ID

34228

Beskrivning

Levamlodipine Maleate or Amlodipine Besylate for Treatment of Hypertension: A Comparative Effectiveness Research; ODM derived from: https://clinicaltrials.gov/show/NCT01844570

Länk

https://clinicaltrials.gov/show/NCT01844570

Nyckelord

  1. 2019-01-15 2019-01-15 -
Rättsinnehavare

See clinicaltrials.gov

Uppladdad den

15 januari 2019

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Primary Hypertension NCT01844570

Eligibility Primary Hypertension NCT01844570

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
systolic pressure ≥140mmhg or diastolic pressure ≥90mmhg or receiving antihypertensive drug treatment
Beskrivning

Systolic Pressure | Diastolic blood pressure | Antihypertensive therapy

Datatyp

boolean

Alias
UMLS CUI [1]
C0871470
UMLS CUI [2]
C0428883
UMLS CUI [3]
C0585941
patient himself/herself or his/her family member has already signed the informed consent form
Beskrivning

Informed Consent | Informed Consent Family member

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0086282
patient is fit for use of levamlodipine maleate or amlodipine besylate
Beskrivning

Levamlodipine Malate | Amlodipine Besylate

Datatyp

boolean

Alias
UMLS CUI [1]
C2697915
UMLS CUI [2]
C0354468
age≥45
Beskrivning

Age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient with secondary hypertension
Beskrivning

Secondary hypertension

Datatyp

boolean

Alias
UMLS CUI [1]
C0155616
patients who has suffered from myocardial infarction or stroke within the latest 3 months
Beskrivning

Myocardial Infarction | Cerebrovascular accident

Datatyp

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0038454
patients who has obvious intelligence、hearing and limb's activity disability
Beskrivning

Intelligence Disability | Hearing disability | Limb activity Disability

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0021704
UMLS CUI [1,2]
C0231170
UMLS CUI [2]
C0848765
UMLS CUI [3,1]
C0015385
UMLS CUI [3,2]
C0026606
UMLS CUI [3,3]
C0231170
patients with severe disease, with a life expectancy of less than two years
Beskrivning

Disease Severe | Life Expectancy

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C0023671

Similar models

Eligibility Primary Hypertension NCT01844570

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Systolic Pressure | Diastolic blood pressure | Antihypertensive therapy
Item
systolic pressure ≥140mmhg or diastolic pressure ≥90mmhg or receiving antihypertensive drug treatment
boolean
C0871470 (UMLS CUI [1])
C0428883 (UMLS CUI [2])
C0585941 (UMLS CUI [3])
Informed Consent | Informed Consent Family member
Item
patient himself/herself or his/her family member has already signed the informed consent form
boolean
C0021430 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C0086282 (UMLS CUI [2,2])
Levamlodipine Malate | Amlodipine Besylate
Item
patient is fit for use of levamlodipine maleate or amlodipine besylate
boolean
C2697915 (UMLS CUI [1])
C0354468 (UMLS CUI [2])
Age
Item
age≥45
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Secondary hypertension
Item
patient with secondary hypertension
boolean
C0155616 (UMLS CUI [1])
Myocardial Infarction | Cerebrovascular accident
Item
patients who has suffered from myocardial infarction or stroke within the latest 3 months
boolean
C0027051 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
Intelligence Disability | Hearing disability | Limb activity Disability
Item
patients who has obvious intelligence、hearing and limb's activity disability
boolean
C0021704 (UMLS CUI [1,1])
C0231170 (UMLS CUI [1,2])
C0848765 (UMLS CUI [2])
C0015385 (UMLS CUI [3,1])
C0026606 (UMLS CUI [3,2])
C0231170 (UMLS CUI [3,3])
Disease Severe | Life Expectancy
Item
patients with severe disease, with a life expectancy of less than two years
boolean
C0012634 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0023671 (UMLS CUI [2])

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