease stage
Item
male and female patients >=18 years of age with stage i or ii hypertension defined as:
boolean
C0001779 (UMLS CUI [1])
C0020538 (UMLS CUI [2,1])
C0699749 (UMLS CUI [2,2])
Sitting diastolic blood pressure mean Cuff
Item
a mean seated cuff diastolic blood pressure >=95 and <=119 mmhg main
boolean
C1319894 (UMLS CUI [1,1])
C0444504 (UMLS CUI [1,2])
C0441107 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Pregnancy
Item
pregnant
boolean
C0032961 (UMLS CUI [1])
Breast Feeding
Item
breast-feeding
boolean
C0006147 (UMLS CUI [1])
Contraceptive methods Unwilling
Item
unwilling to use birth control during the study
boolean
C0700589 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
Secondary hypertension
Item
secondary hypertension
boolean
C0155616 (UMLS CUI [1])
Systolic Pressure
Item
sbp>=180 mmhg
boolean
C0871470 (UMLS CUI [1])
Diastolic blood pressure
Item
dbp>=120 mmhg
boolean
C0428883 (UMLS CUI [1])
Renal dysfunction Severe
Item
severe renal dysfunction
boolean
C3279454 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Hepatic Insufficiency
Item
hepatic insufficiency
boolean
C1306571 (UMLS CUI [1])
Cerebrovascular accident
Item
stroke within the last 6 months
boolean
C0038454 (UMLS CUI [1])
Myocardial Infarction | Cardiac Surgery | Percutaneous Transluminal Coronary Angioplasty | Angina, Unstable | Coronary Artery Bypass Surgery
Item
myocardial infarction, cardiac surgery, percutaneous transluminal coronary angioplasty, unstable angina or coronary artery bypass graft within the past three months
boolean
C0027051 (UMLS CUI [1])
C0018821 (UMLS CUI [2])
C2936173 (UMLS CUI [3])
C0002965 (UMLS CUI [4])
C0010055 (UMLS CUI [5])
Brittle diabetes | Diabetic - poor control
Item
unstable or uncontrolled diabetes
boolean
C0342302 (UMLS CUI [1])
C0421258 (UMLS CUI [2])
Angioedema Investigational Drug Induced | Hypersensitivity Investigational New Drugs
Item
history of angioedema of either of the study drugs, and hypersensitivity to the study drugs.
boolean
C0002994 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C0205263 (UMLS CUI [1,3])
C0020517 (UMLS CUI [2,1])
C0013230 (UMLS CUI [2,2])

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