Informationen:
Fehler:
ID
31847
Beschreibung
A Proof of Concept and Dose Ranging Study in Patients With Rheumatoid Arthritis; ODM derived from: https://clinicaltrials.gov/show/NCT00713544
Link
https://clinicaltrials.gov/show/NCT00713544
Stichworte
Versionen (1)
- 02.10.18 02.10.18 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
2. Oktober 2018
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Rheumatoid Arthritis NCT00713544
Eligibility Rheumatoid Arthritis NCT00713544
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Rheumatoid Arthritis NCT00713544
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Rheumatoid Arthritis | Swollen joint count | Tender joint count | Elevated erythrocyte sedimentation rate (ESR) Hematologic Test | Elevated C-reactive protein Hematologic Test
Item
diagnosis of ra with active disease defined as: ≥4 swollen joints and ≥6 tender/painful joints, and either have (blood tests) elevated erythrocyte sedimentation rate (esr) or c-reactive protein (crp).
boolean
C0003873 (UMLS CUI [1])
C0451521 (UMLS CUI [2])
C0451530 (UMLS CUI [3])
C1867037 (UMLS CUI [4,1])
C0018941 (UMLS CUI [4,2])
C0742906 (UMLS CUI [5,1])
C0018941 (UMLS CUI [5,2])
C0451521 (UMLS CUI [2])
C0451530 (UMLS CUI [3])
C1867037 (UMLS CUI [4,1])
C0018941 (UMLS CUI [4,2])
C0742906 (UMLS CUI [5,1])
C0018941 (UMLS CUI [5,2])
Rheumatoid factor positive Hematologic Test | Bone erosion Radiographic | Anti-cyclic citrullinated peptide antibody Hematologic Test
Item
at least one of the following: documented history of positive rheumatoid factor (blood test), current presence of positive rheumatoid factor (blood test), baseline radiographic erosion, presence of serum anti-cyclic citrullinated peptide antibodies (bloo
boolean
C0151379 (UMLS CUI [1,1])
C0018941 (UMLS CUI [1,2])
C0587240 (UMLS CUI [2,1])
C0444708 (UMLS CUI [2,2])
C2210597 (UMLS CUI [3,1])
C0018941 (UMLS CUI [3,2])
C0018941 (UMLS CUI [1,2])
C0587240 (UMLS CUI [2,1])
C0444708 (UMLS CUI [2,2])
C2210597 (UMLS CUI [3,1])
C0018941 (UMLS CUI [3,2])
Methotrexate Oral Tablet | Subcutaneous injection of methotrexate
Item
be receiving either: oral (tablets) or subcutaneous (injection) methotrexate for at least 6 months prior to randomisation.
boolean
C1246896 (UMLS CUI [1])
C2585798 (UMLS CUI [2])
C2585798 (UMLS CUI [2])
Inflammatory disorder In addition to Rheumatoid Arthritis | Interference Clinical Trial | Polymyalgia Rheumatica | Giant Cell Arteritis | Arthritis, Reactive
Item
any other inflammatory disease in addition to ra that may interfere with the study (e.g. polymyalgia rheumatica, giant cell arteritis, reactive arthritis, etc).
boolean
C1290884 (UMLS CUI [1,1])
C0332287 (UMLS CUI [1,2])
C0003873 (UMLS CUI [1,3])
C0521102 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C0032533 (UMLS CUI [3])
C0039483 (UMLS CUI [4])
C0085435 (UMLS CUI [5])
C0332287 (UMLS CUI [1,2])
C0003873 (UMLS CUI [1,3])
C0521102 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C0032533 (UMLS CUI [3])
C0039483 (UMLS CUI [4])
C0085435 (UMLS CUI [5])
Chronic pain | Fibromyalgia | Chronic Fatigue Syndrome
Item
current chronic pain disorders including fibromyalgia and chronic fatigue syndromes.
boolean
C0150055 (UMLS CUI [1])
C0016053 (UMLS CUI [2])
C0015674 (UMLS CUI [3])
C0016053 (UMLS CUI [2])
C0015674 (UMLS CUI [3])