Informações:
Falhas:
ID
31861
Descrição
A Study for Patients With Active Rheumatoid Arthritis Despite Ongoing Methotrexate Therapy; ODM derived from: https://clinicaltrials.gov/show/NCT00785928
Link
https://clinicaltrials.gov/show/NCT00785928
Palavras-chave
Versões (1)
- 04/10/2018 04/10/2018 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
4 de outubro de 2018
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Rheumatoid Arthritis NCT00785928
Eligibility Rheumatoid Arthritis NCT00785928
- StudyEvent: Eligibility
Similar models
Eligibility Rheumatoid Arthritis NCT00785928
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Informed Consent
Item
have given written informed consent
boolean
C0021430 (UMLS CUI [1])
Gender | Risk Absent Pregnancy
Item
women must not be at risk to become pregnant during study participation
boolean
C0079399 (UMLS CUI [1])
C0035647 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0032961 (UMLS CUI [2,3])
C0035647 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0032961 (UMLS CUI [2,3])
Rheumatoid Arthritis
Item
diagnosis of rheumatoid arthritis
boolean
C0003873 (UMLS CUI [1])
Methotrexate Dose Stable
Item
current, regular use of methotrexate, at a stable dose
boolean
C0025677 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
Inclusion criteria Research Personnel
Item
other criteria to be reviewed by study doctor
boolean
C1512693 (UMLS CUI [1,1])
C0035173 (UMLS CUI [1,2])
C0035173 (UMLS CUI [1,2])
Pharmaceutical Preparations Excluded
Item
use of excluded medications(reviewed by study doctor)
boolean
C0013227 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C0332196 (UMLS CUI [1,2])
TNF-alpha blockers Successful treatment
Item
have not failed biologic tnfa inhibitor therapy
boolean
C2170827 (UMLS CUI [1,1])
C0521982 (UMLS CUI [1,2])
C0521982 (UMLS CUI [1,2])
Communicable Disease Study Subject Participation Status At risk
Item
have had recent or ongoing infection which, in the opinion of the study doctor put patient at an unacceptable risk for participation in the study
boolean
C0009450 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C1444641 (UMLS CUI [1,3])
C2348568 (UMLS CUI [1,2])
C1444641 (UMLS CUI [1,3])
Tuberculosis
Item
evidence of tuberculosis
boolean
C0041296 (UMLS CUI [1])
SYSTEMIC INFLAMMATORY PROCESS | Exception Rheumatoid Arthritis | Juvenile rheumatoid arthritis | Crohn Disease | Ulcerative Colitis | Arthritis, Psoriatic | Spondylarthropathy Seronegative
Item
have systemic inflammatory condition other than ra, such as juvenile ra, crohn's disease, ulcerative colitis, psoriatic arthritis or seronegative spondyloarthropathy
boolean
C0749224 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0003873 (UMLS CUI [2,2])
C3714757 (UMLS CUI [3])
C0010346 (UMLS CUI [4])
C0009324 (UMLS CUI [5])
C0003872 (UMLS CUI [6])
C0949691 (UMLS CUI [7,1])
C0521144 (UMLS CUI [7,2])
C1705847 (UMLS CUI [2,1])
C0003873 (UMLS CUI [2,2])
C3714757 (UMLS CUI [3])
C0010346 (UMLS CUI [4])
C0009324 (UMLS CUI [5])
C0003872 (UMLS CUI [6])
C0949691 (UMLS CUI [7,1])
C0521144 (UMLS CUI [7,2])
Exclusion Criteria Research Personnel
Item
other criteria to be reviewed by study doctor
boolean
C0680251 (UMLS CUI [1,1])
C0035173 (UMLS CUI [1,2])
C0035173 (UMLS CUI [1,2])