ID
31841
Description
Study to Assess the Safety and Efficacy of Modified-Release Prednisone (Lodotra®) Therapy in Patients With Active Rheumatoid Arthritis; ODM derived from: https://clinicaltrials.gov/show/NCT00650078
Link
https://clinicaltrials.gov/show/NCT00650078
Keywords
Versions (3)
- 10/2/18 10/2/18 -
- 10/2/18 10/2/18 -
- 9/20/21 9/20/21 -
Copyright Holder
See clinicaltrials.gov
Uploaded on
October 2, 2018
DOI
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License
Creative Commons BY-NC 3.0
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Eligibility Rheumatoid Arthritis NCT00650078
Eligibility Rheumatoid Arthritis NCT00650078
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
ID.6
Data type
boolean
Description
Synovectomy
Data type
boolean
Alias
- UMLS CUI [1]
- C0185304
Description
Glucocorticoids
Data type
boolean
Alias
- UMLS CUI [1]
- C0017710
Description
Glucocorticoids, Systemic
Data type
boolean
Alias
- UMLS CUI [1]
- C3540777
Description
Glucocorticoids Intermittent administration
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0017710
- UMLS CUI [1,2]
- C0444735
Description
Joint injection
Data type
boolean
Alias
- UMLS CUI [1]
- C0848063
Description
Topical glucocorticoid To be stopped
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0017712
- UMLS CUI [1,2]
- C1272691
Description
Biological agents | Tumor necrosis factor alpha (TNF-) inhibitors
Data type
boolean
Alias
- UMLS CUI [1]
- C0005515
- UMLS CUI [2]
- C3653350
Description
Pregnancy | Breast Feeding
Data type
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
Similar models
Eligibility Rheumatoid Arthritis NCT00650078
- StudyEvent: Eligibility
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0003873 (UMLS CUI [1,4])
C0449238 (UMLS CUI [1,2])
C0444735 (UMLS CUI [1,2])
C1272691 (UMLS CUI [1,2])
C3653350 (UMLS CUI [2])
C0006147 (UMLS CUI [2])