ID

13622

Description

A Study of Two Doses of Intravenous NATRECOR hBNP (Nesiritide) in Patients With Worsening Congestive Heart Failure Who Have Difficulty Breathing at Rest; ODM derived from: https://clinicaltrials.gov/show/NCT00288730

Link

https://clinicaltrials.gov/show/NCT00288730

Keywords

Versions (1)
  1. 2/21/16 2/21/16 -
Uploaded on

February 21, 2016

DOI

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License

Creative Commons BY 4.0
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Eligibility Heart Failure, Congestive NCT00288730

English

Eligibility Heart Failure, Congestive NCT00288730

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
history of chronic congestive heart failure (chf)
Description

chronic congestive heart failure

Data type

boolean

Alias
UMLS CUI [1]
C0264722
symptomatic, decompensated chf for which intravenous therapy is deemed appropriate for the hospitalized patient
Description

chf decompensated, hospitalized patient with indication for intravenous therapy

Data type

boolean

Alias
UMLS CUI [1,1]
C0264722
UMLS CUI [1,2]
C0205434
UMLS CUI [2]
C0019993
UMLS CUI [3,1]
C0455142
UMLS CUI [3,2]
C1444656
documentation of pulmonary capillary wedge pressure (pcwp) >= 18 mm hg, cl <= 2.7 ml/min/m² and systolic blood pressure >= 90 mm hg with consistent baseline hemodynamic measurements.
Description

pulmonary capillary wedge pressure, systolic blood pressure

Data type

boolean

Alias
UMLS CUI [1]
C0086879
UMLS CUI [2]
C0871470
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
had a myocardial infarction within the previous 48 hours or unstable angina
Description

myocardial infarction or unstable angina

Data type

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0002965
stroke within the previous 3 months or other evidence of significantly compromised central nervous system perfusion
Description

stroke or ompromised central nervous system perfusion

Data type

boolean

Alias
UMLS CUI [1]
C0038454
UMLS CUI [2]
C0851452
has significant valvular stenosis hypertrophic, restrictive or obstructive cardiomyopathy, constrictive pericarditis, primary pulmonary hypertension, biopsy-proven active myocarditis, or complex congenital heart disease
Description

comorbidity, heart or lung diseases

Data type

boolean

Alias
UMLS CUI [1]
C0009488
UMLS CUI [2]
C0018799
UMLS CUI [3]
C0024115
receiving ongoing treatment with an intravenous vasostrictive agent for this episode of decompressed chf that could not be discontinued for an appropriate washout period to permit the reassessment of baseline hemodynamic and clinical status prior to initiating drug study
Description

treatment with an intravenous vasostrictive agent that could not be discontinued for assessment

Data type

boolean

Alias
UMLS CUI [1]
C1321605
clinical status so unstable that the subject can not tolerate placement of a swan-ganz catheter.
Description

clinical status too unstable for swan-ganz catheter

Data type

boolean

Alias
UMLS CUI [1]
C0449440
UMLS CUI [2]
C1321605
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Similar models

Eligibility Heart Failure, Congestive NCT00288730

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
chronic congestive heart failure
Item
history of chronic congestive heart failure (chf)
boolean
C0264722 (UMLS CUI [1])
chf decompensated, hospitalized patient with indication for intravenous therapy
Item
symptomatic, decompensated chf for which intravenous therapy is deemed appropriate for the hospitalized patient
boolean
C0264722 (UMLS CUI [1,1])
C0205434 (UMLS CUI [1,2])
C0019993 (UMLS CUI [2])
C0455142 (UMLS CUI [3,1])
C1444656 (UMLS CUI [3,2])
pulmonary capillary wedge pressure, systolic blood pressure
Item
documentation of pulmonary capillary wedge pressure (pcwp) >= 18 mm hg, cl <= 2.7 ml/min/m² and systolic blood pressure >= 90 mm hg with consistent baseline hemodynamic measurements.
boolean
C0086879 (UMLS CUI [1])
C0871470 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
myocardial infarction or unstable angina
Item
had a myocardial infarction within the previous 48 hours or unstable angina
boolean
C0027051 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
stroke or ompromised central nervous system perfusion
Item
stroke within the previous 3 months or other evidence of significantly compromised central nervous system perfusion
boolean
C0038454 (UMLS CUI [1])
C0851452 (UMLS CUI [2])
comorbidity, heart or lung diseases
Item
has significant valvular stenosis hypertrophic, restrictive or obstructive cardiomyopathy, constrictive pericarditis, primary pulmonary hypertension, biopsy-proven active myocarditis, or complex congenital heart disease
boolean
C0009488 (UMLS CUI [1])
C0018799 (UMLS CUI [2])
C0024115 (UMLS CUI [3])
treatment with an intravenous vasostrictive agent that could not be discontinued for assessment
Item
receiving ongoing treatment with an intravenous vasostrictive agent for this episode of decompressed chf that could not be discontinued for an appropriate washout period to permit the reassessment of baseline hemodynamic and clinical status prior to initiating drug study
boolean
C1321605 (UMLS CUI [1])
clinical status too unstable for swan-ganz catheter
Item
clinical status so unstable that the subject can not tolerate placement of a swan-ganz catheter.
boolean
C0449440 (UMLS CUI [1])
C1321605 (UMLS CUI [2])
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