ID

19968

Description

SYNCHRO. Evaluation of the Forecasts Parameters of Real Time-three-dimensional Doppler Echocardiography in Selecting Patients With Chronic Heart Failure for Cardiac Resynchronisation Therapy; ODM derived from: https://clinicaltrials.gov/show/NCT00488410

Lien

https://clinicaltrials.gov/show/NCT00488410

Mots-clés

Versions (1)
  1. 01/02/2017 01/02/2017 -
Téléchargé le

1 février 2017

DOI

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Licence

Creative Commons BY 4.0
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Eligibility Chronic Heart Failure NCT00488410

Anglais

Eligibility Chronic Heart Failure NCT00488410

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
both gender
Description

Gender

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
age>18 years
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
patients in functional class nyha iii or iv
Description

New York Heart Association Classification Class Functional

Type de données

boolean

Alias
UMLS CUI [1,1]
C1275491
UMLS CUI [1,2]
C0456387
UMLS CUI [1,3]
C0205245
patient with ejection fraction <or=150msec or with qrs between 120 and 149 msec but with echocardiographic evidences for cardiac dyssynchrony, such as those retained in the care-hf trial, e.g.two from the three following criterions :-aortic pre-ejection delay>140msec
Description

Cardiac ejection fraction

Type de données

boolean

Alias
UMLS CUI [1]
C0232174
interventricular mechanical delay >40msec
Description

DELAY INTRAVENTRICULAR Mechanical

Type de données

boolean

Alias
UMLS CUI [1,1]
C0741914
UMLS CUI [1,2]
C0443254
delayed activation of the left ventricular postero-lateral wall
Description

Left Ventricular Conduction Delay

Type de données

boolean

Alias
UMLS CUI [1]
C2984922
patient under optimal treatment for chronic heart failure for at least one month before inclusion
Description

Therapeutic procedure Optimal Chronic heart failure

Type de données

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C2698651
UMLS CUI [1,3]
C0264716
written informed consentement
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient with atrial fibrillation
Description

Atrial Fibrillation

Type de données

boolean

Alias
UMLS CUI [1]
C0004238
absence of echogenicity
Description

Echogenicity Absent

Type de données

boolean

Alias
UMLS CUI [1,1]
C1719852
UMLS CUI [1,2]
C0332197
patient with an indication for pacemaker implantation
Description

Indication Implantation of cardiac pacemaker

Type de données

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0189842
patient suffering from arterial pressure disorders, with systolic pressure greater than 170 or lower than 80 mmhg
Description

pressure on artery Disease | Abnormal systolic arterial pressure

Type de données

boolean

Alias
UMLS CUI [1,1]
C0456363
UMLS CUI [1,2]
C0012634
UMLS CUI [2]
C0277883
major cardiovascular event within 6 weeks before inclusion
Description

Cardiovascular event Major

Type de données

boolean

Alias
UMLS CUI [1,1]
C1320716
UMLS CUI [1,2]
C0205164
patient in the exclusion period of any other clinical trial
Description

Study Subject Participation Status | Clinical Trial Exclusion Period

Type de données

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C0008976
UMLS CUI [2,2]
C2828389
UMLS CUI [2,3]
C1948053
patient without social insurance policy
Description

social; insurance insufficient

Type de données

boolean

Alias
UMLS CUI [1]
C1408694
drug or alcohol addiction
Description

Substance Dependence

Type de données

boolean

Alias
UMLS CUI [1]
C0038580
any psychological disorder
Description

Mental disorder

Type de données

boolean

Alias
UMLS CUI [1]
C0004936
pregnant women
Description

Pregnancy

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
patient with a transplanted organ
Description

Transplanted organ

Type de données

boolean

Alias
UMLS CUI [1]
C0524930
hiv positive serology at inclusion
Description

HIV Seropositivity

Type de données

boolean

Alias
UMLS CUI [1]
C0019699
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Similar models

Eligibility Chronic Heart Failure NCT00488410

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Gender
Item
both gender
boolean
C0079399 (UMLS CUI [1])
Age
Item
age>18 years
boolean
C0001779 (UMLS CUI [1])
New York Heart Association Classification Class Functional
Item
patients in functional class nyha iii or iv
boolean
C1275491 (UMLS CUI [1,1])
C0456387 (UMLS CUI [1,2])
C0205245 (UMLS CUI [1,3])
Cardiac ejection fraction
Item
patient with ejection fraction <or=150msec or with qrs between 120 and 149 msec but with echocardiographic evidences for cardiac dyssynchrony, such as those retained in the care-hf trial, e.g.two from the three following criterions :-aortic pre-ejection delay>140msec
boolean
C0232174 (UMLS CUI [1])
DELAY INTRAVENTRICULAR Mechanical
Item
interventricular mechanical delay >40msec
boolean
C0741914 (UMLS CUI [1,1])
C0443254 (UMLS CUI [1,2])
Left Ventricular Conduction Delay
Item
delayed activation of the left ventricular postero-lateral wall
boolean
C2984922 (UMLS CUI [1])
Therapeutic procedure Optimal Chronic heart failure
Item
patient under optimal treatment for chronic heart failure for at least one month before inclusion
boolean
C0087111 (UMLS CUI [1,1])
C2698651 (UMLS CUI [1,2])
C0264716 (UMLS CUI [1,3])
Informed Consent
Item
written informed consentement
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Atrial Fibrillation
Item
patient with atrial fibrillation
boolean
C0004238 (UMLS CUI [1])
Echogenicity Absent
Item
absence of echogenicity
boolean
C1719852 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Indication Implantation of cardiac pacemaker
Item
patient with an indication for pacemaker implantation
boolean
C3146298 (UMLS CUI [1,1])
C0189842 (UMLS CUI [1,2])
pressure on artery Disease | Abnormal systolic arterial pressure
Item
patient suffering from arterial pressure disorders, with systolic pressure greater than 170 or lower than 80 mmhg
boolean
C0456363 (UMLS CUI [1,1])
C0012634 (UMLS CUI [1,2])
C0277883 (UMLS CUI [2])
Cardiovascular event Major
Item
major cardiovascular event within 6 weeks before inclusion
boolean
C1320716 (UMLS CUI [1,1])
C0205164 (UMLS CUI [1,2])
Study Subject Participation Status | Clinical Trial Exclusion Period
Item
patient in the exclusion period of any other clinical trial
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2,1])
C2828389 (UMLS CUI [2,2])
C1948053 (UMLS CUI [2,3])
social; insurance insufficient
Item
patient without social insurance policy
boolean
C1408694 (UMLS CUI [1])
Substance Dependence
Item
drug or alcohol addiction
boolean
C0038580 (UMLS CUI [1])
Mental disorder
Item
any psychological disorder
boolean
C0004936 (UMLS CUI [1])
Pregnancy
Item
pregnant women
boolean
C0032961 (UMLS CUI [1])
Transplanted organ
Item
patient with a transplanted organ
boolean
C0524930 (UMLS CUI [1])
HIV Seropositivity
Item
hiv positive serology at inclusion
boolean
C0019699 (UMLS CUI [1])
Retour au début de la page 

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