drugset / Trial / NCT03215407

The Comparative Study of Intra-articular Injection of Tocilizumab and Compound Betamethasone

NCT03215407

Phase 4 Unknown 60 enrolled Chinese PLA General Hospital
RandomizedParallel-groupDouble-blindTreatment

Summary

Aim: Comparing the efficacy and safety of intra-articular injection of tocilizumab and compound betamethasone. Study design: A randomized, single-blind, parallel controlled and one center trial design. Sample size: 60 cases. Study content: Patients who meet inclusive criteria will be randomly divided into tocilizumab group and compound betamethasone group. In the baseline period, the investigators will collect patients' general information, disease information, disease activity score, laboratory results and images of articular ultrasound. After 4 weeks of injection, patients will be asked to come back, and their disease information, disease activity score, laboratory results as well as images of articular ultrasound will be collected. Finally, these data will be sorted and analyzed. Hypothesis: The efficacy and safety of intra-articular injection of tocilizumab is better than that of compound betamethasone.

Timeline

Start
2017-08-01
Primary completion
2017-12-12
Completion
2018-03-03

Drugs

EvaluationDrugModalityDoseRoute
Comparator BETAMETHASONE DIPROPIONATE Small molecule 14 mg Other
Subject Tocilizumab Monoclonal antibody 80 mg Other

Indications