ID

15847

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT00529750

Nyckelord

  1. 2016-06-15 2016-06-15 -
Uppladdad den

15 juni 2016

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Hypertension NCT00529750

Eligibility Hypertension NCT00529750

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
hypertension grade 1 or 2
Beskrivning

hypertension

Datatyp

boolean

Alias
UMLS CUI [1]
C0020538
with at least two of the following criteria for the diagnosis of metabolic syndrome:
Beskrivning

metabolic syndrome

Datatyp

boolean

Alias
UMLS CUI [1]
C2229034
body mass index > or = 25 kg/m2 and waist circumference > or = 100 cm.
Beskrivning

body mass index

Datatyp

boolean

Alias
UMLS CUI [1]
C1305855
UMLS CUI [2]
C0455829
dyslipidemia (triglycerides fasting serum levels > or = 200 mg/dl or hdl serum levels < or = 40 mg/dl)
Beskrivning

dyslipidemia

Datatyp

boolean

Alias
UMLS CUI [1]
C0242339
fasting serum glucose > or = 110 mg/dl but < 126 mg/dl
Beskrivning

fasting serum glucose

Datatyp

boolean

Alias
UMLS CUI [1]
C0583334
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
known hypersensitivity to irbesartan
Beskrivning

hypersensitivity to irbesartan

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0288171
hypertension grade 3
Beskrivning

hypertension grade 3

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C0450094
history of clinical vascular events such as tias, stroke, peripheral arterial disease
Beskrivning

clinical vascular events

Datatyp

boolean

Alias
UMLS CUI [1]
C0007787
UMLS CUI [2]
C0038454
UMLS CUI [3]
C1704436
coronary artery disease
Beskrivning

coronary artery disease

Datatyp

boolean

Alias
UMLS CUI [1]
C1956346
renal insufficiency (creatinine serum levels > or = 1.2 mg/dl)
Beskrivning

renal insufficiency

Datatyp

boolean

Alias
UMLS CUI [1]
C0201976
presence of clinical heart failure
Beskrivning

heart failure

Datatyp

boolean

Alias
UMLS CUI [1]
C0018801
asthma and copd
Beskrivning

asthma and copd

Datatyp

boolean

Alias
UMLS CUI [1]
C0004096
UMLS CUI [2]
C0024117
valvular cardiopathy clinically relevant
Beskrivning

valvular cardiopathy

Datatyp

boolean

Alias
UMLS CUI [1]
C1392010
current therapy with antioxidant drugs, statins
Beskrivning

antioxidant drugs

Datatyp

boolean

Alias
UMLS CUI [1]
C0003402
UMLS CUI [2]
C0360714
therapy with aiira for at least 3 months during the last semester
Beskrivning

aiira

Datatyp

boolean

Alias
UMLS CUI [1]
C0521942
presence of any acute illness or major trauma in the last 8 weeks
Beskrivning

acute illness or major trauma

Datatyp

boolean

Alias
UMLS CUI [1]
C0009488
history of a chronic inflammatory disease such as rheumatoid arthritis, immune disorders or connective tissue disease.
Beskrivning

chronic inflammatory disease

Datatyp

boolean

Alias
UMLS CUI [1]
C1290886
UMLS CUI [2]
C0003873
UMLS CUI [3]
C0004364
UMLS CUI [4]
C0009782
the above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Beskrivning

exclusion criteria

Datatyp

boolean

Similar models

Eligibility Hypertension NCT00529750

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
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])
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])
Item Group
C0680251 (UMLS CUI)
hypersensitivity to irbesartan
Item
known hypersensitivity to irbesartan
boolean
C0020517 (UMLS CUI [1,1])
C0288171 (UMLS CUI [1,2])
hypertension grade 3
Item
hypertension grade 3
boolean
C0020538 (UMLS CUI [1,1])
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])
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])
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])
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])
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

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