ACTRN12609000063213已完成3 期
Randomised controlled trial of intravenous antivenom versus placebo in the treatment of pain and systemic effects in redback spider bite
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 240
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 7 Years 至 o limit（—）
- 性别
- All
入选标准
- •1.A definite or likely redback spider bite according to either of the following criteria:
- •a.The spider causing the bite was clearly identified by the patient or clinician, OR
- •b.A clinical syndrome consistent with typical redback spider envenoming, that is the sensation of a bite followed by two or more of:
- •1. increasing pain over the first hour
- •2. radiating, regional or generalised pain
- •3. local or regional diaphoresis
- •2.The treating clinician would normally treat the patient with antivenom, namely either for:
- •1. moderate envenoming = moderate to severe local pain without systemic envenoming, or;
- •2. severe envenoming = moderate to severe local pain and systemic features
排除标准
- •1.Patients who have received antivenom for this envenoming prior to enrolment
- •2.Children aged <8 years because of unreliability of the Verbal Numerical Rating Scale for assessment of pain in this group
- •3.Presentation to hospital >36 hours after the bite
研究者
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