ID

24438

Beschrijving

Comparison of Effects of Telmisartan and Valsartan on Neointima Volume in Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT00599885

Link

https://clinicaltrials.gov/show/NCT00599885

Trefwoorden

Versies (1)
  1. 31-07-17 31-07-17 -
Geüploaded op

31 juli 2017

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Hypertension NCT00599885

Engels

Eligibility Hypertension NCT00599885

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
age: 18 years and above
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
gender eligible for study: both
Beschrijving

Gender

Datatype

boolean

Alias
UMLS CUI [1]
C0079399
hypertensive diabetic patients either previously diagnosed or newly found.
Beschrijving

Patients Hypertensive Diabetic

Datatype

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0857121
UMLS CUI [1,3]
C0241863
systolic blood pressure ≥ 130 mmhg or diastolic blood pressure ≥ 80 mmhg for newly found hypertensive patients.
Beschrijving

Systolic Pressure | Diastolic blood pressure | Patients Hypertensive

Datatype

boolean

Alias
UMLS CUI [1]
C0871470
UMLS CUI [2]
C0428883
UMLS CUI [3,1]
C0030705
UMLS CUI [3,2]
C0857121
fasting blood glucose ≥ 126 mg/dl or pp2 blood glucose ≥ 200 mg/dl for newly found diabetes.
Beschrijving

Fasting blood glucose measurement | 2-hour postprandial blood glucose measurement | Diabetes Mellitus

Datatype

boolean

Alias
UMLS CUI [1]
C0428568
UMLS CUI [2]
C2238058
UMLS CUI [3]
C0011849
patients with significant de novo coronary artery disease (diameter stenosis > 70%) requiring stent implantation (angina pectoris and/or exercise-induced ischemia).
Beschrijving

Coronary Artery Disease de novo | Percent Diameter Stenosis Measurement | Placement of stent Patient need for | Angina Pectoris | Ischemia exercise induced

Datatype

boolean

Alias
UMLS CUI [1,1]
C1956346
UMLS CUI [1,2]
C1515568
UMLS CUI [2]
C3897965
UMLS CUI [3,1]
C0522776
UMLS CUI [3,2]
C0686904
UMLS CUI [4]
C0002962
UMLS CUI [5,1]
C0022116
UMLS CUI [5,2]
C0239313
patients with informed consent.
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
acute st-segment elevation myocardial infarction (mi), cto lesions, left main lesions
Beschrijving

ST segment elevation myocardial infarction | Chronic total occlusion of coronary artery Lesion | Left main coronary artery Lesion

Datatype

boolean

Alias
UMLS CUI [1]
C1536220
UMLS CUI [2,1]
C1955779
UMLS CUI [2,2]
C0221198
UMLS CUI [3,1]
C1261082
UMLS CUI [3,2]
C0221198
diabetic patients with the use of thiazolidinediones within 3 months
Beschrijving

Patients Diabetic | Thiazolidinediones

Datatype

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0241863
UMLS CUI [2]
C1257987
previous history of pci or bypass surgery
Beschrijving

Percutaneous Coronary Intervention | Bypass surgery

Datatype

boolean

Alias
UMLS CUI [1]
C1532338
UMLS CUI [2]
C1536078
patients with any contraindications to the treatment of telmisartan or valsartan
Beschrijving

Medical contraindication telmisartan | Medical contraindication valsartan

Datatype

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0248719
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0216784
pregnant or lactating patients
Beschrijving

Pregnancy | Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
chronic alcohol or drug abuse
Beschrijving

Substance Use Disorders chronic

Datatype

boolean

Alias
UMLS CUI [1,1]
C0038586
UMLS CUI [1,2]
C0205191
hepatic dysfunction
Beschrijving

Liver Dysfunction

Datatype

boolean

Alias
UMLS CUI [1]
C0086565
renal dysfunction
Beschrijving

Renal dysfunction

Datatype

boolean

Alias
UMLS CUI [1]
C3279454
heart failure (ef < 50%)
Beschrijving

Heart failure | Cardiac ejection fraction

Datatype

boolean

Alias
UMLS CUI [1]
C0018801
UMLS CUI [2]
C0232174
expected life expectancy of < 1 year
Beschrijving

Life Expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0023671
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Similar models

Eligibility Hypertension NCT00599885

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age: 18 years and above
boolean
C0001779 (UMLS CUI [1])
Gender
Item
gender eligible for study: both
boolean
C0079399 (UMLS CUI [1])
Patients Hypertensive Diabetic
Item
hypertensive diabetic patients either previously diagnosed or newly found.
boolean
C0030705 (UMLS CUI [1,1])
C0857121 (UMLS CUI [1,2])
C0241863 (UMLS CUI [1,3])
Systolic Pressure | Diastolic blood pressure | Patients Hypertensive
Item
systolic blood pressure ≥ 130 mmhg or diastolic blood pressure ≥ 80 mmhg for newly found hypertensive patients.
boolean
C0871470 (UMLS CUI [1])
C0428883 (UMLS CUI [2])
C0030705 (UMLS CUI [3,1])
C0857121 (UMLS CUI [3,2])
Fasting blood glucose measurement | 2-hour postprandial blood glucose measurement | Diabetes Mellitus
Item
fasting blood glucose ≥ 126 mg/dl or pp2 blood glucose ≥ 200 mg/dl for newly found diabetes.
boolean
C0428568 (UMLS CUI [1])
C2238058 (UMLS CUI [2])
C0011849 (UMLS CUI [3])
Coronary Artery Disease de novo | Percent Diameter Stenosis Measurement | Placement of stent Patient need for | Angina Pectoris | Ischemia exercise induced
Item
patients with significant de novo coronary artery disease (diameter stenosis > 70%) requiring stent implantation (angina pectoris and/or exercise-induced ischemia).
boolean
C1956346 (UMLS CUI [1,1])
C1515568 (UMLS CUI [1,2])
C3897965 (UMLS CUI [2])
C0522776 (UMLS CUI [3,1])
C0686904 (UMLS CUI [3,2])
C0002962 (UMLS CUI [4])
C0022116 (UMLS CUI [5,1])
C0239313 (UMLS CUI [5,2])
Informed Consent
Item
patients with informed consent.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
ST segment elevation myocardial infarction | Chronic total occlusion of coronary artery Lesion | Left main coronary artery Lesion
Item
acute st-segment elevation myocardial infarction (mi), cto lesions, left main lesions
boolean
C1536220 (UMLS CUI [1])
C1955779 (UMLS CUI [2,1])
C0221198 (UMLS CUI [2,2])
C1261082 (UMLS CUI [3,1])
C0221198 (UMLS CUI [3,2])
Patients Diabetic | Thiazolidinediones
Item
diabetic patients with the use of thiazolidinediones within 3 months
boolean
C0030705 (UMLS CUI [1,1])
C0241863 (UMLS CUI [1,2])
C1257987 (UMLS CUI [2])
Percutaneous Coronary Intervention | Bypass surgery
Item
previous history of pci or bypass surgery
boolean
C1532338 (UMLS CUI [1])
C1536078 (UMLS CUI [2])
Medical contraindication telmisartan | Medical contraindication valsartan
Item
patients with any contraindications to the treatment of telmisartan or valsartan
boolean
C1301624 (UMLS CUI [1,1])
C0248719 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0216784 (UMLS CUI [2,2])
Pregnancy | Breast Feeding
Item
pregnant or lactating patients
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Substance Use Disorders chronic
Item
chronic alcohol or drug abuse
boolean
C0038586 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
Liver Dysfunction
Item
hepatic dysfunction
boolean
C0086565 (UMLS CUI [1])
Renal dysfunction
Item
renal dysfunction
boolean
C3279454 (UMLS CUI [1])
Heart failure | Cardiac ejection fraction
Item
heart failure (ef < 50%)
boolean
C0018801 (UMLS CUI [1])
C0232174 (UMLS CUI [2])
Life Expectancy
Item
expected life expectancy of < 1 year
boolean
C0023671 (UMLS CUI [1])
Terug naar het begin van de pagina 

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