Eligibility NCT00502840 Rheumatoid Arthritis

ODM derived from http://clinicaltrials.gov/show/NCT00502840

Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Inclusion Criteria
CL425202 (UMLS CUI 2011AA)
age 18 Years to 75 Years
Item
age 18 Years to 75 Years
boolean
C0001779 (UMLS CUI 2011AA)
397669002 (SNOMED CT 2011_0131)
adult patients with rheumatoid arthritis who participated in ML19070, and have completed the week 24 visit
Item
adult patients with rheumatoid arthritis who participated in ML19070, and have completed the week 24 visit
boolean
C0700597 (UMLS CUI 2011AA)
41847000 (SNOMED CT 2011_0131)
C0003873 (UMLS CUI 2011AA)
69896004 (SNOMED CT 2011_0131)
10039073 (MedDRA 14.1)
M06.9 (ICD-10-CM Version 2010)
714.0 (ICD-9-CM Version 2011)
C0011900 (UMLS CUI 2011AA)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
C0681850 (UMLS CUI 2011AA)
C0205197 (UMLS CUI 2011AA)
255594003 (SNOMED CT 2011_0131)
C0585339 (UMLS CUI 2011AA)
396149002 (SNOMED CT 2011_0131)
C1512346 (UMLS CUI 2011AA)
ENC (HL7 V3 2006_05)
eligible for re-treatment (DAS28 >2.6 after week 24, swollen joint count >=4, tender joint count >=4).
Item
eligible for re-treatment (DAS28 >2.6 after week 24, swollen joint count >=4, tender joint count >=4).
boolean
C1302261 (UMLS CUI 2011AA)
399223003 (SNOMED CT 2011_0131)
C0376495 (UMLS CUI 2011AA)
C2711347 (UMLS CUI 2011AA)
441870009 (SNOMED CT 2011_0131)
C0231290 (UMLS CUI 2011AA)
237679004 (SNOMED CT 2011_0131)
C2825407 (UMLS CUI 2011AA)
C0439234 (UMLS CUI 2011AA)
258707000 (SNOMED CT 2011_0131)
Y (HL7 V3 2006_05)
C0451521 (UMLS CUI 2011AA)
273856009 (SNOMED CT 2011_0131)
C0451530 (UMLS CUI 2011AA)
273865002 (SNOMED CT 2011_0131)
Item Group
Exclusion Criteria
CL425201 (UMLS CUI 2011AA)
patients who have withdrawn from treatment in ML19070 pre-week 16
Item
patients who have withdrawn from treatment in ML19070 pre-week 16
boolean
C0422727 (UMLS CUI 2011AA)
185924006 (SNOMED CT 2011_0131)
C2349954 (UMLS CUI 2011AA)
C0039798 (UMLS CUI 2011AA)
patients with a previous response in DAS28 <0.6 to MabThera after week 16
Item
patients with a previous response in DAS28 <0.6 to MabThera after week 16
boolean
C0205156 (UMLS CUI 2011AA)
9130008 (SNOMED CT 2011_0131)
C0521982 (UMLS CUI 2011AA)
182985004 (SNOMED CT 2011_0131)
C2711347 (UMLS CUI 2011AA)
441870009 (SNOMED CT 2011_0131)
C0732355 (UMLS CUI 2011AA)
386919002 (SNOMED CT 2011_0131)
C0231290 (UMLS CUI 2011AA)
237679004 (SNOMED CT 2011_0131)
concurrent treatment with any DMARD except for methotrexate, any TNF alpha inhibitor, or other biologic or investigational agent.
Item
concurrent treatment with any DMARD except for methotrexate, any TNF alpha inhibitor, or other biologic or investigational agent.
boolean
C0009429 (UMLS CUI 2011AA)
C0242708 (UMLS CUI 2011AA)
C1456820 (UMLS CUI 2011AA)
39525005 (SNOMED CT 2011_0131)
MTHU004497 (LOINC Version 232)
C1554961 (UMLS CUI 2011AA)
C0025677 (UMLS CUI 2011AA)
387381009 (SNOMED CT 2011_0131)
MTHU005020 (LOINC Version 232)
C1562242 (UMLS CUI 2011AA)
420693002 (SNOMED CT 2011_0131)
C0005522 (UMLS CUI 2011AA)
418980009 (SNOMED CT 2011_0131)
C0013230 (UMLS CUI 2011AA)

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