ID

44723

Descripción

TACkLE Study - Tackling Adverse Chemotherapy-associated Late Effects; ODM derived from: https://clinicaltrials.gov/show/NCT02276430

Link

https://clinicaltrials.gov/show/NCT02276430

Palabras clave

  1. 28/9/21 28/9/21 -
Titular de derechos de autor

University Medical Center Groningen The Netherlands Cancer Institute

Subido en

28 de septiembre de 2021

DOI

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Licencia

Creative Commons BY-NC 4.0

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Eligibility Testicular Cancer NCT02276430

Eligibility Testicular Cancer NCT02276430

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI [1]
C1512693
alive
Descripción

Alive

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2584946
tc diagnosis between 01-01-1976 to 31-12-2007
Descripción

Testicular cancer diagnosis date

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0153594
UMLS CUI [1,2]
C2316983
tc treatment center: umcg, nki/avl, erasmus mc, umcn, lumc
Descripción

Testicular cancer treatment center

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0153594
UMLS CUI [1,2]
C0087111
UMLS CUI [1,3]
C1301943
younger than 50 years of age at tc diagnosis
Descripción

Age of tc diagnosis

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0349644
UMLS CUI [1,2]
C1828181
written informed consent
Descripción

Informed consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
diagnosed with either myocardial infarction (mi), proven coronary artery disease (cad) (ctcae-4 grade 2 or higher) or congestive heart failure (chf) (ctcae-4 grade 2 or higher).
Descripción

Myocardial infarction | Coronary artery disease, ctcae-4 grade | Congestive heart failure, ctcae-4 grade

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2,1]
C1956346
UMLS CUI [2,2]
C2985911
UMLS CUI [3,1]
C0018802
UMLS CUI [3,2]
C2985911
no medical history of cvd before diagnosis of tc
Descripción

No medical history of cardiovascular diseases before diagnosis of tc

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0007222
UMLS CUI [1,2]
C0262926
UMLS CUI [1,3]
C0153594
UMLS CUI [1,4]
C0332152
UMLS CUI [1,5]
C0332197
in order to be eligible to participate in the cardiometabolic risk inventory study (and to be invited to a study assessment), a subject must meet, next to the criteria mentioned in "1)", the following inclusion criteria:
Descripción

in order to be eligible to participate in the cardiometabolic risk inventory study (and to be invited to a study assessment), a subject must meet, next to the criteria mentioned in "1)", the following inclusion criteria:

Alias
UMLS CUI [1]
C1512693
younger than 40 years of age at tc diagnosis
Descripción

Age at the tc diagnosis

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0153594
UMLS CUI [1,2]
C1828181
younger than 75 years of age at moment of inclusion
Descripción

Age at the moment of inclusion

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0001779
UMLS CUI [1,2]
C1512693
UMLS CUI [1,3]
C0681850
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
mental disorder (no informed consent available)
Descripción

Mental disorder

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004936
presence of active malignant disease
Descripción

Active malignant neoplasm

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0205177

Similar models

Eligibility Testicular Cancer NCT02276430

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Inclusion Criteria
C1512693 (UMLS CUI [1])
Alive
Item
alive
boolean
C2584946 (UMLS CUI [1])
Testicular cancer diagnosis date
Item
tc diagnosis between 01-01-1976 to 31-12-2007
boolean
C0153594 (UMLS CUI [1,1])
C2316983 (UMLS CUI [1,2])
Testicular cancer treatment center
Item
tc treatment center: umcg, nki/avl, erasmus mc, umcn, lumc
boolean
C0153594 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C1301943 (UMLS CUI [1,3])
Age of tc diagnosis
Item
younger than 50 years of age at tc diagnosis
boolean
C0349644 (UMLS CUI [1,1])
C1828181 (UMLS CUI [1,2])
Informed consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Myocardial infarction | Coronary artery disease, ctcae-4 grade | Congestive heart failure, ctcae-4 grade
Item
diagnosed with either myocardial infarction (mi), proven coronary artery disease (cad) (ctcae-4 grade 2 or higher) or congestive heart failure (chf) (ctcae-4 grade 2 or higher).
boolean
C0027051 (UMLS CUI [1])
C1956346 (UMLS CUI [2,1])
C2985911 (UMLS CUI [2,2])
C0018802 (UMLS CUI [3,1])
C2985911 (UMLS CUI [3,2])
No medical history of cardiovascular diseases before diagnosis of tc
Item
no medical history of cvd before diagnosis of tc
boolean
C0007222 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
C0153594 (UMLS CUI [1,3])
C0332152 (UMLS CUI [1,4])
C0332197 (UMLS CUI [1,5])
Item Group
in order to be eligible to participate in the cardiometabolic risk inventory study (and to be invited to a study assessment), a subject must meet, next to the criteria mentioned in "1)", the following inclusion criteria:
C1512693 (UMLS CUI [1])
Age at the tc diagnosis
Item
younger than 40 years of age at tc diagnosis
boolean
C0153594 (UMLS CUI [1,1])
C1828181 (UMLS CUI [1,2])
Age at the moment of inclusion
Item
younger than 75 years of age at moment of inclusion
boolean
C0001779 (UMLS CUI [1,1])
C1512693 (UMLS CUI [1,2])
C0681850 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Mental disorder
Item
mental disorder (no informed consent available)
boolean
C0004936 (UMLS CUI [1])
Active malignant neoplasm
Item
presence of active malignant disease
boolean
C0006826 (UMLS CUI [1,1])
C0205177 (UMLS CUI [1,2])

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