NCT07659886尚未招募3 期
Implementation of Vancomycin Powder Application in the Emergency Department for Open Fractures
干预措施
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 入组人数
- 100
- 试验地点
- 1
研究概览
简要总结
To evaluate the feasibility, safety, and potential efficacy of applying vancomycin powder locally to open fractures in the emergency department prior to definitive surgical intervention.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Participants aged 18 years or older presenting to the Emergency Department with Gustilo-Anderson Type I, II, or III open fractures.
排除标准
- •Known allergy to vancomycin
- •Ballistic open fractures
- •Pregnancy
- •Currently breastfeeding
- •Age younger than 18 years.
研究组 & 干预措施
Emergency Department Vancomycin Powder
Experimental
Patients receive 1 gram topical vancomycin powder applied to the open fracture wound in the Emergency Department in addition to standard open fracture management.
干预措施: Vancomycin (VAN) treatment (Drug)
Standard Open Fracture Care
Active Comparator
Patients receive standard open fracture management without Emergency Department (ED) vancomycin powder.
干预措施: Standard Open Fracture Care (Other)
研究者
Kristen De Wilde
Resident physician
Atlantic Health System
研究点 (1)
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