ID

39398

Descripción

Investigating the Inotropic Potential of Apelin; ODM derived from: https://clinicaltrials.gov/show/NCT01179061

Link

https://clinicaltrials.gov/show/NCT01179061

Palabras clave

Versiones (1)
  1. 7/1/20 7/1/20 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

7 de enero de 2020

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Heart Failure NCT01179061

Inglés

Eligibility Heart Failure NCT01179061

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
healthy volunteers:
Descripción

Healthy Volunteers

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1708335
>18yrs
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
heart failure patients;
Descripción

Heart failure Patients

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C0030705
new york heart failure class ii-iv
Descripción

Heart failure New York Heart Association Classification

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1275491
ejection fractional <35% or fractional shortening <20% within previous 6months.
Descripción

Left ventricular ejection fraction | Left Ventricular Fractional Shortening

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0428772
UMLS CUI [2]
C1335957
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
all subjects,
Descripción

Study Subject All

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0681850
UMLS CUI [1,2]
C0444868
females of child bearing age not on adequate contraception
Descripción

Childbearing Potential Contraceptive methods Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0700589
UMLS CUI [1,3]
C0332197
lack of informed consent
Descripción

Informed Consent Lacking

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0332268
age <18yrs
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
current involvement in any other research study
Descripción

Study Subject Participation Status | Research study

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0681814
systolic bp >190 or <100
Descripción

Systolic Pressure

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0871470
malignant arrhythmias
Descripción

Cardiac Arrhythmia Serious

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0003811
UMLS CUI [1,2]
C0205404
renal or hepatic failure
Descripción

Kidney Failure | Liver Failure

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0035078
UMLS CUI [2]
C0085605
haemodynamically significant aortic stenosis
Descripción

Aortic Stenosis Hemodynamic Significant

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0003507
UMLS CUI [1,2]
C0019010
UMLS CUI [1,3]
C0750502
severe or significant co-morbidity
Descripción

Comorbidity Severe | Comorbidity Significant

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C0009488
UMLS CUI [2,2]
C0750502
pacemakers
Descripción

Artificial cardiac pacemaker

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0030163
healthy volunteers
Descripción

Healthy Volunteers

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1708335
any regular medication
Descripción

Pharmaceutical Preparations Regular

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0205272
previous history of any cardiovascular disease
Descripción

Cardiovascular Disease Previous

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0007222
UMLS CUI [1,2]
C0205156
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Similar models

Eligibility Heart Failure NCT01179061

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Healthy Volunteers
Item
healthy volunteers:
boolean
C1708335 (UMLS CUI [1])
Age
Item
>18yrs
boolean
C0001779 (UMLS CUI [1])
Heart failure Patients
Item
heart failure patients;
boolean
C0018801 (UMLS CUI [1,1])
C0030705 (UMLS CUI [1,2])
Heart failure New York Heart Association Classification
Item
new york heart failure class ii-iv
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
Left ventricular ejection fraction | Left Ventricular Fractional Shortening
Item
ejection fractional <35% or fractional shortening <20% within previous 6months.
boolean
C0428772 (UMLS CUI [1])
C1335957 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Study Subject All
Item
all subjects,
boolean
C0681850 (UMLS CUI [1,1])
C0444868 (UMLS CUI [1,2])
Childbearing Potential Contraceptive methods Absent
Item
females of child bearing age not on adequate contraception
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Informed Consent Lacking
Item
lack of informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
Age
Item
age <18yrs
boolean
C0001779 (UMLS CUI [1])
Study Subject Participation Status | Research study
Item
current involvement in any other research study
boolean
C2348568 (UMLS CUI [1])
C0681814 (UMLS CUI [2])
Systolic Pressure
Item
systolic bp >190 or <100
boolean
C0871470 (UMLS CUI [1])
Cardiac Arrhythmia Serious
Item
malignant arrhythmias
boolean
C0003811 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
Kidney Failure | Liver Failure
Item
renal or hepatic failure
boolean
C0035078 (UMLS CUI [1])
C0085605 (UMLS CUI [2])
Aortic Stenosis Hemodynamic Significant
Item
haemodynamically significant aortic stenosis
boolean
C0003507 (UMLS CUI [1,1])
C0019010 (UMLS CUI [1,2])
C0750502 (UMLS CUI [1,3])
Comorbidity Severe | Comorbidity Significant
Item
severe or significant co-morbidity
boolean
C0009488 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0009488 (UMLS CUI [2,1])
C0750502 (UMLS CUI [2,2])
Artificial cardiac pacemaker
Item
pacemakers
boolean
C0030163 (UMLS CUI [1])
Healthy Volunteers
Item
healthy volunteers
boolean
C1708335 (UMLS CUI [1])
Pharmaceutical Preparations Regular
Item
any regular medication
boolean
C0013227 (UMLS CUI [1,1])
C0205272 (UMLS CUI [1,2])
Cardiovascular Disease Previous
Item
previous history of any cardiovascular disease
boolean
C0007222 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
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