跳至主要内容
临床试验/CTIS2023-504610-30-01
CTIS2023-504610-30-01进行中(未招募)1 期

Modified autologous leukocyte cells for the treatment of acute kidney injury after cardiac surgery - M2R.AKI.2021

M2rlab S.L.0 个研究点目标入组 116 人开始时间: 2024年5月29日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
116

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
18 至 65+(—)
性别
All

入选标准

  • Patients of both sexes over 18 years of age being able to understand and sign the informed consent., Patients undergoing elective valvular and/or coronary heart surgery performed with extracorporeal circulation., Have a preoperative AKI risk = 30% according to the Leicester Cardiosurgery Scale., Have AKI (serum creatinine >50% increase from baseline) and a urine NGAL value of >200 microgram/g creatinine in the first 48h after cardiac surgery., In the case of women or men of childbearing age, for safety, those who agree to follow the required contraceptive measures from hospital discharge until the end of their participation in the clinical trial.

排除标准

  • Stage IV or V CKD (glomerular filtration rate [GFR] < 30 ml/min), Known severe ventricular dysfunction (left ventricular ejection fraction [LVEF] <30%), Post-surgical septic infection., Participation in another clinical intervention trial., AKI in the month prior to cardiac surgery., Patients previously undergoing renal therapy., Patients who are scheduled to start renal replacement therapy in the following 72 hours, Interstitial glomerulonephritis or vasculitis., Pregnancy., History of renal transplant., Endocarditis., Patients with mechanical assist devices: extracorporeal membrane oxygenator (ECMO), left ventricular assist device (LVAD), right ventricular assist device (RVAD), intra-aortic balloon pumps (IABP).

研究者

发起方
M2rlab S.L.

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