Informationen:
Fehler:
ID
34535
Beschreibung
Observational Study of RoActemra/Actemra (Tocilizumab) in Patients With Rheumatoid Arthritis; ODM derived from: https://clinicaltrials.gov/show/NCT01579006
Link
https://clinicaltrials.gov/show/NCT01579006
Stichworte
Versionen (1)
- 19.01.19 19.01.19 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
19. Januar 2019
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Rheumatoid Arthritis NCT01579006
Eligibility Rheumatoid Arthritis NCT01579006
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Rheumatoid Arthritis NCT01579006
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Adult | Age
Item
adult patients, >/= 18 years of age
boolean
C0001675 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0001779 (UMLS CUI [2])
Rheumatoid arthritis disease activity, moderate | Rheumatoid Arthritis Severe
Item
moderate to severe rheumatoid arthritis
boolean
C2368567 (UMLS CUI [1])
C0003873 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0003873 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
Non-Biologic Disease-Modifying Antirheumatic Drug Poor response to treatment | Intolerance to Non-Biologic Disease-Modifying Antirheumatic Drug | Biological agent Quantity Poor response to treatment | Intolerance to Biological agent Quantity
Item
inadequate response (or intolerant) to non-biological dmards or one biologic agent
boolean
C4054347 (UMLS CUI [1,1])
C1320680 (UMLS CUI [1,2])
C1744706 (UMLS CUI [2,1])
C4054347 (UMLS CUI [2,2])
C0005515 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
C1320680 (UMLS CUI [3,3])
C1744706 (UMLS CUI [4,1])
C0005515 (UMLS CUI [4,2])
C1265611 (UMLS CUI [4,3])
C1320680 (UMLS CUI [1,2])
C1744706 (UMLS CUI [2,1])
C4054347 (UMLS CUI [2,2])
C0005515 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
C1320680 (UMLS CUI [3,3])
C1744706 (UMLS CUI [4,1])
C0005515 (UMLS CUI [4,2])
C1265611 (UMLS CUI [4,3])
RoActemra | Actemra
Item
patients initiating treatment with roactemra/actemra on their physician's decision (in accordance with the local label), including patients who started treatment with roactemra/actemra in the 8 weeks prior to the enrolment visit
boolean
C3272237 (UMLS CUI [1])
C2740854 (UMLS CUI [2])
C2740854 (UMLS CUI [2])
RoActemra Previous | Actemra Previous
Item
roactemra/actemra treatment more than 8 weeks prior to the enrolment visit
boolean
C3272237 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C2740854 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
C0205156 (UMLS CUI [1,2])
C2740854 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
RoActemra Previous Clinical Trial | Actemra Previous Clinical Trial | RoActemra Previous Compassionate Use | Actemra Previous Compassionate Use
Item
previous roactemra/actemra treatment in a clinical trial or for compassionate use
boolean
C3272237 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C2740854 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
C0008976 (UMLS CUI [2,3])
C3272237 (UMLS CUI [3,1])
C0205156 (UMLS CUI [3,2])
C2718016 (UMLS CUI [3,3])
C2740854 (UMLS CUI [4,1])
C0205156 (UMLS CUI [4,2])
C2718016 (UMLS CUI [4,3])
C0205156 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C2740854 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
C0008976 (UMLS CUI [2,3])
C3272237 (UMLS CUI [3,1])
C0205156 (UMLS CUI [3,2])
C2718016 (UMLS CUI [3,3])
C2740854 (UMLS CUI [4,1])
C0205156 (UMLS CUI [4,2])
C2718016 (UMLS CUI [4,3])
Study Subject Participation Status | Investigational New Drugs
Item
enrolled in an ongoing clinical trial and/or treatment with any investigational agent within 4 weeks (or 5 half-lives of the investigational agent, whichever is longer) before starting treatment with roactemra/actemra
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C0013230 (UMLS CUI [2])
Autoimmune Disease | Inflammatory joint disease | Exception Rheumatoid Arthritis
Item
history of autoimmune disease or any joint inflammatory disease other than rheumatoid arthritis
boolean
C0004364 (UMLS CUI [1])
C0683381 (UMLS CUI [2])
C1705847 (UMLS CUI [3,1])
C0003873 (UMLS CUI [3,2])
C0683381 (UMLS CUI [2])
C1705847 (UMLS CUI [3,1])
C0003873 (UMLS CUI [3,2])