ISRCTN15982148进行中（未招募）3 期
The effect of ulinastatin on sepsis-related organ failure in children: a multicenter randomized controlled trial
Guangdong Techpool Bio-pharma Co., Ltd.0 个研究点目标入组 364 人开始时间: 2024年8月29日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 364
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
- 性别
- All
入选标准
- •1. 28 days < age = 18 years
- •2. There is clear evidence of infection
- •3. Meet diagnostic criteria for sepsis: infection + pSOFA and/or Phoenix Sepsis Score (PSS) =2
排除标准
- •1. Received immunomodulatory therapy within 2 months before enrollment, such as Xuebijing and thymosin
- •2. Use of high-dose non-steroidal anti-inflammatory drugs within two days before enrollment; The daily dose of glucocorticoids > 5 mg/kg or greater than 500 mg/day within two days before enrollment
- •3. Palliative treatment without enough life support treatment
- •4. Receive ulinastatin treatment prior to enrollment
- •5. Previous history of allergy to ulinastatin or any of its components
- •6. Children with terminal disease
研究者
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