Eligibility Congestive Heart Failure NCT00652782

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StudyEvent: Eligibility
1. Eligibility Congestive Heart Failure NCT00652782

Name

Tipo

Description | Question | Decode (Coded Value)

Tipo de dados

Alias

Inclusion Criteria

Item Group

C1512693 (UMLS CUI)

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])

Exclusion Criteria

Item Group

C0680251 (UMLS CUI)

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])

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Eligibility Congestive Heart Failure NCT00652782