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临床试验/NCT03772990
NCT03772990已完成4 期

Calcium Administration in Patients Undergoing Cardiac Surgery Under Cardiopulmonary Bypass (ICARUS Trial): Prospective Randomized, Double-blind Placebo-controlled Superiority Trial

Meshalkin Research Institute of Pathology of Circulation11 个研究点 分布在 3 个国家目标入组 820 人开始时间: 2019年1月14日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
820
试验地点
11
主要终点
Inotropic support

研究概览

简要总结

Termination of cardiopulmonary bypass is a critical step in any cardiac surgical procedure and requires a thorough planning. Debate about rationale of calcium administration during weaning of cardiopulmonary bypass has been conducted for several decades; however, a consensus has not been yet reached.

Perioperative hypocalcemia can develop because of haemodilution or calcium binding from heparin, albumin and citrate. Perioperative hypocalcemia is often complicated by development of arrhythmias, especially QT interval prolongation. Furthermore, low content of calcium can lead to vascular tone disorders, violation of neuromuscular transmission, altered hemostasis and heart failure, resistant to inotropic agents, especially in patients with concomitant cardiomyopathy.

On the other hand, hypercalcaemia is a dangerous complication in cardiac surgery. Among the fatal, but rather rare complications, there are acute pancreatitis and the phenomenon of the "stone heart", which is essentially a reperfusion injury of the myocardium caused by rapid calcium overload. Hypercalcaemia can also trigger rhythm disturbances, hypertension, increase systemic vascular resistance, reduce diastolic compliance and impair relaxation of the myocardium due to excessive calcium intake into the cardiomyocytes, cause coronary vasospasm and aggravate ischaemic myocardial damage, impair arterial graft blood flow during aortocoronary and mammary coronary bypass surgery.

To date, there is a lack of data indicating clinical efficacy of calcium administration before separation from CPB. Therefore, we designed this randomized controlled trial to test the hypothesis whether calcium administration at termination of CPB will reduce the need for inotropic support at the end of surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •surgery under cardiopulmonary bypass
  • •valve or valve surgery + CABG
  • •age > 18 years
  • •signed informed consent

排除标准

  • •emergency surgery
  • •isolated aortic valve repair/replacement
  • •isolated CABG
  • •planned (before surgery) blood transfusion
  • •redo surgery
  • •known allergy to the study drug
  • •pregnancy
  • •current enrollment into another RCT (in the last 30 days)
  • •previous enrollment and randomization to ICARUS trial - liver cirrhosis (Child B or C)
  • •transfusion during CPB
  • •hypo- or hyperparathyreosis

研究组 & 干预措施

0,9% Sodium Chloride

Placebo Comparator

Participants randomly assigned to the placebo group will receive equivalent amount of placebo intravenously during separation from cardiopulmonary bypass

干预措施: 0.9% Sodium Chloride (Drug)

Calcium chloride

Experimental

Participants randomly assigned to the experimental group will receive 15 mg/kg of calcium chloride (bolus) intravenously during separation from cardiopulmonary bypass

干预措施: Calcium Chloride (Drug)

结局指标

主要结局

Inotropic support

时间窗: Intraoperatively

Number of patients requiring inotropic and/or vasopressor support started at any dose during the period starting at termination of CPB and ending at completion of surgery

次要结局

  • Vasoactive-inotropic score(Postoperative day 1)
  • CPB duration(intraoperatively)
  • ICU readmission(Postoperatively until hospital discharge)
  • Hospital stay(Postoperatively until hospital discharge)
  • Plasma Ca2+ concentration before and after drug administration(Intraoperatively)
  • Time spent in theatre after cardiopulmonary bypass(Intraoperatively)
  • Need for blood transfusion after surgery(Up to 30 day after randomization)
  • Internal mammary artery vascular resistance (if available)(Intraoperatively)
  • Myocardial infarction(Up to 30 day after randomization)
  • Type 1 and type 2 neurological complications(Up to 30 day after randomization)
  • Postoperative blood loss(Postoperative day 1)
  • Myocardial ischaemia on ECG after arrival to ICU(Postoperative day 1)
  • Concentration of alpha-amylase after surgery(Postoperative day 1)
  • Duration of inotropic support after surgery(30 days after surgery)
  • Duration of ventilation(Up to 30 day after randomization)
  • Duration of intensive care unit stay(Up to 30 day after randomization)

研究者

发起方
Meshalkin Research Institute of Pathology of Circulation
申办方类型
Network
责任方
Sponsor

研究点 (11)

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