JPRN-jRCT2031230020招募中3 期
RAvulizumab to PRotect PaTients with Chronic Kidney DisEase (CKD) froM Cardiac Surgery Associated Acute Kidney Injury (CSA-AKI) and Subsequent Major Adverse Kidney Events (MAKE): A Phase 3, Randomized, Double-blind, Placebo-controlled, Multicenter Study - ARTEMIS
Yokosawa Jun0 个研究点目标入组 36 人开始时间: 2023年4月16日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 发起方
- 入组人数
- 36
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- >= 18age old 至 <= 90age old(—)
- 性别
- All
入选标准
- •1. Participant weighs 30 kg more
- •2. Planned non emergent sternotomy with CPB procedure for the following surgeries,
- •Multi vessel CABG
- •Valve replacement or repair, ascending aorta surgery permitted if combined with aortic valve replacement or repair
- •Combined CABG and valve surgery, inclusion of single-vessel CABG when combined with valve replacement or repair is permitted
- •3. Known CKD (Stage 3A, 3B, or 4) for at least 3 months
排除标准
- •1. Emergency or salvage cardiac surgery is expected at screening or randomization, as assessed by the Investigator.
- •2. Single-vessel CABG without valve surgery is planned.
- •3. Off-pump surgery is planned (eg, surgery without CPB).
- •4. Recipient of a solid organ or bone marrow transplantation.
- •5. Cardiogenic shock, hemodynamic instability, use of intra-aortic balloon pump, extracorporeal membrane oxygenation, or left ventricular assist device within 72 hours of randomization.
- •6. Active systemic bacterial, viral, or fungal infection within 14 days prior to randomization.
- •7. History of unexplained, recurrent infection.
- •8. Any use of KRT or presence of AKI within 30 days of randomization
- •9. Use of any complement inhibitors, or plasmapheresis or plasma exchange within the year prior to Screening, or planned use during the course of the study.
- •10. Participant is not willing to be vaccinated against N meningitidis or is unwilling to receive prophylactic treatment with appropriate antibiotics, if needed
- •11. History of or unresolved N meningitidis infection.
研究者
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