ID

36135

Beschrijving

Clinical Characteristics and Medication Satisfaction of Kanarb Tablet in Korean Hypertensive Patient(Kanarb-Hypertension Epidemiology Medication Satisfaction Study); ODM derived from: https://clinicaltrials.gov/show/NCT02394392

Link

https://clinicaltrials.gov/show/NCT02394392

Trefwoorden

  1. 17-04-19 17-04-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

17 april 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Hypertension NCT02394392

Eligibility Hypertension NCT02394392

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
step1
Beschrijving

Step Number

Datatype

boolean

Alias
UMLS CUI [1,1]
C1261552
UMLS CUI [1,2]
C0237753
over 20 years old
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
essential hypertensive patients who taking anti-hypertensive drugs during previous 1 month
Beschrijving

Essential Hypertension | Antihypertensive Agents

Datatype

boolean

Alias
UMLS CUI [1]
C0085580
UMLS CUI [2]
C0003364
step2
Beschrijving

Step Number

Datatype

boolean

Alias
UMLS CUI [1,1]
C1261552
UMLS CUI [1,2]
C0237753
patients does not taking fimasartan
Beschrijving

Fimasartan Absent

Datatype

boolean

Alias
UMLS CUI [1,1]
C2825622
UMLS CUI [1,2]
C0332197
patient's medication satisfaction score under 4
Beschrijving

Satisfaction with Medication Score

Datatype

boolean

Alias
UMLS CUI [1,1]
C3828231
UMLS CUI [1,2]
C0449820
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with secondary hypertension
Beschrijving

Secondary hypertension

Datatype

boolean

Alias
UMLS CUI [1]
C0155616
patients with orthostatic hypotension who has sign and symptom
Beschrijving

Orthostatic Hypotension Signs and Symptoms

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020651
UMLS CUI [1,2]
C0037088
patients with known severe or malignancy retinopathy
Beschrijving

Retinal Disease Severe | Retinal Disease Malignant

Datatype

boolean

Alias
UMLS CUI [1,1]
C0035309
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C0035309
UMLS CUI [2,2]
C0205282
patients with significant investigations; abnormal renal function
Beschrijving

Ivestigation Finding Significant | Abnormal renal function

Datatype

boolean

Alias
UMLS CUI [1,1]
C0243095
UMLS CUI [1,2]
C0750502
UMLS CUI [2]
C0151746
childbearing and breast-feeding women
Beschrijving

Pregnancy | Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
patients with history of allergic reaction to any angiotensin ii antagonist
Beschrijving

Allergy to angiotensin II receptor antagonist

Datatype

boolean

Alias
UMLS CUI [1]
C2585204

Similar models

Eligibility Hypertension NCT02394392

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Step Number
Item
step1
boolean
C1261552 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
Age
Item
over 20 years old
boolean
C0001779 (UMLS CUI [1])
Essential Hypertension | Antihypertensive Agents
Item
essential hypertensive patients who taking anti-hypertensive drugs during previous 1 month
boolean
C0085580 (UMLS CUI [1])
C0003364 (UMLS CUI [2])
Step Number
Item
step2
boolean
C1261552 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
Fimasartan Absent
Item
patients does not taking fimasartan
boolean
C2825622 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Satisfaction with Medication Score
Item
patient's medication satisfaction score under 4
boolean
C3828231 (UMLS CUI [1,1])
C0449820 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Secondary hypertension
Item
patients with secondary hypertension
boolean
C0155616 (UMLS CUI [1])
Orthostatic Hypotension Signs and Symptoms
Item
patients with orthostatic hypotension who has sign and symptom
boolean
C0020651 (UMLS CUI [1,1])
C0037088 (UMLS CUI [1,2])
Retinal Disease Severe | Retinal Disease Malignant
Item
patients with known severe or malignancy retinopathy
boolean
C0035309 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0035309 (UMLS CUI [2,1])
C0205282 (UMLS CUI [2,2])
Ivestigation Finding Significant | Abnormal renal function
Item
patients with significant investigations; abnormal renal function
boolean
C0243095 (UMLS CUI [1,1])
C0750502 (UMLS CUI [1,2])
C0151746 (UMLS CUI [2])
Pregnancy | Breast Feeding
Item
childbearing and breast-feeding women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Allergy to angiotensin II receptor antagonist
Item
patients with history of allergic reaction to any angiotensin ii antagonist
boolean
C2585204 (UMLS CUI [1])

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