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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 12 December 2020
Main ID:  NCT03784261
Date of registration: 17/12/2018
Prospective Registration: Yes
Primary sponsor: Shinshu University
Public title: Usefulness of Non TNF Usage in RA Patients
Scientific title: Usefulness of Non TNF Usage in Rheumatoid Arthritis Patients
Date of first enrolment: December 17, 2018
Target sample size: 90
Recruitment status: Recruiting
URL:  https://clinicaltrials.gov/show/NCT03784261
Study type:  Interventional
Study design:  Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Single (Participant).  
Phase:  Phase 2
Countries of recruitment
Japan
Contacts
Name:     Yukio Nakamura, MD, PhD
Address: 
Telephone: +81-263-37-2659
Email: yxn14@aol.jp
Affiliation: 
Key inclusion & exclusion criteria

Inclusion Criteria:

┬ĚRA patients

Exclusion Criteria:

- Not RA patients

- RA patients who are allergic to the drugs, refused to do this research, or who are
pregnant



Age minimum: 20 Years
Age maximum: 100 Years
Gender: All
Health Condition(s) or Problem(s) studied
Rheumatoid Arthritis
Intervention(s)
Drug: Drug: "Abatacept"
Drug: Drug: "Salirumab"
Drug: Drug: "Tocilizmab"
Primary Outcome(s)
Assessment of adverse event in rheumatoid arthritis patients for 1 year treated by salirumab (N=30), tocilizumab (N=30), or abatacept (N=30). [Time Frame: at 1 year]
Change from Baseline Values of DAS28-CRP [Time Frame: Baseline and 1 year]
Secondary Outcome(s)
Secondary ID(s)
NonTNF 2018
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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