ID

12587

Descrizione

Gas Exchange for Predicting Hospital Heart Failure Readmissions; ODM derived from: https://clinicaltrials.gov/show/NCT01960218

collegamento

https://clinicaltrials.gov/show/NCT01960218

Keywords

versioni (1)
  1. 03/12/15 03/12/15 -
Caricato su

3 dicembre 2015

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0
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Eligibility Acute Decompensated Heart Failure NCT01960218

Inglese

Eligibility Acute Decompensated Heart Failure NCT01960218

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
subject is 18 years and older
Descrizione

Age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
subject is hospitalized for acute decompensated heart failure (adhf)
Descrizione

hospitalized for acute decompensated heart failure

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1609524
UMLS CUI [2]
C0019993
subject is stage c:class ii/iii/iv systolic or diastolic heart failure
Descrizione

subject is stage c:class ii/iii/iv systolic or diastolic heart failure

Tipo di dati

boolean

Alias
UMLS CUI [1]
C3531729
UMLS CUI [2]
C3531731
subject is willing and to provide appropriate informed consent
Descrizione

informed consent

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021430
subject is willing and able to comply with the requirements of the protocol, including follow-up evaluations and schedule
Descrizione

compliance behavior

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1321605
subject is willing to use the shape-hf cardiopulmonary exercise testing system
Descrizione

compliance behavior

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1321605
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
the subject is pregnant (verified in a manner consistent with institution's standard of care)
Descrizione

Pregnancy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0549206
subject is currently participating in another investigational device or drug trial
Descrizione

currently participating in another investigational device or drug trial

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2348568
subject is a prisoner, a minor or unable to adequately give informed consent due to mental or physical condition
Descrizione

subject is a prisoner, a minor or unable to adequately give informed consent

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2]
C0439801
UMLS CUI [3]
C0009488
subject is unwilling or unable to return for the required follow-up after test
Descrizione

subject is unwilling or unable to return for the required follow-up

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1321605
subject has left ventricular assist device (lvad)
Descrizione

left ventricular assist device

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0181598
subject is listed for transplant
Descrizione

listed for transplant

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0040732
subject has a clinical diagnosis of acute myocardial infarction (ami) on admission (note: if troponin measurements have been collected and are elevated but not due to an mi subject is still eligible for study)
Descrizione

subject has a clinical diagnosis of acute myocardial infarction

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0155626
subject has a pulmonary embolism (pe) on admission
Descrizione

subject has a pulmonary embolism

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0034065
subject is dialysis dependent
Descrizione

subject is dialysis dependent

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0011946
subject has a cardiac resynchronization device (crt) which has been re-programmed at any time during the study
Descrizione

subject has a cardiac resynchronization device

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1135479
subject has chronic obstructive pulmonary disease (copd) who is oxygen or steroid dependent
Descrizione

chronic obstructive pulmonary disease (copd) who is oxygen or steroid dependent

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0742814
UMLS CUI [1,2]
C0184633
subject has severe hypertension > 180 millimeter of mercury (mmhg) resting systolic at time of test
Descrizione

subject has severe hypertension

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0020538
subject has severe heart failure with renal insufficiency (with creatinine clearance rate (crcl) of 30 or less) and/or on iv inotropic therapy and/or enrolling in hospice
Descrizione

severe heart failure with renal insufficiency

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0494576
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Similar models

Eligibility Acute Decompensated Heart Failure NCT01960218

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
subject is 18 years and older
boolean
C0001779 (UMLS CUI [1])
hospitalized for acute decompensated heart failure
Item
subject is hospitalized for acute decompensated heart failure (adhf)
boolean
C1609524 (UMLS CUI [1])
C0019993 (UMLS CUI [2])
subject is stage c:class ii/iii/iv systolic or diastolic heart failure
Item
subject is stage c:class ii/iii/iv systolic or diastolic heart failure
boolean
C3531729 (UMLS CUI [1])
C3531731 (UMLS CUI [2])
informed consent
Item
subject is willing and to provide appropriate informed consent
boolean
C0021430 (UMLS CUI [1])
compliance behavior
Item
subject is willing and able to comply with the requirements of the protocol, including follow-up evaluations and schedule
boolean
C1321605 (UMLS CUI [1])
compliance behavior
Item
subject is willing to use the shape-hf cardiopulmonary exercise testing system
boolean
C1321605 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Pregnancy
Item
the subject is pregnant (verified in a manner consistent with institution's standard of care)
boolean
C0549206 (UMLS CUI [1])
currently participating in another investigational device or drug trial
Item
subject is currently participating in another investigational device or drug trial
boolean
C2348568 (UMLS CUI [1])
subject is a prisoner, a minor or unable to adequately give informed consent
Item
subject is a prisoner, a minor or unable to adequately give informed consent due to mental or physical condition
boolean
C0021430 (UMLS CUI [1])
C0439801 (UMLS CUI [2])
C0009488 (UMLS CUI [3])
subject is unwilling or unable to return for the required follow-up
Item
subject is unwilling or unable to return for the required follow-up after test
boolean
C1321605 (UMLS CUI [1])
left ventricular assist device
Item
subject has left ventricular assist device (lvad)
boolean
C0181598 (UMLS CUI [1])
listed for transplant
Item
subject is listed for transplant
boolean
C0040732 (UMLS CUI [1])
subject has a clinical diagnosis of acute myocardial infarction
Item
subject has a clinical diagnosis of acute myocardial infarction (ami) on admission (note: if troponin measurements have been collected and are elevated but not due to an mi subject is still eligible for study)
boolean
C0155626 (UMLS CUI [1])
subject has a pulmonary embolism
Item
subject has a pulmonary embolism (pe) on admission
boolean
C0034065 (UMLS CUI [1])
subject is dialysis dependent
Item
subject is dialysis dependent
boolean
C0011946 (UMLS CUI [1])
subject has a cardiac resynchronization device
Item
subject has a cardiac resynchronization device (crt) which has been re-programmed at any time during the study
boolean
C1135479 (UMLS CUI [1])
chronic obstructive pulmonary disease (copd) who is oxygen or steroid dependent
Item
subject has chronic obstructive pulmonary disease (copd) who is oxygen or steroid dependent
boolean
C0742814 (UMLS CUI [1,1])
C0184633 (UMLS CUI [1,2])
subject has severe hypertension
Item
subject has severe hypertension > 180 millimeter of mercury (mmhg) resting systolic at time of test
boolean
C0020538 (UMLS CUI [1])
severe heart failure with renal insufficiency
Item
subject has severe heart failure with renal insufficiency (with creatinine clearance rate (crcl) of 30 or less) and/or on iv inotropic therapy and/or enrolling in hospice
boolean
C0494576 (UMLS CUI [1])
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