ID

29974

Description

Trial Comparing Metabolic Effects of Telmisartan and Amlodipine on Hypertensive Patients With Obesity and Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT00847262

Link

https://clinicaltrials.gov/show/NCT00847262

Keywords

Versions (1)
  1. 5/2/18 5/2/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

May 2, 2018

DOI

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License

Creative Commons BY 4.0
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Eligibility Hypertension NCT00847262

English

Eligibility Hypertension NCT00847262

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
information consent signed
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
aged 30~70 years
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
for whom without anti-hypertensive therapy in 2 weeks：140mmhg≤sbp＜180mmhg，或90mmhg≤dbp＜110mmhg. for whom with anti-hypertensive therapies in 2 weeks：sbp＜180mmhg, 且dbp＜110mmhg
Description

Antihypertensive therapy Absent | Antihypertensive therapy | Systolic Pressure | Diastolic blood pressure

Data type

boolean

Alias
UMLS CUI [1,1]
C0585941
UMLS CUI [1,2]
C0332197
UMLS CUI [2]
C0585941
UMLS CUI [3]
C0871470
UMLS CUI [4]
C0428883
waist circumference higher than 90cm in men, 80cm in women
Description

Waist Circumference | Gender

Data type

boolean

Alias
UMLS CUI [1]
C0455829
UMLS CUI [2]
C0079399
diagnosed diabetes
Description

Diabetes Mellitus

Data type

boolean

Alias
UMLS CUI [1]
C0011849
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
grade 3 hypertension: sbp≥180mmhg, or dbp≥110mmhg
Description

Hypertensive disease CTCAE Grades | Systolic Pressure | Diastolic blood pressure

Data type

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C1516728
UMLS CUI [2]
C0871470
UMLS CUI [3]
C0428883
waist circumference less than 90cm in men, 80cm in women
Description

Waist Circumference | Gender

Data type

boolean

Alias
UMLS CUI [1]
C0455829
UMLS CUI [2]
C0079399
known allergy or hypersensitivity to trial drugs
Description

Hypersensitivity Investigational New Drugs

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0013230
nyha grade ⅱ~ⅳ heart failure, myocardial infarction or cerebrovascular accident in 1 year preceding the trial
Description

Heart failure New York Heart Association Classification | Myocardial Infarction | Cerebrovascular accident

Data type

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1275491
UMLS CUI [2]
C0027051
UMLS CUI [3]
C0038454
acute infections, tumor, severe arrhythmia, mental disease, drug or alcohol abuse
Description

Communicable Disease | Malignant Neoplasms | Cardiac Arrhythmia Severe | Mental disorders | Substance Use Disorders

Data type

boolean

Alias
UMLS CUI [1]
C0009450
UMLS CUI [2]
C0006826
UMLS CUI [3,1]
C0003811
UMLS CUI [3,2]
C0205082
UMLS CUI [4]
C0004936
UMLS CUI [5]
C0038586
history of hepatitis or cirrhosis
Description

Hepatitis | Liver Cirrhosis

Data type

boolean

Alias
UMLS CUI [1]
C0019158
UMLS CUI [2]
C0023890
history of severe kidney disease
Description

Kidney Disease Severe

Data type

boolean

Alias
UMLS CUI [1,1]
C0022658
UMLS CUI [1,2]
C0205082
pregnant, lactation
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
enrolled in other trials in 3 months
Description

Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C2348568
any obstacles of follow-up or compliance
Description

Follow-up Limited | Compliance behavior Limited

Data type

boolean

Alias
UMLS CUI [1,1]
C3274571
UMLS CUI [1,2]
C0439801
UMLS CUI [2,1]
C1321605
UMLS CUI [2,2]
C0439801
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Similar models

Eligibility Hypertension NCT00847262

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
information consent signed
boolean
C0021430 (UMLS CUI [1])
Age
Item
aged 30~70 years
boolean
C0001779 (UMLS CUI [1])
Antihypertensive therapy Absent | Antihypertensive therapy | Systolic Pressure | Diastolic blood pressure
Item
for whom without anti-hypertensive therapy in 2 weeks：140mmhg≤sbp＜180mmhg，或90mmhg≤dbp＜110mmhg. for whom with anti-hypertensive therapies in 2 weeks：sbp＜180mmhg, 且dbp＜110mmhg
boolean
C0585941 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0585941 (UMLS CUI [2])
C0871470 (UMLS CUI [3])
C0428883 (UMLS CUI [4])
Waist Circumference | Gender
Item
waist circumference higher than 90cm in men, 80cm in women
boolean
C0455829 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
Diabetes Mellitus
Item
diagnosed diabetes
boolean
C0011849 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Hypertensive disease CTCAE Grades | Systolic Pressure | Diastolic blood pressure
Item
grade 3 hypertension: sbp≥180mmhg, or dbp≥110mmhg
boolean
C0020538 (UMLS CUI [1,1])
C1516728 (UMLS CUI [1,2])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
Waist Circumference | Gender
Item
waist circumference less than 90cm in men, 80cm in women
boolean
C0455829 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
Hypersensitivity Investigational New Drugs
Item
known allergy or hypersensitivity to trial drugs
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
Heart failure New York Heart Association Classification | Myocardial Infarction | Cerebrovascular accident
Item
nyha grade ⅱ~ⅳ heart failure, myocardial infarction or cerebrovascular accident in 1 year preceding the trial
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
C0027051 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
Communicable Disease | Malignant Neoplasms | Cardiac Arrhythmia Severe | Mental disorders | Substance Use Disorders
Item
acute infections, tumor, severe arrhythmia, mental disease, drug or alcohol abuse
boolean
C0009450 (UMLS CUI [1])
C0006826 (UMLS CUI [2])
C0003811 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0004936 (UMLS CUI [4])
C0038586 (UMLS CUI [5])
Hepatitis | Liver Cirrhosis
Item
history of hepatitis or cirrhosis
boolean
C0019158 (UMLS CUI [1])
C0023890 (UMLS CUI [2])
Kidney Disease Severe
Item
history of severe kidney disease
boolean
C0022658 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
pregnant, lactation
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Study Subject Participation Status
Item
enrolled in other trials in 3 months
boolean
C2348568 (UMLS CUI [1])
Follow-up Limited | Compliance behavior Limited
Item
any obstacles of follow-up or compliance
boolean
C3274571 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C1321605 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
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