TCTR20180608001招募中4 期
Comparing efficacy of loading and non-loading colchicine in acute crystal induced arthritis
none0 个研究点目标入组 80 人开始时间: 2018年6月8日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 发起方
- 入组人数
- 80
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 Years 至 99 Years（—）
- 性别
- All
入选标准
- •- Patients aged 18 years or older.
- •- Acute CPPD or gout arthritis within 48 hours, confirmed with synovial fluid examination or diagnosed by ACR/EULAR CLASSIFIACTION CRITERIA FOR GOUT 2015.
- •- Never exposed to uric lowering agent, or use uric lowering agent in stable dose for at lease 30 days.
- •- Prescribed colchicine 0.6 mg. per day or less
- •- Prescribed prednisolon 5 mg. per day or lass
排除标准
- •- Co-exiting other causes of arthritis.
- •- Patients who have contraindication to colchicine.
- •- Patient who received analgesic or NSAIDs before included.
- •- eGFR less than 30 by Cockcroft-Gault equation
- •- Patients who cannot estimate pain score
- •- Patients who have significantly severe co-mordities.
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