ID

16849

Beschreibung

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

Link

https://clinicaltrials.gov/show/NCT00652782

Stichworte

Versionen (1)
  1. 10.08.16 10.08.16 -
Hochgeladen am

10. August 2016

DOI

Für eine Beantragung loggen Sie sich ein.

Lizenz

Creative Commons BY 4.0
Modell Kommentare :

Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.

Zurück zu Modell Kommentaren
Itemgroup Kommentare für :

Item Kommentare für :

Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.

Eligibility Congestive Heart Failure NCT00652782

Englisch

Eligibility Congestive Heart Failure NCT00652782

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

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

Informed consent

Datentyp

boolean

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

Age

Datentyp

boolean

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

Fluid overload Requirement Diuretic therapy Intravenous | Hospitalization

Datentyp

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),
Beschreibung

Diuretic therapy Congestive heart failure

Datentyp

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
Beschreibung

Hospital admission | Furosemide Intravenous

Datentyp

boolean

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

Exclusion Criteria

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

Myocardial Infarction

Datentyp

boolean

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

Pregnancy | Breast Feeding

Datentyp

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
Beschreibung

Contrast Media Intravascular Received | Contrast - Induced Nephropathy

Datentyp

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
Beschreibung

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

Datentyp

boolean

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

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

Datentyp

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
Beschreibung

VENTRICULAR TACHYCARDIA SYMPTOMATIC

Datentyp

boolean

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

Hospital admission Heart Transplantation | Heart Transplantation Previous

Datentyp

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,
Beschreibung

Comorbidity Life Threatening

Datentyp

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
Beschreibung

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

Datentyp

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)
Beschreibung

Childbearing Potential Urine pregnancy test positive

Datentyp

boolean

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

Hypersensitivity Soybean Oil | Hypersensitivity Eggs

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0037732
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0013710
Zum Seitenanfang zurückkehren

Ähnliche Modelle

Eligibility Congestive Heart Failure NCT00652782

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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])
Zum Seitenanfang zurückkehren 

Kontakt

Benutzen Sie dieses Formular für Rückmeldungen, Fragen und Verbesserungsvorschläge.

Mit * gekennzeichnete Felder sind notwendig.

Hilfe

Benötigen Sie Hilfe bei der Suche? Um mehr Details zu erfahren und die Suche effektiver nutzen zu können schauen Sie sich doch das entsprechende Video auf unserer Tutorial Seite an.

Zum Video