ID

21491

Description

Early Assessment of Anthracycline-Induced Cardiotoxicity (CARDIOTOX); ODM derived from: https://clinicaltrials.gov/show/NCT00195897

Lien

https://clinicaltrials.gov/show/NCT00195897

Mots-clés

  1. 24/04/2017 24/04/2017 -
Téléchargé le

24 avril 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Lymphoma NCT00195897

Eligibility Lymphoma NCT00195897

  1. StudyEvent: Eligibility
    1. Eligibility Lymphoma NCT00195897
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically proven lymphoma (hodgkin's or non-hodgkin's)
Description

Hodgkin Disease | Lymphoma, Non-Hodgkin

Type de données

boolean

Alias
UMLS CUI [1]
C0019829
UMLS CUI [2]
C0024305
age > 18 y/o and < 70 y/o
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
who score < or = 2
Description

WHO tumor classification

Type de données

boolean

Alias
UMLS CUI [1]
C1301142
life expectancy > 6 mo
Description

Life Expectancy

Type de données

boolean

Alias
UMLS CUI [1]
C0023671
left ventricular ejection fraction > 50%
Description

Left ventricular ejection fraction

Type de données

boolean

Alias
UMLS CUI [1]
C0428772
informed consent
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
previous chemotherapy using anthracyclines
Description

Chemotherapy | Anthracyclines

Type de données

boolean

Alias
UMLS CUI [1]
C0392920
UMLS CUI [2]
C0282564
history of radiation therapy
Description

Therapeutic radiology procedure

Type de données

boolean

Alias
UMLS CUI [1]
C1522449
history of congestive heart failure
Description

Congestive heart failure

Type de données

boolean

Alias
UMLS CUI [1]
C0018802
history of chronic renal insufficiency
Description

Chronic Kidney Insufficiency

Type de données

boolean

Alias
UMLS CUI [1]
C0403447
contra indication to mr examination
Description

Medical contraindication Magnetic Resonance Imaging

Type de données

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0024485
atrial fibrillation and significant arrhythmia
Description

Atrial Fibrillation | Cardiac Arrhythmia

Type de données

boolean

Alias
UMLS CUI [1]
C0004238
UMLS CUI [2]
C0003811
pregnancy
Description

Pregnancy

Type de données

boolean

Alias
UMLS CUI [1]
C0032961

Similar models

Eligibility Lymphoma NCT00195897

  1. StudyEvent: Eligibility
    1. Eligibility Lymphoma NCT00195897
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Hodgkin Disease | Lymphoma, Non-Hodgkin
Item
histologically proven lymphoma (hodgkin's or non-hodgkin's)
boolean
C0019829 (UMLS CUI [1])
C0024305 (UMLS CUI [2])
Age
Item
age > 18 y/o and < 70 y/o
boolean
C0001779 (UMLS CUI [1])
WHO tumor classification
Item
who score < or = 2
boolean
C1301142 (UMLS CUI [1])
Life Expectancy
Item
life expectancy > 6 mo
boolean
C0023671 (UMLS CUI [1])
Left ventricular ejection fraction
Item
left ventricular ejection fraction > 50%
boolean
C0428772 (UMLS CUI [1])
Informed Consent
Item
informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Chemotherapy | Anthracyclines
Item
previous chemotherapy using anthracyclines
boolean
C0392920 (UMLS CUI [1])
C0282564 (UMLS CUI [2])
Therapeutic radiology procedure
Item
history of radiation therapy
boolean
C1522449 (UMLS CUI [1])
Congestive heart failure
Item
history of congestive heart failure
boolean
C0018802 (UMLS CUI [1])
Chronic Kidney Insufficiency
Item
history of chronic renal insufficiency
boolean
C0403447 (UMLS CUI [1])
Medical contraindication Magnetic Resonance Imaging
Item
contra indication to mr examination
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
Atrial Fibrillation | Cardiac Arrhythmia
Item
atrial fibrillation and significant arrhythmia
boolean
C0004238 (UMLS CUI [1])
C0003811 (UMLS CUI [2])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])

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