ID

21056

Beschrijving

Clevidipine in the Treatment of Patients With Severe Hypertension (VELOCITY); ODM derived from: https://clinicaltrials.gov/show/NCT00369837

Link

https://clinicaltrials.gov/show/NCT00369837

Trefwoorden

Versies (1)
  1. 06-04-17 06-04-17 -
Geüploaded op

6 april 2017

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Hypertension NCT00369837

Engels

Eligibility Hypertension NCT00369837

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
age 18 years or older
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
systolic blood pressure >180 mmhg and/or diastolic blood pressure >115 mmhg assessed on two successive occasions, 15 minutes apart at baseline
Beschrijving

Systolic Pressure | Diastolic blood pressure

Datatype

boolean

Alias
UMLS CUI [1]
C0871470
UMLS CUI [2]
C0428883
written informed consent
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
sbp ≤180 mmhg and/or dbp ≤115 mmhg
Beschrijving

Systolic Pressure | Diastolic blood pressure

Datatype

boolean

Alias
UMLS CUI [1]
C0871470
UMLS CUI [2]
C0428883
expectation that the patient will not tolerate intravenous antihypertensive therapy for at least 18 hours
Beschrijving

Intolerance Antihypertensive therapy Intravenous

Datatype

boolean

Alias
UMLS CUI [1,1]
C1744706
UMLS CUI [1,2]
C0585941
UMLS CUI [1,3]
C1522726
UMLS CUI [1,4]
C1744706
known or suspected aortic dissection
Beschrijving

Dissection of aorta | Dissection of aorta Suspected

Datatype

boolean

Alias
UMLS CUI [1]
C0340643
UMLS CUI [2,1]
C0340643
UMLS CUI [2,2]
C0750491
administration of an agent for treating hypertension within 2 hours of clevidipine administration
Beschrijving

Pharmaceutical Preparation Hypertensive disease | clevidipine

Datatype

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0020538
UMLS CUI [2]
C0766108
severe hypertension known to be precipitated by use of, or withdrawal from, alcohol or illicit drugs, or intentional overdose of illicit or prescription drugs
Beschrijving

Severe hypertension Due to Alcohol consumption | Severe hypertension Due to Illicit drug use | Severe hypertension Due to Alcohol consumption Withdrawal | Severe hypertension Due to Illicit drug use Withdrawal | Severe hypertension Due to Illicit drug overdose intentional | Severe hypertension Due to Intentional drug overdose

Datatype

boolean

Alias
UMLS CUI [1,1]
C4013784
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0001948
UMLS CUI [2,1]
C4013784
UMLS CUI [2,2]
C0678226
UMLS CUI [2,3]
C0281875
UMLS CUI [3,1]
C4013784
UMLS CUI [3,2]
C0678226
UMLS CUI [3,3]
C0001948
UMLS CUI [3,4]
C2349954
UMLS CUI [4,1]
C4013784
UMLS CUI [4,2]
C0678226
UMLS CUI [4,3]
C0281875
UMLS CUI [4,4]
C2349954
UMLS CUI [5,1]
C4013784
UMLS CUI [5,2]
C0678226
UMLS CUI [5,3]
C3872526
UMLS CUI [5,4]
C1283828
UMLS CUI [6,1]
C4013784
UMLS CUI [6,2]
C0678226
UMLS CUI [6,3]
C0520804
positive pregnancy test
Beschrijving

Pregnancy test positive

Datatype

boolean

Alias
UMLS CUI [1]
C0240802
intolerance to calcium channel blockers
Beschrijving

intolerance to Calcium Channel Blockers

Datatype

boolean

Alias
UMLS CUI [1,1]
C1744706
UMLS CUI [1,2]
C0006684
allergy to soybean oil or egg lecithin
Beschrijving

Hypersensitivity Soybean Oil | Hypersensitivity egg lecithin

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0037732
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0772274
known liver failure or cirrhosis
Beschrijving

Liver Failure | Liver Cirrhosis

Datatype

boolean

Alias
UMLS CUI [1]
C0085605
UMLS CUI [2]
C0023890
participation in clinical research studies of other investigational drugs or devices within 30 days of enrollment
Beschrijving

Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0013230
UMLS CUI [3]
C2346570
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Similar models

Eligibility Hypertension NCT00369837

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age 18 years or older
boolean
C0001779 (UMLS CUI [1])
Systolic Pressure | Diastolic blood pressure
Item
systolic blood pressure >180 mmhg and/or diastolic blood pressure >115 mmhg assessed on two successive occasions, 15 minutes apart at baseline
boolean
C0871470 (UMLS CUI [1])
C0428883 (UMLS CUI [2])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Systolic Pressure | Diastolic blood pressure
Item
sbp ≤180 mmhg and/or dbp ≤115 mmhg
boolean
C0871470 (UMLS CUI [1])
C0428883 (UMLS CUI [2])
Intolerance Antihypertensive therapy Intravenous
Item
expectation that the patient will not tolerate intravenous antihypertensive therapy for at least 18 hours
boolean
C1744706 (UMLS CUI [1,1])
C0585941 (UMLS CUI [1,2])
C1522726 (UMLS CUI [1,3])
C1744706 (UMLS CUI [1,4])
Dissection of aorta | Dissection of aorta Suspected
Item
known or suspected aortic dissection
boolean
C0340643 (UMLS CUI [1])
C0340643 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
Pharmaceutical Preparation Hypertensive disease | clevidipine
Item
administration of an agent for treating hypertension within 2 hours of clevidipine administration
boolean
C0013227 (UMLS CUI [1,1])
C0020538 (UMLS CUI [1,2])
C0766108 (UMLS CUI [2])
Severe hypertension Due to Alcohol consumption | Severe hypertension Due to Illicit drug use | Severe hypertension Due to Alcohol consumption Withdrawal | Severe hypertension Due to Illicit drug use Withdrawal | Severe hypertension Due to Illicit drug overdose intentional | Severe hypertension Due to Intentional drug overdose
Item
severe hypertension known to be precipitated by use of, or withdrawal from, alcohol or illicit drugs, or intentional overdose of illicit or prescription drugs
boolean
C4013784 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0001948 (UMLS CUI [1,3])
C4013784 (UMLS CUI [2,1])
C0678226 (UMLS CUI [2,2])
C0281875 (UMLS CUI [2,3])
C4013784 (UMLS CUI [3,1])
C0678226 (UMLS CUI [3,2])
C0001948 (UMLS CUI [3,3])
C2349954 (UMLS CUI [3,4])
C4013784 (UMLS CUI [4,1])
C0678226 (UMLS CUI [4,2])
C0281875 (UMLS CUI [4,3])
C2349954 (UMLS CUI [4,4])
C4013784 (UMLS CUI [5,1])
C0678226 (UMLS CUI [5,2])
C3872526 (UMLS CUI [5,3])
C1283828 (UMLS CUI [5,4])
C4013784 (UMLS CUI [6,1])
C0678226 (UMLS CUI [6,2])
C0520804 (UMLS CUI [6,3])
Pregnancy test positive
Item
positive pregnancy test
boolean
C0240802 (UMLS CUI [1])
intolerance to Calcium Channel Blockers
Item
intolerance to calcium channel blockers
boolean
C1744706 (UMLS CUI [1,1])
C0006684 (UMLS CUI [1,2])
Hypersensitivity Soybean Oil | Hypersensitivity egg lecithin
Item
allergy to soybean oil or egg lecithin
boolean
C0020517 (UMLS CUI [1,1])
C0037732 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0772274 (UMLS CUI [2,2])
Liver Failure | Liver Cirrhosis
Item
known liver failure or cirrhosis
boolean
C0085605 (UMLS CUI [1])
C0023890 (UMLS CUI [2])
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device
Item
participation in clinical research studies of other investigational drugs or devices within 30 days of enrollment
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])
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