ID

11981

Description

Efficacy and Safety of Olmesartan Associated With Chlorthalidone Versus Losartan Associated With Hydrochlorothiazide (Hyzaar®) in Essential Hypertension Control; ODM derived from: https://clinicaltrials.gov/show/NCT02483936

Link

https://clinicaltrials.gov/show/NCT02483936

Keywords

  1. 8/30/15 8/30/15 -
Copyright Holder

ODM derived from: https://clinicaltrials.gov/show/NCT02483936

Uploaded on

August 30, 2015

DOI

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License

Creative Commons BY 4.0

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Eligibility Arterial Hypertension NCT02483936

Eligibility Arterial Hypertension NCT02483936

Inclusion Criteria
Description

Inclusion Criteria

signed consent of the patient;
Description

consent

Data type

boolean

Alias
UMLS CUI [1]
C0514044
participants with decompensated essential hypertension, classified into stage 1 (with high or very high cardiovascular risk), stage 2 or stage 3 according to the brazilian society of cardiology (2010), who are being treated with monotherapy.
Description

cardiovascular; participants; hypertension; stage; high; very

Data type

boolean

Alias
UMLS CUI [1]
C0085580
Exclusion Criteria
Description

Exclusion Criteria

patients with any clinically significant disease that in the investigator opinion can not participate in the study;
Description

clinically significant; investigator; disease; study

Data type

boolean

Alias
UMLS CUI [1]
C0973444
secondary hypertension diagnosis or blood pressure above 190x100 mmhg in the screening/randomization visit;
Description

blood pressure; randomization; hypertension; diagnosis; screening; visit

Data type

boolean

Alias
UMLS CUI [1]
C0155616
morbid obesity or immunocompromised patients;
Description

immunocompromised; obesity

Data type

boolean

Alias
UMLS CUI [1]
C0085393
UMLS CUI [2]
C0028756
participants with greater than 10 mmhg difference in the measurements of systolic or diastolic blood pressure between the two arms;
Description

diastolic blood pressure; participants; systolic; arms

Data type

boolean

Alias
UMLS CUI [1]
C0151244
participants who do not have the two upper limbs;
Description

participants; upper

Data type

boolean

Alias
UMLS CUI [1]
C1140618
participants with important electrocardiographic changes;
Description

participants

Data type

boolean

Alias
UMLS CUI [1]
C0855329
creatinine clearance - less than 60 ml / min;
Description

creatinine clearance

Data type

boolean

Alias
UMLS CUI [1]
C0373595
history of hypertensive emergencies and cardiovascular and / or moderate to severe cerebrovascular events in the past 6 months;
Description

cardiovascular; moderate; severe; events

Data type

boolean

Alias
UMLS CUI [1]
C0745136
UMLS CUI [2]
C1561291
microalbuminuria urine sample greater than 30 mg/g;
Description

microalbuminuria; urine

Data type

boolean

Alias
UMLS CUI [1]
C0730345
patients with history of hypersensitivity to any of the formula compounds;
Description

history of hypersensitivity to mistletoe

Data type

boolean

Alias
UMLS CUI [1,1]
CL421546
UMLS CUI [1,2]
C0042785
UMLS CUI [1,3]
C0020517
pregnancy or risk of pregnancy and lactation patients;
Description

pregnancy and lactation

Data type

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147
participation in clinical trial in the year prior to this study;
Description

clinical trial; study; year

Data type

boolean

Alias
UMLS CUI [1]
C0008976

Similar models

Eligibility Arterial Hypertension NCT02483936

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
consent
Item
signed consent of the patient;
boolean
C0514044 (UMLS CUI [1])
cardiovascular; participants; hypertension; stage; high; very
Item
participants with decompensated essential hypertension, classified into stage 1 (with high or very high cardiovascular risk), stage 2 or stage 3 according to the brazilian society of cardiology (2010), who are being treated with monotherapy.
boolean
C0085580 (UMLS CUI [1])
clinically significant; investigator; disease; study
Item
patients with any clinically significant disease that in the investigator opinion can not participate in the study;
boolean
C0973444 (UMLS CUI [1])
blood pressure; randomization; hypertension; diagnosis; screening; visit
Item
secondary hypertension diagnosis or blood pressure above 190x100 mmhg in the screening/randomization visit;
boolean
C0155616 (UMLS CUI [1])
immunocompromised; obesity
Item
morbid obesity or immunocompromised patients;
boolean
C0085393 (UMLS CUI [1])
C0028756 (UMLS CUI [2])
diastolic blood pressure; participants; systolic; arms
Item
participants with greater than 10 mmhg difference in the measurements of systolic or diastolic blood pressure between the two arms;
boolean
C0151244 (UMLS CUI [1])
participants; upper
Item
participants who do not have the two upper limbs;
boolean
C1140618 (UMLS CUI [1])
participants
Item
participants with important electrocardiographic changes;
boolean
C0855329 (UMLS CUI [1])
creatinine clearance
Item
creatinine clearance - less than 60 ml / min;
boolean
C0373595 (UMLS CUI [1])
cardiovascular; moderate; severe; events
Item
history of hypertensive emergencies and cardiovascular and / or moderate to severe cerebrovascular events in the past 6 months;
boolean
C0745136 (UMLS CUI [1])
C1561291 (UMLS CUI [2])
microalbuminuria; urine
Item
microalbuminuria urine sample greater than 30 mg/g;
boolean
C0730345 (UMLS CUI [1])
history of hypersensitivity to mistletoe
Item
patients with history of hypersensitivity to any of the formula compounds;
boolean
CL421546 (UMLS CUI [1,1])
C0042785 (UMLS CUI [1,2])
C0020517 (UMLS CUI [1,3])
pregnancy and lactation
Item
pregnancy or risk of pregnancy and lactation patients;
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
clinical trial; study; year
Item
participation in clinical trial in the year prior to this study;
boolean
C0008976 (UMLS CUI [1])

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