DRKS00018931已完成3 期
Remote Ischemic Preconditioning (RIPC) versus sham-control for reduction of ischemia-reperfusion injury of the Liver after liver surgery in patients with pre-damaged liver: a prospective, randomized controlled, triple-blind, clinical phase III monocenter trial - RIP
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 102
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
- Randomized controlled study
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 one（—）
- 性别
- All
入选标准
- •Persons meeting the following criteria may be included in the study:
- •Known pre-damage to the liver (e.g. liver cirrhosis (Child Pugh A and B), steatosis, fibrosis, s/p chemotherapy, other pathologies leading to liver damage)
- •Planned elective liver resection or dissection of the liver tissue (so-called in situ split) with subsequent resection
- •Signed informed consent
- •Age =18 years
排除标准
- •Persons meeting any of the following criteria cannot be included in the study:
- •Patients not able to give informed consent
- •Liver cirrhosis Child Pugh C
- •Patients presenting with the following contraindications to the study intervention (RIPC): arterial occlusive disease (AOD), infections or wounds on the upper extremity, poorly controlled diabetes mellitus, or deep vein thrombosis of the upper extremity
- •Patients in whom a Pringle maneuver is unlikely due to the type of procedure or extent of resection (e.g. very small and/or peripheral resections)
研究者
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