ID

12596

Descripción

Sequential Cystatin C Levels and Renal Impairment in Acute Heart Failure; ODM derived from: https://clinicaltrials.gov/show/NCT00561483

Link

https://clinicaltrials.gov/show/NCT00561483

Palabras clave

  1. 3/12/15 3/12/15 -
Subido en

3 de diciembre de 2015

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Acute Heart Failure NCT00561483

Eligibility Acute Heart Failure NCT00561483

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
hospital admission within 48 hours for adhf, with an expected stay over 24 hours.
Descripción

hospital admission within 48 hours for adhf, with an expected stay over 24 hours

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1609524
UMLS CUI [1,2]
C0019993
evidence of fluid overload, including jugular venous distention, pulmonary rales, peripheral edema, and/or ascites receiving diuretic therapy
Descripción

evidence of fluid overload, including jugular venous distention, pulmonary rales, peripheral edema, and/or ascites receiving diuretic therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0546817
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
heart failure due to congenital heart disease or critical aortic stenosis (potentially different cardio-renal pathophysiology)
Descripción

heart failure due to congenital heart disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3532229
acute myocardial infarction or unstable acute coronary syndromes
Descripción

acute myocardial infarction

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0155626
end-stage renal insufficiency on renal replacement therapy (already has underlying advanced renal failure).
Descripción

end-stage renal insufficiency

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2709206
patients with active cancer (cystatin c has been shown to be produced by some tumors)
Descripción

patients with active cancer

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006826
known exposure to nephrotoxic agents (such as contrast dye) or planned surgery during hospitalization at the time of enrollment
Descripción

known exposure to nephrotoxic agents (such as contrast dye) or planned surgery during hospitalization at the time of enrollment

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0742799
UMLS CUI [2]
C0543467
hemoglobin < 9 mg/dl or clinically significant active bleeding.
Descripción

hemoglobin < 9 mg/dl or clinically significant active bleeding.

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0019080
UMLS CUI [2]
C0002871
unable to comply with protocol or unable to have informed consent
Descripción

Compliance behavior

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1321605

Similar models

Eligibility Acute Heart Failure NCT00561483

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
hospital admission within 48 hours for adhf, with an expected stay over 24 hours
Item
hospital admission within 48 hours for adhf, with an expected stay over 24 hours.
boolean
C1609524 (UMLS CUI [1,1])
C0019993 (UMLS CUI [1,2])
evidence of fluid overload, including jugular venous distention, pulmonary rales, peripheral edema, and/or ascites receiving diuretic therapy
Item
evidence of fluid overload, including jugular venous distention, pulmonary rales, peripheral edema, and/or ascites receiving diuretic therapy
boolean
C0546817 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
heart failure due to congenital heart disease
Item
heart failure due to congenital heart disease or critical aortic stenosis (potentially different cardio-renal pathophysiology)
boolean
C3532229 (UMLS CUI [1])
acute myocardial infarction
Item
acute myocardial infarction or unstable acute coronary syndromes
boolean
C0155626 (UMLS CUI [1])
end-stage renal insufficiency
Item
end-stage renal insufficiency on renal replacement therapy (already has underlying advanced renal failure).
boolean
C2709206 (UMLS CUI [1])
patients with active cancer
Item
patients with active cancer (cystatin c has been shown to be produced by some tumors)
boolean
C0006826 (UMLS CUI [1])
known exposure to nephrotoxic agents (such as contrast dye) or planned surgery during hospitalization at the time of enrollment
Item
known exposure to nephrotoxic agents (such as contrast dye) or planned surgery during hospitalization at the time of enrollment
boolean
C0742799 (UMLS CUI [1])
C0543467 (UMLS CUI [2])
hemoglobin < 9 mg/dl or clinically significant active bleeding.
Item
hemoglobin < 9 mg/dl or clinically significant active bleeding.
boolean
C0019080 (UMLS CUI [1])
C0002871 (UMLS CUI [2])
Compliance behavior
Item
unable to comply with protocol or unable to have informed consent
boolean
C1321605 (UMLS CUI [1])

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