ID

12582

Descrição

Assessment of Biomarkers and Cardiorenal Syndrome in Acute Decompensated Heart Failure With Vasodilator Therapy; ODM derived from: https://clinicaltrials.gov/show/NCT00842023

Link

https://clinicaltrials.gov/show/NCT00842023

Palavras-chave

  1. 03/12/2015 03/12/2015 -
Transferido a

3 de dezembro de 2015

DOI

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Licença

Creative Commons BY 4.0

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Eligibility Acute Decompensated Heart Failure NCT00842023

Eligibility Acute Decompensated Heart Failure NCT00842023

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
at least 18 years of age.
Descrição

Age

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0001779
subject must be able to understand the potential risks and benefits associated with the study.
Descrição

subject must be able to understand the potential risks and benefits

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0021430
baseline systolic blood pressure ≥ 90 mm hg at the time of enrollment.
Descrição

systolic blood pressure

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0871470
clinical symptoms of dyspnea and laboratory admission bnp levels > 500 pg/ml.
Descrição

clinical symptoms of dyspnea and laboratory admission bnp levels > 500 pg/ml

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0013404
UMLS CUI [2]
C1095989
neither pregnant or breastfeeding at the time of enrollment.
Descrição

pregnant or breastfeeding

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
authorization of patient's enrollment by patient's medical provider.
Descrição

medical provider authorization

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0680281
UMLS CUI [1,2]
C0018724
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
younger than 18 years of age
Descrição

younger than 18 years of age

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0001779
denies written informed consent
Descrição

denies informed consent

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0021430
pregnant or lactating.
Descrição

pregnant or lactating

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
baseline systolic bp < 90 mmhg or cardiogenic shock
Descrição

baseline systolic bp < 90 mmhg or cardiogenic shock

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0036980
UMLS CUI [2]
C0871470
no symptoms of congestion or admission bnp < 500 pg/ml
Descrição

no symptoms of congestion or admission bnp < 500 pg/ml

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0700148
UMLS CUI [2]
C1095989
known allergy to e.coli-derived products, or any history of anaphylactic reactions to nesiritide.
Descrição

allergy to e.coli-derived products, or any history of anaphylactic reactions to nesiritide

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0020517
UMLS CUI [2]
C0054015
receiving dialysis at the time of enrollment.
Descrição

receiving dialysis at the time of enrollment

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0011946
serum creatinine > 2.5 mg/dl at the time of enrollment.
Descrição

serum creatinine > 2.5 mg/dl at the time of enrollment

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0201976

Similar models

Eligibility Acute Decompensated Heart Failure NCT00842023

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
at least 18 years of age.
boolean
C0001779 (UMLS CUI [1])
subject must be able to understand the potential risks and benefits
Item
subject must be able to understand the potential risks and benefits associated with the study.
boolean
C0021430 (UMLS CUI [1])
systolic blood pressure
Item
baseline systolic blood pressure ≥ 90 mm hg at the time of enrollment.
boolean
C0871470 (UMLS CUI [1])
clinical symptoms of dyspnea and laboratory admission bnp levels > 500 pg/ml
Item
clinical symptoms of dyspnea and laboratory admission bnp levels > 500 pg/ml.
boolean
C0013404 (UMLS CUI [1])
C1095989 (UMLS CUI [2])
pregnant or breastfeeding
Item
neither pregnant or breastfeeding at the time of enrollment.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
medical provider authorization
Item
authorization of patient's enrollment by patient's medical provider.
boolean
C0680281 (UMLS CUI [1,1])
C0018724 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
younger than 18 years of age
Item
younger than 18 years of age
boolean
C0001779 (UMLS CUI [1])
denies informed consent
Item
denies written informed consent
boolean
C0021430 (UMLS CUI [1])
pregnant or lactating
Item
pregnant or lactating.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
baseline systolic bp < 90 mmhg or cardiogenic shock
Item
baseline systolic bp < 90 mmhg or cardiogenic shock
boolean
C0036980 (UMLS CUI [1])
C0871470 (UMLS CUI [2])
no symptoms of congestion or admission bnp < 500 pg/ml
Item
no symptoms of congestion or admission bnp < 500 pg/ml
boolean
C0700148 (UMLS CUI [1])
C1095989 (UMLS CUI [2])
allergy to e.coli-derived products, or any history of anaphylactic reactions to nesiritide
Item
known allergy to e.coli-derived products, or any history of anaphylactic reactions to nesiritide.
boolean
C0020517 (UMLS CUI [1])
C0054015 (UMLS CUI [2])
receiving dialysis at the time of enrollment
Item
receiving dialysis at the time of enrollment.
boolean
C0011946 (UMLS CUI [1])
serum creatinine > 2.5 mg/dl at the time of enrollment
Item
serum creatinine > 2.5 mg/dl at the time of enrollment.
boolean
C0201976 (UMLS CUI [1])

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