Informatie:
Fout:
ID
15847
Beschrijving
Effect of the Angiotensin II Receptor Antagonist Irbesartan on Biochemical and Functional Markers of Endothelial Dysfunction in Patients With Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT00529750
Link
https://clinicaltrials.gov/show/NCT00529750
Trefwoorden
Versies (1)
- 15-06-16 15-06-16 -
Geüploaded op
15 juni 2016
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Hypertension NCT00529750
Eligibility Hypertension NCT00529750
- StudyEvent: Eligibility
Similar models
Eligibility Hypertension NCT00529750
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
hypertension
Item
hypertension grade 1 or 2
boolean
C0020538 (UMLS CUI [1])
metabolic syndrome
Item
with at least two of the following criteria for the diagnosis of metabolic syndrome:
boolean
C2229034 (UMLS CUI [1])
body mass index
Item
body mass index > or = 25 kg/m2 and waist circumference > or = 100 cm.
boolean
C1305855 (UMLS CUI [1])
C0455829 (UMLS CUI [2])
C0455829 (UMLS CUI [2])
dyslipidemia
Item
dyslipidemia (triglycerides fasting serum levels > or = 200 mg/dl or hdl serum levels < or = 40 mg/dl)
boolean
C0242339 (UMLS CUI [1])
fasting serum glucose
Item
fasting serum glucose > or = 110 mg/dl but < 126 mg/dl
boolean
C0583334 (UMLS CUI [1])
hypersensitivity to irbesartan
Item
known hypersensitivity to irbesartan
boolean
C0020517 (UMLS CUI [1,1])
C0288171 (UMLS CUI [1,2])
C0288171 (UMLS CUI [1,2])
hypertension grade 3
Item
hypertension grade 3
boolean
C0020538 (UMLS CUI [1,1])
C0450094 (UMLS CUI [1,2])
C0450094 (UMLS CUI [1,2])
clinical vascular events
Item
history of clinical vascular events such as tias, stroke, peripheral arterial disease
boolean
C0007787 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
C1704436 (UMLS CUI [3])
C0038454 (UMLS CUI [2])
C1704436 (UMLS CUI [3])
coronary artery disease
Item
coronary artery disease
boolean
C1956346 (UMLS CUI [1])
renal insufficiency
Item
renal insufficiency (creatinine serum levels > or = 1.2 mg/dl)
boolean
C0201976 (UMLS CUI [1])
heart failure
Item
presence of clinical heart failure
boolean
C0018801 (UMLS CUI [1])
asthma and copd
Item
asthma and copd
boolean
C0004096 (UMLS CUI [1])
C0024117 (UMLS CUI [2])
C0024117 (UMLS CUI [2])
valvular cardiopathy
Item
valvular cardiopathy clinically relevant
boolean
C1392010 (UMLS CUI [1])
antioxidant drugs
Item
current therapy with antioxidant drugs, statins
boolean
C0003402 (UMLS CUI [1])
C0360714 (UMLS CUI [2])
C0360714 (UMLS CUI [2])
aiira
Item
therapy with aiira for at least 3 months during the last semester
boolean
C0521942 (UMLS CUI [1])
acute illness or major trauma
Item
presence of any acute illness or major trauma in the last 8 weeks
boolean
C0009488 (UMLS CUI [1])
chronic inflammatory disease
Item
history of a chronic inflammatory disease such as rheumatoid arthritis, immune disorders or connective tissue disease.
boolean
C1290886 (UMLS CUI [1])
C0003873 (UMLS CUI [2])
C0004364 (UMLS CUI [3])
C0009782 (UMLS CUI [4])
C0003873 (UMLS CUI [2])
C0004364 (UMLS CUI [3])
C0009782 (UMLS CUI [4])
exclusion criteria
Item
the above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
boolean