ID
31841
Beschrijving
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
Trefwoorden
Versies (3)
- 02-10-18 02-10-18 -
- 02-10-18 02-10-18 -
- 20-09-21 20-09-21 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
2 oktober 2018
DOI
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Licentie
Creative Commons BY-NC 3.0
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Eligibility Rheumatoid Arthritis NCT00650078
Eligibility Rheumatoid Arthritis NCT00650078
- StudyEvent: Eligibility
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschrijving
ID.6
Datatype
boolean
Beschrijving
Synovectomy
Datatype
boolean
Alias
- UMLS CUI [1]
- C0185304
Beschrijving
Glucocorticoids
Datatype
boolean
Alias
- UMLS CUI [1]
- C0017710
Beschrijving
Glucocorticoids, Systemic
Datatype
boolean
Alias
- UMLS CUI [1]
- C3540777
Beschrijving
Glucocorticoids Intermittent administration
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0017710
- UMLS CUI [1,2]
- C0444735
Beschrijving
Joint injection
Datatype
boolean
Alias
- UMLS CUI [1]
- C0848063
Beschrijving
Topical glucocorticoid To be stopped
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0017712
- UMLS CUI [1,2]
- C1272691
Beschrijving
Biological agents | Tumor necrosis factor alpha (TNF-) inhibitors
Datatype
boolean
Alias
- UMLS CUI [1]
- C0005515
- UMLS CUI [2]
- C3653350
Beschrijving
Pregnancy | Breast Feeding
Datatype
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])