ID

39449

Descripción

Renal Sympathetic Modification in Patients With Heart Failure; ODM derived from: https://clinicaltrials.gov/show/NCT01402726

Link

https://clinicaltrials.gov/show/NCT01402726

Palabras clave

  1. 11/1/20 11/1/20 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

11 de enero de 2020

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Heart Failure NCT01402726

Eligibility Heart Failure NCT01402726

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
≥ 18 years old, and ≤ 75 years old of age
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
more than half a year history of heart failure, except for valvular heart disease
Descripción

Heart failure Disease length | Exception Heart valve disease

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C0872146
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0018824
heart failure patients nyha class ii iii iv
Descripción

Heart failure New York Heart Association Classification

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1275491
left ventricular ejection function ≤ 40% or ≥ 45% (that is heart failure with preserved ejection fraction) with simpson's method
Descripción

Left ventricular ejection fraction | Heart failure with preserved ejection fraction

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0428772
UMLS CUI [2]
C4509226
estimated glomerular filtration rate (egfr) of ≥ 45ml/min
Descripción

Estimated Glomerular Filtration Rate

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3811844
is competent and willing to provide written, informed consent to participate in this clinical study
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with acute heart failure
Descripción

Acute heart failure

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0264714
patients with acute coronary syndrome
Descripción

Acute Coronary Syndrome

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0948089
estimated glomerular filtration rate (egfr) of < 45ml/min
Descripción

Estimated Glomerular Filtration Rate

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3811844
has the history of renal restenosis or renal stents implantation
Descripción

Restenosis renal artery | Insertion of renal artery stent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0333186
UMLS CUI [1,2]
C0035065
UMLS CUI [2]
C1532969
has experienced ami (old myocardial infarction is not excluded), unstable angina pectoris, cerebrovascular accidents, and alimentary tract hemorrhage within 3 months
Descripción

Acute myocardial infarction | Angina, Unstable | Cerebrovascular accident | Gastrointestinal Hemorrhage

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0155626
UMLS CUI [2]
C0002965
UMLS CUI [3]
C0038454
UMLS CUI [4]
C0017181
patients with sick sinus syndrome
Descripción

Sick Sinus Syndrome

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0037052
pregnant women
Descripción

Pregnancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
mental disorders
Descripción

Mental disorders

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004936
patients that have allergy to contrast agent
Descripción

Contrast media allergy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0570562
patients that do not go with follow-up
Descripción

Compliance behavior Lacking Follow-up

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0332268
UMLS CUI [1,3]
C3274571
others such as researcher considers it is not appropriate to be included into the study
Descripción

Study Subject Participation Status Inappropriate

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C1548788

Similar models

Eligibility Heart Failure NCT01402726

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
≥ 18 years old, and ≤ 75 years old of age
boolean
C0001779 (UMLS CUI [1])
Heart failure Disease length | Exception Heart valve disease
Item
more than half a year history of heart failure, except for valvular heart disease
boolean
C0018801 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0018824 (UMLS CUI [2,2])
Heart failure New York Heart Association Classification
Item
heart failure patients nyha class ii iii iv
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
Left ventricular ejection fraction | Heart failure with preserved ejection fraction
Item
left ventricular ejection function ≤ 40% or ≥ 45% (that is heart failure with preserved ejection fraction) with simpson's method
boolean
C0428772 (UMLS CUI [1])
C4509226 (UMLS CUI [2])
Estimated Glomerular Filtration Rate
Item
estimated glomerular filtration rate (egfr) of ≥ 45ml/min
boolean
C3811844 (UMLS CUI [1])
Informed Consent
Item
is competent and willing to provide written, informed consent to participate in this clinical study
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Acute heart failure
Item
patients with acute heart failure
boolean
C0264714 (UMLS CUI [1])
Acute Coronary Syndrome
Item
patients with acute coronary syndrome
boolean
C0948089 (UMLS CUI [1])
Estimated Glomerular Filtration Rate
Item
estimated glomerular filtration rate (egfr) of < 45ml/min
boolean
C3811844 (UMLS CUI [1])
Restenosis renal artery | Insertion of renal artery stent
Item
has the history of renal restenosis or renal stents implantation
boolean
C0333186 (UMLS CUI [1,1])
C0035065 (UMLS CUI [1,2])
C1532969 (UMLS CUI [2])
Acute myocardial infarction | Angina, Unstable | Cerebrovascular accident | Gastrointestinal Hemorrhage
Item
has experienced ami (old myocardial infarction is not excluded), unstable angina pectoris, cerebrovascular accidents, and alimentary tract hemorrhage within 3 months
boolean
C0155626 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
C0017181 (UMLS CUI [4])
Sick Sinus Syndrome
Item
patients with sick sinus syndrome
boolean
C0037052 (UMLS CUI [1])
Pregnancy
Item
pregnant women
boolean
C0032961 (UMLS CUI [1])
Mental disorders
Item
mental disorders
boolean
C0004936 (UMLS CUI [1])
Contrast media allergy
Item
patients that have allergy to contrast agent
boolean
C0570562 (UMLS CUI [1])
Compliance behavior Lacking Follow-up
Item
patients that do not go with follow-up
boolean
C1321605 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
C3274571 (UMLS CUI [1,3])
Study Subject Participation Status Inappropriate
Item
others such as researcher considers it is not appropriate to be included into the study
boolean
C2348568 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])

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