ID

21048

Description

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

Keywords

Versions (1)
  1. 4/5/17 4/5/17 -
Uploaded on

April 5, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Hypertension NCT00281593

English

Eligibility Hypertension NCT00281593

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

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

Age | Hypertensive disease stage

Data type

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
Description

Sitting diastolic blood pressure mean Cuff

Data type

boolean

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

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
breast-feeding
Description

Breast Feeding

Data type

boolean

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

Contraceptive methods Unwilling

Data type

boolean

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

Secondary hypertension

Data type

boolean

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

Systolic Pressure

Data type

boolean

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

Diastolic blood pressure

Data type

boolean

Alias
UMLS CUI [1]
C0428883
severe renal dysfunction
Description

Renal dysfunction Severe

Data type

boolean

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

Hepatic Insufficiency

Data type

boolean

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

Cerebrovascular accident

Data type

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
Description

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

Data type

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
Description

Brittle diabetes | Diabetic - poor control

Data type

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.
Description

Angioedema Investigational Drug Induced | Hypersensitivity Investigational New Drugs

Data type

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
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Similar models

Eligibility Hypertension NCT00281593

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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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