ID

16849

Description

Effects of MK7418 on Diuresis and Renal Function in Congestive Heart Failure Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00652782

Lien

https://clinicaltrials.gov/show/NCT00652782

Mots-clés

Versions (1)
  1. 10/08/2016 10/08/2016 -
Téléchargé le

10 août 2016

DOI

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Licence

Creative Commons BY 4.0
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Eligibility Congestive Heart Failure NCT00652782

Anglais

Eligibility Congestive Heart Failure NCT00652782

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
be able to provide written informed consent,
Description

Informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
be a male or female at least 18 years of age,
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
be hospitalized for fluid overload requiring iv diuretic therapy
Description

Fluid overload Requirement Diuretic therapy Intravenous | Hospitalization

Type de données

boolean

Alias
UMLS CUI [1,1]
C0546817
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0948575
UMLS CUI [1,4]
C0348016
UMLS CUI [2]
C0019993
history of use of diuretic therapy for chf (including this admission),
Description

Diuretic therapy Congestive heart failure

Type de données

boolean

Alias
UMLS CUI [1,1]
C0948575
UMLS CUI [1,2]
C0018802
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
Description

Hospital admission | Furosemide Intravenous

Type de données

boolean

Alias
UMLS CUI [1]
C0184666
UMLS CUI [2,1]
C0016860
UMLS CUI [2,2]
C1522726
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
have had a myocardial infarction within 30 days prior to day -1
Description

Myocardial Infarction

Type de données

boolean

Alias
UMLS CUI [1]
C0027051
be pregnant or breast-feeding
Description

Pregnancy | Breast Feeding

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
have received intravascular contrast material within the preceding 14 days; or have acute contrast nephropathy
Description

Contrast Media Intravascular Received | Contrast - Induced Nephropathy

Type de données

boolean

Alias
UMLS CUI [1,1]
C0009924
UMLS CUI [1,2]
C0442123
UMLS CUI [1,3]
C1514756
UMLS CUI [2]
C4055183
have had implantation of an automated implanted cardiac defibrillator (aicd) or synchronization device within the preceding 7 days
Description

Implantation of automatic cardioverter/defibrillator (AICD) | Implantation Cardiac Resynchronization Therapy Device

Type de données

boolean

Alias
UMLS CUI [1]
C0189864
UMLS CUI [2,1]
C0021107
UMLS CUI [2,2]
C2936377
currently require mechanical ventilation, ultrafiltration, or hemodialysis,
Description

Mechanical ventilation Patient need for | Ultrafiltration Patient need for | Hemodialysis Patient need for

Type de données

boolean

Alias
UMLS CUI [1,1]
C0199470
UMLS CUI [1,2]
C0686904
UMLS CUI [2,1]
C0041612
UMLS CUI [2,2]
C0686904
UMLS CUI [3,1]
C0019004
UMLS CUI [3,2]
C0686904
have symptomatic ventricular tachycardia
Description

VENTRICULAR TACHYCARDIA SYMPTOMATIC

Type de données

boolean

Alias
UMLS CUI [1]
C0750198
be admitted for heart transplant surgery or have had a heart transplant,
Description

Hospital admission Heart Transplantation | Heart Transplantation Previous

Type de données

boolean

Alias
UMLS CUI [1,1]
C0184666
UMLS CUI [1,2]
C0018823
UMLS CUI [2,1]
C0018823
UMLS CUI [2,2]
C0205156
have any other concomitant life-threatening disease,
Description

Comorbidity Life Threatening

Type de données

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C2826244
have participated in a clinical trial of an investigational drug or device within 30 days before randomization
Description

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

Type de données

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0013230
UMLS CUI [3]
C2346570
have a positive urine pregnancy test (for women of child-bearing capacity)
Description

Childbearing Potential Urine pregnancy test positive

Type de données

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0430059
have an allergy to soybean oil and/or eggs
Description

Hypersensitivity Soybean Oil | Hypersensitivity Eggs

Type de données

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0037732
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0013710
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Similar models

Eligibility Congestive Heart Failure NCT00652782

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
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])
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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