Information:
Fel:
ID
34510
Beskrivning
A Study to Assess the Effect of Tocilizumab Plus Methotrexate on Safety and Signs and Symptoms in Patients With Moderate to Severe Active Rheumatoid Arthritis; ODM derived from: https://clinicaltrials.gov/show/NCT00754572
Länk
https://clinicaltrials.gov/show/NCT00754572
Nyckelord
Versioner (1)
- 2019-01-18 2019-01-18 -
Rättsinnehavare
See clinicaltrials.gov
Uppladdad den
18 januari 2019
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Rheumatoid Arthritis NCT00754572
Eligibility Rheumatoid Arthritis NCT00754572
- StudyEvent: Eligibility
Similar models
Eligibility Rheumatoid Arthritis NCT00754572
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Age | Moderate rheumatoid arthritis Disease length | Rheumatoid Arthritis Severe Disease length
Item
patients >=18 years with moderate to severe active ra for at least 6 months;
boolean
C0001779 (UMLS CUI [1])
C2368567 (UMLS CUI [2,1])
C0872146 (UMLS CUI [2,2])
C0003873 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0872146 (UMLS CUI [3,3])
C2368567 (UMLS CUI [2,1])
C0872146 (UMLS CUI [2,2])
C0003873 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0872146 (UMLS CUI [3,3])
Swollen joint count | Tender joint count
Item
swollen joint count >=6 (66 joint count) and tender joint count >=8 (68 joint count) at screening;
boolean
C0451521 (UMLS CUI [1])
C0451530 (UMLS CUI [2])
C0451530 (UMLS CUI [2])
Methotrexate Dose Stable | Poor response to treatment
Item
inadequate response to stable dose of mtx;
boolean
C0025677 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C1320680 (UMLS CUI [2])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C1320680 (UMLS CUI [2])
Females & males of reproductive potential Contraceptive methods
Item
patients of reproductive potential must be using a reliable means of contraception.
boolean
C4034483 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0700589 (UMLS CUI [1,2])
Autoimmune Disease Rheumatic | Exception Rheumatoid Arthritis
Item
rheumatic autoimmune disease other than ra;
boolean
C0004364 (UMLS CUI [1,1])
C0035435 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0003873 (UMLS CUI [2,2])
C0035435 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0003873 (UMLS CUI [2,2])
Rheumatoid Arthritis Functional Status Class
Item
patients with functional class iv ra;
boolean
C0003873 (UMLS CUI [1,1])
C0598463 (UMLS CUI [1,2])
C0456387 (UMLS CUI [1,3])
C0598463 (UMLS CUI [1,2])
C0456387 (UMLS CUI [1,3])
Juvenile rheumatoid arthritis | Rheumatoid Arthritis Relationship Age | Inflammatory joint disease Except Rheumatoid Arthritis
Item
diagnosis of juvenile idiopathic or rheumatoid arthritis before age 16 or a history of current inflammatory joint disease other than ra;
boolean
C3714757 (UMLS CUI [1])
C0003873 (UMLS CUI [2,1])
C0439849 (UMLS CUI [2,2])
C0001779 (UMLS CUI [2,3])
C0683381 (UMLS CUI [3,1])
C0332300 (UMLS CUI [3,2])
C0003873 (UMLS CUI [3,3])
C0003873 (UMLS CUI [2,1])
C0439849 (UMLS CUI [2,2])
C0001779 (UMLS CUI [2,3])
C0683381 (UMLS CUI [3,1])
C0332300 (UMLS CUI [3,2])
C0003873 (UMLS CUI [3,3])
Anti-tumor necrosis factor therapy failed
Item
prior treatment failure with anti-tumor necrosis factor agent;
boolean
C0281481 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
pregnant or breastfeeding women.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])