NCT05338008已完成不适用
Serum and Wound Vancomycin Levels Following Intrawound Administration in Primary Total Hip Arthroplasty
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 120
- 试验地点
- 1
- 主要终点
- Blood loss
研究概览
简要总结
The purpose of this study is to determine the intra-articular and serum levels of vancomycin over the first 24 hours postoperatively after intra-articular administration of a standard dose of vancomycin in primary total hip arthroplasty.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Outcomes Assessor)
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
- •Age over 18;
- •Total hip arthroplasty for advanced hip diseases including femoral neck fracture, developmental dysplasia of hip, and osteonecrosis of the femoral head.
排除标准
- •Diminished mental capacity
- •Vancomycin allergy
- •Chronic kidney disease stage III and stage IV
结局指标
主要结局
Blood loss
时间窗: Postoperative Day 3
Renal function
时间窗: Postoperative Day 1 and Day 3
blood urea nitrogen (BUN), creatinine (Cr), GFR
Intra-articular vancomycin concentration
时间窗: 2 hours, 8 hours and 24 hours postoperatively
Serum vancomycin concentration
时间窗: 2 hours, 8 hours and 24 hours postoperatively
次要结局
未报告次要终点
研究者
Xiang Shuai, MD
Principal Investigator
The Affiliated Hospital of Qingdao University
研究点 (1)
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