Informed consent
Item
be able to provide written informed consent,
boolean
C0021430 (UMLS CUI [1])
Age
Item
be a male or female at least 18 years of age,
boolean
C0001779 (UMLS CUI [1])
Fluid overload Requirement Diuretic therapy Intravenous | Hospitalization
Item
be hospitalized for fluid overload requiring iv diuretic therapy
boolean
C0546817 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0948575 (UMLS CUI [1,3])
C0348016 (UMLS CUI [1,4])
C0019993 (UMLS CUI [2])
Diuretic therapy Congestive heart failure
Item
history of use of diuretic therapy for chf (including this admission),
boolean
C0948575 (UMLS CUI [1,1])
C0018802 (UMLS CUI [1,2])
Hospital admission | Furosemide Intravenous
Item
be admitted to the hospital within 36 hours of the mandatory dose of iv furosemide 40 mg at between 2000 and 2200 hour on day -1
boolean
C0184666 (UMLS CUI [1])
C0016860 (UMLS CUI [2,1])
C1522726 (UMLS CUI [2,2])
Myocardial Infarction
Item
have had a myocardial infarction within 30 days prior to day -1
boolean
C0027051 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
be pregnant or breast-feeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Contrast Media Intravascular Received | Contrast - Induced Nephropathy
Item
have received intravascular contrast material within the preceding 14 days; or have acute contrast nephropathy
boolean
C0009924 (UMLS CUI [1,1])
C0442123 (UMLS CUI [1,2])
C1514756 (UMLS CUI [1,3])
C4055183 (UMLS CUI [2])
Implantation of automatic cardioverter/defibrillator (AICD) | Implantation Cardiac Resynchronization Therapy Device
Item
have had implantation of an automated implanted cardiac defibrillator (aicd) or synchronization device within the preceding 7 days
boolean
C0189864 (UMLS CUI [1])
C0021107 (UMLS CUI [2,1])
C2936377 (UMLS CUI [2,2])
Mechanical ventilation Patient need for | Ultrafiltration Patient need for | Hemodialysis Patient need for
Item
currently require mechanical ventilation, ultrafiltration, or hemodialysis,
boolean
C0199470 (UMLS CUI [1,1])
C0686904 (UMLS CUI [1,2])
C0041612 (UMLS CUI [2,1])
C0686904 (UMLS CUI [2,2])
C0019004 (UMLS CUI [3,1])
C0686904 (UMLS CUI [3,2])
VENTRICULAR TACHYCARDIA SYMPTOMATIC
Item
have symptomatic ventricular tachycardia
boolean
C0750198 (UMLS CUI [1])
Hospital admission Heart Transplantation | Heart Transplantation Previous
Item
be admitted for heart transplant surgery or have had a heart transplant,
boolean
C0184666 (UMLS CUI [1,1])
C0018823 (UMLS CUI [1,2])
C0018823 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
Comorbidity Life Threatening
Item
have any other concomitant life-threatening disease,
boolean
C0009488 (UMLS CUI [1,1])
C2826244 (UMLS CUI [1,2])
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device
Item
have participated in a clinical trial of an investigational drug or device within 30 days before randomization
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])
Childbearing Potential Urine pregnancy test positive
Item
have a positive urine pregnancy test (for women of child-bearing capacity)
boolean
C3831118 (UMLS CUI [1,1])
C0430059 (UMLS CUI [1,2])
Hypersensitivity Soybean Oil | Hypersensitivity Eggs
Item
have an allergy to soybean oil and/or eggs
boolean
C0020517 (UMLS CUI [1,1])
C0037732 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0013710 (UMLS CUI [2,2])