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Eligibility Hypertension NCT00932867

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients over 18 years of age
Beskrivning

Age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
arterial hypertension (sbp < 160 mmhg and dbp < 100 mmhg)
Beskrivning

Hypertensive disease | Systolic Pressure | Diastolic blood pressure

Datatyp

boolean

Alias
UMLS CUI [1]
C0020538
UMLS CUI [2]
C0871470
UMLS CUI [3]
C0428883
patients, who do not tolerate ace inhibitors (must be documented in the official ambulant documentation)
Beskrivning

Intolerance to Angiotensin-Converting Enzyme Inhibitors

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1744706
UMLS CUI [1,2]
C0003015
inclusion criteria for the control arm (treated by acei):
Beskrivning

Inclusion criteria Control Arm | Angiotensin-Converting Enzyme Inhibitors

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0009932
UMLS CUI [1,3]
C1522541
UMLS CUI [2]
C0003015
patients over 18 years of age
Beskrivning

Age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
arterial hypertension (sbp < 160 mmhg and dbp < 100 mmhg)
Beskrivning

Hypertensive disease | Systolic Pressure | Diastolic blood pressure

Datatyp

boolean

Alias
UMLS CUI [1]
C0020538
UMLS CUI [2]
C0871470
UMLS CUI [3]
C0428883
patients, who tolerate acei treatment
Beskrivning

Angiotensin-Converting Enzyme Inhibitors Receive Ability

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0003015
UMLS CUI [1,2]
C1514756
UMLS CUI [1,3]
C0085732
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
cholestasis, severe hepatic insufficiency
Beskrivning

Cholestasis | Hepatic Insufficiency Severe

Datatyp

boolean

Alias
UMLS CUI [1]
C0008370
UMLS CUI [2,1]
C1306571
UMLS CUI [2,2]
C0205082
allergy to telmisartan
Beskrivning

Hypersensitivity Telmisartan

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0248719
gravidity or lactation
Beskrivning

Gravidity | Breast Feeding

Datatyp

boolean

Alias
UMLS CUI [1]
C0600457
UMLS CUI [2]
C0006147
exclusion criteria for the arm of patient treated by acei:
Beskrivning

Exclusion Criteria Control Arm | Angiotensin-Converting Enzyme Inhibitors

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C0009932
UMLS CUI [1,3]
C1522541
UMLS CUI [2]
C0003015
cholestasis, severe hepatic insufficiency
Beskrivning

Cholestasis | Hepatic Insufficiency Severe

Datatyp

boolean

Alias
UMLS CUI [1]
C0008370
UMLS CUI [2,1]
C1306571
UMLS CUI [2,2]
C0205082
allergy to acei
Beskrivning

Angiotensin-converting-enzyme inhibitor allergy

Datatyp

boolean

Alias
UMLS CUI [1]
C0571939
gravidity or lactation
Beskrivning

Gravidity | Breast Feeding

Datatyp

boolean

Alias
UMLS CUI [1]
C0600457
UMLS CUI [2]
C0006147
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Similar models

Eligibility Hypertension NCT00932867

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
patients over 18 years of age
boolean
C0001779 (UMLS CUI [1])
Hypertensive disease | Systolic Pressure | Diastolic blood pressure
Item
arterial hypertension (sbp < 160 mmhg and dbp < 100 mmhg)
boolean
C0020538 (UMLS CUI [1])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
Intolerance to Angiotensin-Converting Enzyme Inhibitors
Item
patients, who do not tolerate ace inhibitors (must be documented in the official ambulant documentation)
boolean
C1744706 (UMLS CUI [1,1])
C0003015 (UMLS CUI [1,2])
Inclusion criteria Control Arm | Angiotensin-Converting Enzyme Inhibitors
Item
inclusion criteria for the control arm (treated by acei):
boolean
C1512693 (UMLS CUI [1,1])
C0009932 (UMLS CUI [1,2])
C1522541 (UMLS CUI [1,3])
C0003015 (UMLS CUI [2])
Age
Item
patients over 18 years of age
boolean
C0001779 (UMLS CUI [1])
Hypertensive disease | Systolic Pressure | Diastolic blood pressure
Item
arterial hypertension (sbp < 160 mmhg and dbp < 100 mmhg)
boolean
C0020538 (UMLS CUI [1])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
Angiotensin-Converting Enzyme Inhibitors Receive Ability
Item
patients, who tolerate acei treatment
boolean
C0003015 (UMLS CUI [1,1])
C1514756 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Cholestasis | Hepatic Insufficiency Severe
Item
cholestasis, severe hepatic insufficiency
boolean
C0008370 (UMLS CUI [1])
C1306571 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
Hypersensitivity Telmisartan
Item
allergy to telmisartan
boolean
C0020517 (UMLS CUI [1,1])
C0248719 (UMLS CUI [1,2])
Gravidity | Breast Feeding
Item
gravidity or lactation
boolean
C0600457 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Exclusion Criteria Control Arm | Angiotensin-Converting Enzyme Inhibitors
Item
exclusion criteria for the arm of patient treated by acei:
boolean
C0680251 (UMLS CUI [1,1])
C0009932 (UMLS CUI [1,2])
C1522541 (UMLS CUI [1,3])
C0003015 (UMLS CUI [2])
Cholestasis | Hepatic Insufficiency Severe
Item
cholestasis, severe hepatic insufficiency
boolean
C0008370 (UMLS CUI [1])
C1306571 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
Angiotensin-converting-enzyme inhibitor allergy
Item
allergy to acei
boolean
C0571939 (UMLS CUI [1])
Gravidity | Breast Feeding
Item
gravidity or lactation
boolean
C0600457 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
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