End of Treatment GOAL Trial B-cell Lymphoma NCT02499003

End of Treatment
Descrizione

End of Treatment

Alias
UMLS CUI-1
C0580352
Subject-ID
Descrizione

Subject ID

Tipo di dati

text

Alias
UMLS CUI [1]
C2348585
Did the subject complete the treatment cycles?
Descrizione

completion treatment cycles

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0580352
If 'no', please specify reason(s) for early treatment termination: Progression of underlying disease
Descrizione

reason disease progression

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0242656
If 'no', please specify reason(s) for early treatment termination: Adverse event
Descrizione

reason Adverse event

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0877248
If 'Adverse Event', please specify:
Descrizione

specification

Tipo di dati

text

Alias
UMLS CUI [1]
C2348235
If 'no', please specify reason(s) for early treatment termination: Death
Descrizione

reason Death

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0011065
If 'no', please specify reason(s) for early treatment termination: Withdrawal of consent
Descrizione

reason Withdrawal of consent

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C1707492
If 'no', please specify reason(s) for early treatment termination: Non-compliance with protocol
Descrizione

reason non-compliance with protocol

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0525058
UMLS CUI [1,3]
C0558080
UMLS CUI [1,4]
C1299582
If 'Non-compliance with protocol', please specify:
Descrizione

specification

Tipo di dati

text

Alias
UMLS CUI [1]
C2348235
If 'no', please specify reason(s) for early treatment termination: Other
Descrizione

treatment termination

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0871548
If 'Other', please specify:
Descrizione

specify

Tipo di dati

text

Alias
UMLS CUI [1]
C1521902

Similar models

End of Treatment GOAL Trial B-cell Lymphoma NCT02499003

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
End of Treatment
C0580352 (UMLS CUI-1)
Subject ID
Item
Subject-ID
text
C2348585 (UMLS CUI [1])
completion treatment cycles
Item
Did the subject complete the treatment cycles?
boolean
C0580352 (UMLS CUI [1])
reason disease progression
Item
If 'no', please specify reason(s) for early treatment termination: Progression of underlying disease
boolean
C0392360 (UMLS CUI [1,1])
C0242656 (UMLS CUI [1,2])
reason Adverse event
Item
If 'no', please specify reason(s) for early treatment termination: Adverse event
boolean
C0392360 (UMLS CUI [1,1])
C0877248 (UMLS CUI [1,2])
specification
Item
If 'Adverse Event', please specify:
text
C2348235 (UMLS CUI [1])
reason Death
Item
If 'no', please specify reason(s) for early treatment termination: Death
boolean
C0392360 (UMLS CUI [1,1])
C0011065 (UMLS CUI [1,2])
reason Withdrawal of consent
Item
If 'no', please specify reason(s) for early treatment termination: Withdrawal of consent
boolean
C0392360 (UMLS CUI [1,1])
C1707492 (UMLS CUI [1,2])
reason non-compliance with protocol
Item
If 'no', please specify reason(s) for early treatment termination: Non-compliance with protocol
boolean
C0392360 (UMLS CUI [1,1])
C0525058 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,3])
C1299582 (UMLS CUI [1,4])
specification
Item
If 'Non-compliance with protocol', please specify:
text
C2348235 (UMLS CUI [1])
treatment termination
Item
If 'no', please specify reason(s) for early treatment termination: Other
boolean
C0871548 (UMLS CUI [1])
specify
Item
If 'Other', please specify:
text
C1521902 (UMLS CUI [1])