ID
42829
Description
ODM derived from http://clinicaltrials.gov/show/NCT00502840
Link
http://clinicaltrials.gov/show/NCT00502840
Keywords
Versions (2)
- 12/10/13 12/10/13 - Martin Dugas
- 9/17/21 9/17/21 -
Uploaded on
September 17, 2021
DOI
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License
Creative Commons BY 4.0
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Eligibility NCT00502840 Rheumatoid Arthritis
Eligibility
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI 2011AA
- CL425201
Description
patients who have withdrawn from treatment in ML19070 pre-week 16
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0422727
- SNOMED CT 2011_0131
- 185924006
- UMLS CUI 2011AA
- C2349954
- UMLS CUI 2011AA
- C0039798
Description
patients with a previous response in DAS28 <0.6 to MabThera after week 16
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0205156
- SNOMED CT 2011_0131
- 9130008
- UMLS CUI 2011AA
- C0521982
- SNOMED CT 2011_0131
- 182985004
- UMLS CUI 2011AA
- C2711347
- SNOMED CT 2011_0131
- 441870009
- UMLS CUI 2011AA
- C0732355
- SNOMED CT 2011_0131
- 386919002
- UMLS CUI 2011AA
- C0231290
- SNOMED CT 2011_0131
- 237679004
Description
concurrent treatment with any DMARD except for methotrexate, any TNF alpha inhibitor, or other biologic or investigational agent.
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0009429
- UMLS CUI 2011AA
- C0242708
- UMLS CUI 2011AA
- C1456820
- SNOMED CT 2011_0131
- 39525005
- LOINC Version 232
- MTHU004497
- UMLS CUI 2011AA
- C1554961
- UMLS CUI 2011AA
- C0025677
- SNOMED CT 2011_0131
- 387381009
- LOINC Version 232
- MTHU005020
- UMLS CUI 2011AA
- C1562242
- SNOMED CT 2011_0131
- 420693002
- UMLS CUI 2011AA
- C0005522
- SNOMED CT 2011_0131
- 418980009
- UMLS CUI 2011AA
- C0013230
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