Information:
Fel:
ID
31877
Beskrivning
Long-term Treatment Study of Certolizumab Pegol Without Coadministration of Methotrexate in Japanese Rheumatoid Arthritis (RA) Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00850343
Länk
https://clinicaltrials.gov/show/NCT00850343
Nyckelord
Versioner (1)
- 2018-10-06 2018-10-06 -
Rättsinnehavare
See clinicaltrials.gov
Uppladdad den
6 oktober 2018
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Rheumatoid Arthritis NCT00850343
Eligibility Rheumatoid Arthritis NCT00850343
- StudyEvent: Eligibility
Similar models
Eligibility Rheumatoid Arthritis NCT00850343
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Study Subject Participation Status | Clinical Trial Specified | Criteria Fulfill
Item
subjects who participated in study 275-08-003 and meet all of the criteria described below.
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2,1])
C0205369 (UMLS CUI [2,2])
C0243161 (UMLS CUI [3,1])
C1550543 (UMLS CUI [3,2])
C0008976 (UMLS CUI [2,1])
C0205369 (UMLS CUI [2,2])
C0243161 (UMLS CUI [3,1])
C1550543 (UMLS CUI [3,2])
ACR Criteria failed | Clinical Trial Specified Premature Discontinued | Clinical Trial Specified Completed
Item
patients who did not reach acr20, and prematurely discontinued study 275-08-003 at week 16 or completed study 275-08-003 by week 24.
boolean
C3273747 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
C0008976 (UMLS CUI [2,1])
C0205369 (UMLS CUI [2,2])
C4018905 (UMLS CUI [2,3])
C1444662 (UMLS CUI [2,4])
C0008976 (UMLS CUI [3,1])
C0205369 (UMLS CUI [3,2])
C0205197 (UMLS CUI [3,3])
C0231175 (UMLS CUI [1,2])
C0008976 (UMLS CUI [2,1])
C0205369 (UMLS CUI [2,2])
C4018905 (UMLS CUI [2,3])
C1444662 (UMLS CUI [2,4])
C0008976 (UMLS CUI [3,1])
C0205369 (UMLS CUI [3,2])
C0205197 (UMLS CUI [3,3])
Protocol Deviation Important
Item
patients who experienced an important protocol deviation as mentioned below during study 275-08-003.
boolean
C1705236 (UMLS CUI [1,1])
C3898777 (UMLS CUI [1,2])
C3898777 (UMLS CUI [1,2])
Live Vaccine | Exception Influenza | Exception Pneumococcal vaccine
Item
patients who received live or attenuated vaccines during study 275-08-003 (except for influenza or pneumococcal vaccines).
boolean
C0042211 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0021400 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0358314 (UMLS CUI [3,2])
C1705847 (UMLS CUI [2,1])
C0021400 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0358314 (UMLS CUI [3,2])
Tuberculosis Chest X-ray
Item
patients who were found to have tuberculosis on a chest x-ray during study 275-08-003.
boolean
C0041296 (UMLS CUI [1,1])
C0039985 (UMLS CUI [1,2])
C0039985 (UMLS CUI [1,2])
Communicable Disease Same | Treatment required for Quantity
Item
patients who required treatment for the same infection at two or more different times during study 275-08-003
boolean
C0009450 (UMLS CUI [1,1])
C0445247 (UMLS CUI [1,2])
C0332121 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0445247 (UMLS CUI [1,2])
C0332121 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
Pregnancy | Breast Feeding | Childbearing Potential Planned Pregnancy
Item
women who are pregnant, are lactating, of childbearing potential and wish to conceive during the study and post-study 3 months.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C3831118 (UMLS CUI [3,1])
C0032992 (UMLS CUI [3,2])
C0006147 (UMLS CUI [2])
C3831118 (UMLS CUI [3,1])
C0032992 (UMLS CUI [3,2])
Study Subject Participation Status Inappropriate
Item
patients whom the investigator has decided to be inappropriate for participation in the study
boolean
C2348568 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
C1548788 (UMLS CUI [1,2])