Eligibility Rheumatoid Arthritis NCT01071798

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
adult patients, >/= 18 years of age
Beskrivning

ID.1

Datatyp

boolean

severe active rheumatoid arthritis; eligible for treatment with rituximab according to current spc
Beskrivning

ID.2

Datatyp

boolean

informed consent to data collection
Beskrivning

ID.3

Datatyp

boolean

ongoing contraception (for female patients only)
Beskrivning

ID.4

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
previous treatment with rituximab (mabthera)
Beskrivning

ID.5

Datatyp

boolean

allergy against monoclonal antibodies, respectively chimeric monoclonal antibodies
Beskrivning

ID.6

Datatyp

boolean

active severe infection
Beskrivning

ID.7

Datatyp

boolean

severe heart failure (nyha class iv) or severe, uncontrolled cardiac disease
Beskrivning

ID.8

Datatyp

boolean

treatment in other studies within 3 months before rituximab therapy
Beskrivning

ID.9

Datatyp

boolean

pregnancy or breast feeding
Beskrivning

ID.10

Datatyp

boolean

Similar models

Eligibility Rheumatoid Arthritis NCT01071798

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
adult patients, >/= 18 years of age
boolean
ID.2
Item
severe active rheumatoid arthritis; eligible for treatment with rituximab according to current spc
boolean
ID.3
Item
informed consent to data collection
boolean
ID.4
Item
ongoing contraception (for female patients only)
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
previous treatment with rituximab (mabthera)
boolean
ID.6
Item
allergy against monoclonal antibodies, respectively chimeric monoclonal antibodies
boolean
ID.7
Item
active severe infection
boolean
ID.8
Item
severe heart failure (nyha class iv) or severe, uncontrolled cardiac disease
boolean
ID.9
Item
treatment in other studies within 3 months before rituximab therapy
boolean
ID.10
Item
pregnancy or breast feeding
boolean