Cardiac Arrhythmia | Atrial Fibrillation Duration
Item
must have an abnormal heart rhythm diagnosed as af for less than 48 hours.
boolean
C0003811 (UMLS CUI [1])
C0004238 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
Eligibility Electric Countershock
Item
be eligible for cardioversion (in the judgment of the study doctor).
boolean
C1548635 (UMLS CUI [1,1])
C0013778 (UMLS CUI [1,2])
Anticoagulants Appropriate
Item
are on the appropriate blood thinner medications.
boolean
C0003280 (UMLS CUI [1,1])
C1548787 (UMLS CUI [1,2])
Systolic Pressure | Diastolic blood pressure
Item
have systolic blood pressure (sbp) above 90 mmhg and less than 160 mmhg and diastolic blood pressure (dbp) less than 95 mmhg at screening and baseline.
boolean
C0871470 (UMLS CUI [1])
C0428883 (UMLS CUI [2])
Hydration status | Normal saline Intravenous
Item
are adequately hydrated (in the judgment of the study doctor) and have a normal saline intravenous established and it is working properly.
boolean
C1321013 (UMLS CUI [1])
C0445115 (UMLS CUI [2,1])
C0348016 (UMLS CUI [2,2])
Body Weight
Item
must have a body weight between 45 and 136 kg inclusive (99 and 300 lbs).
boolean
C0005910 (UMLS CUI [1])
Informed Consent
Item
be able and willing to give informed consent.
boolean
C0021430 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnant or nursing a child
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Lung disease Serious | Liver disease Serious | Metabolic Disease Serious | Kidney Disease Serious | Gastrointestinal Disease Serious | CNS disorder Serious | Mental disorders Serious | Communicable Disease | Fever | Terminal illness | Disease Interferes with Completion of clinical trial
Item
are diagnosed with any other serious lung, liver, metabolic, kidney, gastrointestinal, central nervous system, or psychiatric disease, infection, having a fever, end stage disease states, or any other diseases that could interfere with the conduct of this study. your study doctor will confirm this with you.
boolean
C0024115 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0023895 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
C0025517 (UMLS CUI [3,1])
C0205404 (UMLS CUI [3,2])
C0022658 (UMLS CUI [4,1])
C0205404 (UMLS CUI [4,2])
C0017178 (UMLS CUI [5,1])
C0205404 (UMLS CUI [5,2])
C0007682 (UMLS CUI [6,1])
C0205404 (UMLS CUI [6,2])
C0004936 (UMLS CUI [7,1])
C0205404 (UMLS CUI [7,2])
C0009450 (UMLS CUI [8])
C0015967 (UMLS CUI [9])
C0679247 (UMLS CUI [10])
C0012634 (UMLS CUI [11,1])
C0521102 (UMLS CUI [11,2])
C2732579 (UMLS CUI [11,3])
Communicable Disease | Fever
Item
have an infection or fever
boolean
C0009450 (UMLS CUI [1])
C0015967 (UMLS CUI [2])
Procainamide allergy | Propofol allergy
Item
are allergic to procainamide (the chemical conversion agent) or propofol (the sedative agent)
boolean
C0571885 (UMLS CUI [1])
C0570632 (UMLS CUI [2])
Study Subject Participation Status | Investigational New Drugs
Item
are participating in another drug study or have received an experimental drug within 30 days prior to screening in this study
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
Residence Remote
Item
are not currently living in the vancouver coastal health region
boolean
C0237096 (UMLS CUI [1,1])
C0205157 (UMLS CUI [1,2])
Contact with Research Personnel Unable | Contact with Research Personnel Unwilling
Item
are unable or unwilling to be contacted at 30 days by one of the study doctors or study staff to determine 30-day outcomes
boolean
C0332158 (UMLS CUI [1,1])
C0035173 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C0332158 (UMLS CUI [2,1])
C0035173 (UMLS CUI [2,2])
C0558080 (UMLS CUI [2,3])
Informed Consent Unwilling
Item
are unwilling to sign the informed consent form
boolean
C0021430 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
Lacking Able to speak English Language
Item
are unable to speak english
boolean
C0332268 (UMLS CUI [1,1])
C0564215 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,3])