Informationen:
Fehler:
ID
44723
Beschreibung
TACkLE Study - Tackling Adverse Chemotherapy-associated Late Effects; ODM derived from: https://clinicaltrials.gov/show/NCT02276430
Link
https://clinicaltrials.gov/show/NCT02276430
Stichworte
Versionen (1)
- 28.09.21 28.09.21 -
Rechteinhaber
University Medical Center Groningen The Netherlands Cancer Institute
Hochgeladen am
28. September 2021
DOI
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Lizenz
Creative Commons BY-NC 4.0
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Eligibility Testicular Cancer NCT02276430
Eligibility Testicular Cancer NCT02276430
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Testicular Cancer NCT02276430
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
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])
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])
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])
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])
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])
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])
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])
C1512693 (UMLS CUI [1,2])
C0681850 (UMLS CUI [1,3])
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])
C0205177 (UMLS CUI [1,2])