ACTRN12610000434099已完成4 期
Modified HM3 versus Modulith SLX-F2 lithotripter: A prospective randomized trial to compare the clinical efficacy and complication rate between the first and the latest lithotriptor generation in patients with kidney and/or ureteral stones.
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 800
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
- Open (masking not used)
入排标准
- 年龄范围
- o limit 至 o limit（—）
- 性别
- All
入选标准
- •Every patient requiring extracorporeal shock wave lithotripsy after written informed consent.
排除标准
- •Patients referred for treatment with HM3. After prior unsuccessful extracorporeal shock wave lithotripsy for the same stone in another hospital. Patients with staghorn calculi or stones with a diameter larger than 30mm. In case of technical problems with the randomly assigned lithotripter on the day of intervention or impossibility to localize the calculus with the randomly assigned lithotripter.
- •Thrombocytes <100x10/9 per L, prothrombin time < 60%, pregnancy, urinary tract infection, intake of non-steroidal anti-inflammatory drugs within the last 48 hours or ingestion of platelet inhibiting agents within the last 7-10 days.
研究者
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