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Low Dose Rituximab as a First Line Biologic Therapy for the Treatment of DMARD Resistant Patients With Rheumatoid Arthritis

Phase 4
Completed
Conditions
DMARD Resistant Rheumatoid Arthritis
Interventions
Registration Number
NCT01593332
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

In this project the investigators decide to evaluate the efficacy and safety of half dose mabthera (it means 500 mg infusion two weeks apart) in conventional drug resistant cases of rheumatoid arthritis. The investigators choose this drug because the use of anti-TNF drugs limited in the investigators refractory patients as the first line drugs because of its cost.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
44
Inclusion Criteria
  • 1987 ACR criteria for classification of RA
  • Positive for rheumatoid factor(RF)
  • Active RA despite therapy with conventional for at least 3 months as evidenced by DAS 28 > 3/2
  • Patients with active, resistant RA who didn't receive anti TNF agents.
Exclusion Criteria
  • Patient with hypogammaglobulinemia
  • Patient with congestive heart failure (classIV)
  • Active current bacterial,viral,fungal,myocardial or other infections
  • Chronic hepatitis B or hepatitis C carriers
  • History of severe allergic reaction to human,humanized or murine monoclonal antibodies
  • History of malignancies
  • Pregnant women or lactating mothers 8) Patients with Chronic renal failure and hepatic disease.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
MethotrexateRituximab-
RituximabRituximab-
Primary Outcome Measures
NameTimeMethod
change in 28-joint disease activity index( DAS28)Study duration was 6 months and the subjects were assessed for DAS 28 change at baseline, after 2 , 16 and 24 weeks.

disease activity score 28 formula which caculates based the number of tenderness and swelling of 28 joints and also ESR)

Change in European league against rheumatism(EULAR) response criteriaChange in EULAR 2,16,24 weeks
Secondary Outcome Measures
NameTimeMethod
Rituximab side effects0,2,16,24 weeks

side effects like infusion reaction , paresthesia, itching,hypertension or hypotension,headache and infection.

Trial Locations

Locations (1)

Rheumatic Diseases Research Center, Mashhad University of Medical Sciences

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Mashhad, Khorasan Razavi, Iran, Islamic Republic of

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