CTRI/2024/06/068527尚未招募4 期
Graft Rinse prior to reperfusion In LDLT, an RCT : GRIT Trial
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- incidence of postreperfusion syndrome between
研究概览
简要总结
This study is to compare the incidence of postreperfusion syndrome between the control group (graft rinse with retrograde filling) and the intervention group (graft rinse with HETA starch solution) during liver transplantation to reduce the post-perfusion syndrome and improve post-operative outcomes.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- None
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)(—)
- 性别
- All
入选标准
- •All adult patients undergoing live donor liver transplantation.
排除标准
- •Patient refusing to consent Pediatric Transplants Patients refusing to consent trial.
结局指标
主要结局
incidence of postreperfusion syndrome between
时间窗: at 5 minutes post-reperfusion,
control group and intervention group
时间窗: at 5 minutes post-reperfusion,
次要结局
- lengths of intensive(care stay & hospital stay, Early allograft Dysfunction,)
研究者
Sudhindran S
Amrita Institute of Medical Sciences and Research Centre
研究点 (1)
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