ID

35939

Descripción

Clinical Assessment of the Treatment With Cardiac Sympathetic Blockade on Chronic Heart Failure; ODM derived from: https://clinicaltrials.gov/show/NCT02391142

Link

https://clinicaltrials.gov/show/NCT02391142

Palabras clave

Versiones (1)
  1. 5/4/19 5/4/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

5 de abril de 2019

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Heart Failure NCT02391142

Inglés

Eligibility Heart Failure NCT02391142

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
20-70 years old
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
more than 3 months of chronic heart failure history or clinical symptoms of heart failure last for more than 3 months (including acute episode of chronic heart failure), chronic heart failure diagnostic criteria refer to 2012esc guidelines for the diagnosis and treatment of acute and chronic heart failure
Descripción

Chronic heart failure Disease length | Symptoms Heart failure | Episode of Chronic heart failure

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0264716
UMLS CUI [1,2]
C0872146
UMLS CUI [2,1]
C1457887
UMLS CUI [2,2]
C0018801
UMLS CUI [3,1]
C0332189
UMLS CUI [3,2]
C0264716
nyha functional class iii-iv, ejection fraction ≤45%
Descripción

New York Heart Association Classification | Cardiac ejection fraction

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1275491
UMLS CUI [2]
C0232174
nt-probnp>400ng/l
Descripción

N-Terminal ProB-type Natriuretic Peptide Measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3272900
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
first episode of acute heart failure
Descripción

First episode Heart failure

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0439615
UMLS CUI [1,2]
C0018801
unrepaired valvular heart disease accompanied with hemodynamic changes
Descripción

Heart valve disease | Resolution Lacking | Change Hemodynamic

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0018824
UMLS CUI [2,1]
C1514893
UMLS CUI [2,2]
C0332268
UMLS CUI [3,1]
C0392747
UMLS CUI [3,2]
C0019010
hypertrophic cardiomyopathy, pericardial disease, congenital heart disease, severe pulmonary hypertension
Descripción

Hypertrophic Cardiomyopathy | Disorder of pericardium | Congenital heart disease | Pulmonary Hypertension Severe

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0007194
UMLS CUI [2]
C0265122
UMLS CUI [3]
C0152021
UMLS CUI [4,1]
C0020542
UMLS CUI [4,2]
C0205082
second-degree type 2 or worse sinoatrial or atrioventricular block without pacemaker therapy
Descripción

Second degree sinoatrial block Type | Second degree atrioventricular block | Pacemaker Procedure Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3854674
UMLS CUI [1,2]
C0332307
UMLS CUI [2]
C0264906
UMLS CUI [3,1]
C3275122
UMLS CUI [3,2]
C0332197
right heart failure caused by various diseases, respiratory failure or right heart failure induced by chronic obstructive pulmonary disease
Descripción

Right-Sided Heart Failure caused by Disease | Respiratory Failure | Right-Sided Heart Failure Chronic Obstructive Airway Disease Induced

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0235527
UMLS CUI [1,2]
C0015127
UMLS CUI [1,3]
C0012634
UMLS CUI [2]
C1145670
UMLS CUI [3,1]
C0235527
UMLS CUI [3,2]
C0024117
UMLS CUI [3,3]
C0205263
overt renal decompensation: serum creatinine＞2.1mg/dl(186umol/l)
Descripción

Renal decompensation | Creatinine measurement, serum

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0748288
UMLS CUI [2]
C0201976
severe hepatic dysfunction, transaminase or alkaline phosphatase > 3 times the upper limit of normal
Descripción

Liver Dysfunction Severe | Transaminases increased | Alkaline phosphatase raised

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0086565
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C0438717
UMLS CUI [3]
C0151849
cerebral vascular accident in three months( cerebral infarction, cerebral embolism, cerebral hemorrhage,etc)
Descripción

Cerebrovascular accident | Cerebral Infarction | Cerebral Embolism | Cerebral Hemorrhage

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0038454
UMLS CUI [2]
C0007785
UMLS CUI [3]
C0007780
UMLS CUI [4]
C2937358
life expectancy shorter than 6 months
Descripción

Life Expectancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023671
patients with a previous or present history of tumour or precancerous lesions confirmed by pathological examination
Descripción

Malignant Neoplasms | Precancerous lesions

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2]
C0940937
spine deformity or skin infection at puncture site
Descripción

Deformity of spine Puncture Site | Skin infection Puncture Site

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0575157
UMLS CUI [1,2]
C0034117
UMLS CUI [1,3]
C1515974
UMLS CUI [2,1]
C0037278
UMLS CUI [2,2]
C0034117
UMLS CUI [2,3]
C1515974
participate in any clinical drug trials in the three months
Descripción

Study Subject Participation Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
the patients who do not sign the informed consent, unable or unwilling to comply with the requirements of the protocol or unsuitable for the study
Descripción

Informed Consent Absent | Protocol Compliance Unable | Protocol Compliance Unwilling | Study Subject Participation Status Inappropriate

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0525058
UMLS CUI [2,2]
C1299582
UMLS CUI [3,1]
C0525058
UMLS CUI [3,2]
C0558080
UMLS CUI [4,1]
C2348568
UMLS CUI [4,2]
C1548788
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Similar models

Eligibility Heart Failure NCT02391142

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
20-70 years old
boolean
C0001779 (UMLS CUI [1])
Chronic heart failure Disease length | Symptoms Heart failure | Episode of Chronic heart failure
Item
more than 3 months of chronic heart failure history or clinical symptoms of heart failure last for more than 3 months (including acute episode of chronic heart failure), chronic heart failure diagnostic criteria refer to 2012esc guidelines for the diagnosis and treatment of acute and chronic heart failure
boolean
C0264716 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
C1457887 (UMLS CUI [2,1])
C0018801 (UMLS CUI [2,2])
C0332189 (UMLS CUI [3,1])
C0264716 (UMLS CUI [3,2])
New York Heart Association Classification | Cardiac ejection fraction
Item
nyha functional class iii-iv, ejection fraction ≤45%
boolean
C1275491 (UMLS CUI [1])
C0232174 (UMLS CUI [2])
N-Terminal ProB-type Natriuretic Peptide Measurement
Item
nt-probnp>400ng/l
boolean
C3272900 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
First episode Heart failure
Item
first episode of acute heart failure
boolean
C0439615 (UMLS CUI [1,1])
C0018801 (UMLS CUI [1,2])
Heart valve disease | Resolution Lacking | Change Hemodynamic
Item
unrepaired valvular heart disease accompanied with hemodynamic changes
boolean
C0018824 (UMLS CUI [1])
C1514893 (UMLS CUI [2,1])
C0332268 (UMLS CUI [2,2])
C0392747 (UMLS CUI [3,1])
C0019010 (UMLS CUI [3,2])
Hypertrophic Cardiomyopathy | Disorder of pericardium | Congenital heart disease | Pulmonary Hypertension Severe
Item
hypertrophic cardiomyopathy, pericardial disease, congenital heart disease, severe pulmonary hypertension
boolean
C0007194 (UMLS CUI [1])
C0265122 (UMLS CUI [2])
C0152021 (UMLS CUI [3])
C0020542 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
Second degree sinoatrial block Type | Second degree atrioventricular block | Pacemaker Procedure Absent
Item
second-degree type 2 or worse sinoatrial or atrioventricular block without pacemaker therapy
boolean
C3854674 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
C0264906 (UMLS CUI [2])
C3275122 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
Right-Sided Heart Failure caused by Disease | Respiratory Failure | Right-Sided Heart Failure Chronic Obstructive Airway Disease Induced
Item
right heart failure caused by various diseases, respiratory failure or right heart failure induced by chronic obstructive pulmonary disease
boolean
C0235527 (UMLS CUI [1,1])
C0015127 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,3])
C1145670 (UMLS CUI [2])
C0235527 (UMLS CUI [3,1])
C0024117 (UMLS CUI [3,2])
C0205263 (UMLS CUI [3,3])
Renal decompensation | Creatinine measurement, serum
Item
overt renal decompensation: serum creatinine＞2.1mg/dl(186umol/l)
boolean
C0748288 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
Liver Dysfunction Severe | Transaminases increased | Alkaline phosphatase raised
Item
severe hepatic dysfunction, transaminase or alkaline phosphatase > 3 times the upper limit of normal
boolean
C0086565 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0438717 (UMLS CUI [2])
C0151849 (UMLS CUI [3])
Cerebrovascular accident | Cerebral Infarction | Cerebral Embolism | Cerebral Hemorrhage
Item
cerebral vascular accident in three months( cerebral infarction, cerebral embolism, cerebral hemorrhage,etc)
boolean
C0038454 (UMLS CUI [1])
C0007785 (UMLS CUI [2])
C0007780 (UMLS CUI [3])
C2937358 (UMLS CUI [4])
Life Expectancy
Item
life expectancy shorter than 6 months
boolean
C0023671 (UMLS CUI [1])
Malignant Neoplasms | Precancerous lesions
Item
patients with a previous or present history of tumour or precancerous lesions confirmed by pathological examination
boolean
C0006826 (UMLS CUI [1])
C0940937 (UMLS CUI [2])
Deformity of spine Puncture Site | Skin infection Puncture Site
Item
spine deformity or skin infection at puncture site
boolean
C0575157 (UMLS CUI [1,1])
C0034117 (UMLS CUI [1,2])
C1515974 (UMLS CUI [1,3])
C0037278 (UMLS CUI [2,1])
C0034117 (UMLS CUI [2,2])
C1515974 (UMLS CUI [2,3])
Study Subject Participation Status
Item
participate in any clinical drug trials in the three months
boolean
C2348568 (UMLS CUI [1])
Informed Consent Absent | Protocol Compliance Unable | Protocol Compliance Unwilling | Study Subject Participation Status Inappropriate
Item
the patients who do not sign the informed consent, unable or unwilling to comply with the requirements of the protocol or unsuitable for the study
boolean
C0021430 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
C0525058 (UMLS CUI [3,1])
C0558080 (UMLS CUI [3,2])
C2348568 (UMLS CUI [4,1])
C1548788 (UMLS CUI [4,2])
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