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])
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])