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ID
13622
Beschrijving
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
Trefwoorden
Versies (1)
- 21-02-16 21-02-16 -
Geüploaded op
21 februari 2016
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Heart Failure, Congestive NCT00288730
Eligibility Heart Failure, Congestive NCT00288730
- StudyEvent: Eligibility
Similar models
Eligibility Heart Failure, Congestive NCT00288730
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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])
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])
C0871470 (UMLS CUI [2])
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])
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])
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])
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])
C1321605 (UMLS CUI [2])