ID

12587

Beschrijving

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

Link

https://clinicaltrials.gov/show/NCT01960218

Trefwoorden

Versies (1)
  1. 03-12-15 03-12-15 -
Geüploaded op

3 december 2015

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Acute Decompensated Heart Failure NCT01960218

Engels

Eligibility Acute Decompensated Heart Failure NCT01960218

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
subject is 18 years and older
Beschrijving

Age

Datatype

boolean

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

hospitalized for acute decompensated heart failure

Datatype

boolean

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

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

Datatype

boolean

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

informed consent

Datatype

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
Beschrijving

compliance behavior

Datatype

boolean

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

compliance behavior

Datatype

boolean

Alias
UMLS CUI [1]
C1321605
Exclusion Criteria
Beschrijving

Exclusion Criteria

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

Pregnancy

Datatype

boolean

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

currently participating in another investigational device or drug trial

Datatype

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
Beschrijving

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

Datatype

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
Beschrijving

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

Datatype

boolean

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

left ventricular assist device

Datatype

boolean

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

listed for transplant

Datatype

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)
Beschrijving

subject has a clinical diagnosis of acute myocardial infarction

Datatype

boolean

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

subject has a pulmonary embolism

Datatype

boolean

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

subject is dialysis dependent

Datatype

boolean

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

subject has a cardiac resynchronization device

Datatype

boolean

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

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

Datatype

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
Beschrijving

subject has severe hypertension

Datatype

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
Beschrijving

severe heart failure with renal insufficiency

Datatype

boolean

Alias
UMLS CUI [1]
C0494576
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Similar models

Eligibility Acute Decompensated Heart Failure NCT01960218

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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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