Informatie:
Fout:
ID
29974
Beschrijving
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
Trefwoorden
Versies (1)
- 02-05-18 02-05-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
2 mei 2018
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Hypertension NCT00847262
Eligibility Hypertension NCT00847262
- StudyEvent: Eligibility
Similar models
Eligibility Hypertension NCT00847262
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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])
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])
C0079399 (UMLS CUI [2])
Diabetes Mellitus
Item
diagnosed diabetes
boolean
C0011849 (UMLS CUI [1])
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])
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])
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])
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])
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])
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])
C0023890 (UMLS CUI [2])
Kidney Disease Severe
Item
history of severe kidney disease
boolean
C0022658 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
pregnant, lactation
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
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])
C0439801 (UMLS CUI [1,2])
C1321605 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])