TCTR20230222010已完成3 期
A Prospective Randomized Controlled Trial comparing the Efficacy of Dexamethasone versus Triamcinolone Acetonide Injection for the Treatment of Primary Trigger
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 123
研究概览
简要总结
Resolution of symptoms at 4 weeks of Dexamethasone group was 90.6 percent and Triamcinolone group 89.1 percent. no statistical significant, p-value 0.07
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 Years 至 N/A (No limit)（—）
- 性别
- All
入选标准
- •Primary Trigger Finger Grade I II IIIA IIIB
- •No prior treatment
排除标准
- •Inflammatory joint disease
- •Prior trauma
- •Uncontrolled DM
- •Allergic to steroid or local anesthetic drug
研究者
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