Information:
Fel:
ID
22934
Beskrivning
Evaluation of 2 Oral Doses of PG-760564 in Rheumatoid Arthritis (RA) Patients Receiving Methotrexate; ODM derived from: https://clinicaltrials.gov/show/NCT00369928
Länk
https://clinicaltrials.gov/show/NCT00369928
Nyckelord
Versioner (1)
- 2017-06-17 2017-06-17 -
Uppladdad den
17 juni 2017
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Rheumatoid Arthritis NCT00369928
Eligibility Rheumatoid Arthritis NCT00369928
- StudyEvent: Eligibility
Similar models
Eligibility Rheumatoid Arthritis NCT00369928
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Rheumatoid Arthritis
Item
meet american college of rheumatology (acr) criteria for rheumatoid arthritis
boolean
C0003873 (UMLS CUI [1])
disease length
Item
disease duration of at least 6 months
boolean
C0872146 (UMLS CUI [1])
Methotrexate
Item
must be treated with methotrexate for at least 24 weeks
boolean
C0025677 (UMLS CUI [1])
Swollen joint count | Tender joint count
Item
at least 6 swollen joints and 6 tender joints
boolean
C0451521 (UMLS CUI [1])
C0451530 (UMLS CUI [2])
C0451530 (UMLS CUI [2])
Antirheumatic Drugs, Disease-Modifying | Washout Patient need for
Item
washout required for other disease modifying anti-rheumatic drugs (dmards)
boolean
C0242708 (UMLS CUI [1])
C1710661 (UMLS CUI [2,1])
C0686904 (UMLS CUI [2,2])
C1710661 (UMLS CUI [2,1])
C0686904 (UMLS CUI [2,2])
Childbearing Potential Contraceptive methods | Gender Contraceptive methods
Item
women of childbearing age and all males must use acceptable method of birth control
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0079399 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
C0700589 (UMLS CUI [1,2])
C0079399 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
Tuberculosis
Item
tuberculosis
boolean
C0041296 (UMLS CUI [1])
Malignant Neoplasms
Item
malignancies
boolean
C0006826 (UMLS CUI [1])
Electrocardiogram abnormal
Item
abnormal electrocardiograms as described in the protocol
boolean
C0522055 (UMLS CUI [1])
Communicable Disease | Recurrent infections | Immunologic Deficiency Syndromes
Item
current infection or recurrent infections or immunodeficiency
boolean
C0009450 (UMLS CUI [1])
C0239998 (UMLS CUI [2])
C0021051 (UMLS CUI [3])
C0239998 (UMLS CUI [2])
C0021051 (UMLS CUI [3])
Liver diseases | Liver function tests abnormal
Item
liver diseases and abnormalities in liver function tests as described in the protocol
boolean
C0023895 (UMLS CUI [1])
C0151766 (UMLS CUI [2])
C0151766 (UMLS CUI [2])
Autoimmune Diseases | Rheumatoid Arthritis | Sjogren's Syndrome Secondary to Rheumatoid Arthritis
Item
autoimmune diseases other than ra except sjogren's syndrome secondary to ra;
boolean
C0004364 (UMLS CUI [1])
C0003873 (UMLS CUI [2])
C1527336 (UMLS CUI [3,1])
C0175668 (UMLS CUI [3,2])
C0003873 (UMLS CUI [3,3])
C0003873 (UMLS CUI [2])
C1527336 (UMLS CUI [3,1])
C0175668 (UMLS CUI [3,2])
C0003873 (UMLS CUI [3,3])
Demyelinating Diseases
Item
history of demyelization diseases
boolean
C0011303 (UMLS CUI [1])
Condition Study Subject Participation Status Unfavorable | Laboratory Results Changed status Important | Disease Changed status Important
Item
any condition that in the opinion of the investigator could be detrimental to patients enrolling in the study including clinically important changes in laboratory values and other diseases described in the protocol
boolean
C0348080 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C3640815 (UMLS CUI [1,3])
C1254595 (UMLS CUI [2,1])
C0443172 (UMLS CUI [2,2])
C3898777 (UMLS CUI [2,3])
C0012634 (UMLS CUI [3,1])
C0443172 (UMLS CUI [3,2])
C3898777 (UMLS CUI [3,3])
C2348568 (UMLS CUI [1,2])
C3640815 (UMLS CUI [1,3])
C1254595 (UMLS CUI [2,1])
C0443172 (UMLS CUI [2,2])
C3898777 (UMLS CUI [2,3])
C0012634 (UMLS CUI [3,1])
C0443172 (UMLS CUI [3,2])
C3898777 (UMLS CUI [3,3])