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临床试验/NCT05451381
NCT05451381已完成不适用

Vasopressor Requirements During Dexmedetomidine Sedation vs Propofol vs Their Combination (Dexmedetomidine and Propofol) Sedation in Patients After Cardiac Surgery

Anesthesia Research Group UA1 个研究点 分布在 1 个国家目标入组 356 人开始时间: 2017年8月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
356
试验地点
1
主要终点
vasopressor requirements

研究概览

简要总结

Most of the patients after cardiac surgery need sedation in the iCU. Sedation strategy could impact the incidence of vasopressor use.

详细描述

Sedating a patient is a complex process, especially after heart surgery. Sedation has a negative hemodynamic effect. This leads to a decrease in blood pressure and increases the frequency and dose of vasopressors used. The choice of drug for sedation may have an impact on reducing the frequency of use of vasopressor therapy. The goal of the research is compare three strategies: propofol ( sedative agent), dexmedetomidine ( selective α2-adrenergic receptor (α2-AR) agonist that is associated with sedative effect) and their combination for sedation after cardiac surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

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

入选标准

  • Multi vascular lesions of the coronary arteries according to coronary angiography;
  • Heart valve damage was confirmed by heart ultrasound, which is subject to surgical correction (aortic stenosis of III degree with a gradient on the aortic valve of more than 42 mmHg, aortic insufficiency III, mitral valve stenosis II-III, mitral regurgitation II-III)
  • Age of patients from 18-80 years;
  • Patient consent to participate in the study;
  • Women who have a negative pregnancy test and use effective contraception throughout the study and for 3 weeks after its completion, or women who are unable to have children (women who have undergone a hysterectomy (removal of the uterus) or tubal ligation, women with a clinical diagnosis of infertility) or are menopausal for more than 1 year (absence of menstruation for at least 12 months). Adequate methods of contraception include: surgical sterilization, double barrier method of contraception, local contraception;

排除标准

  • Refusal to participate;
  • Hypersensitivity to propofol, dexmedetomidine;
  • Prolonged mechanical ventilation in case of surgical complications (bleeding, inadequate perfusion of the myocardium);
  • Occurred ischemic stroke;
  • History of the ischemic stroke;
  • History of the neurodegenerative diseases;
  • History of the mental disorders;
  • Use of neuroleptics, antidepressants for the last 5 years;
  • History of the cardiac surgery in the past;
  • Patients with chronic pulmonary disease (GOLD 3-4)
  • Patients with asthma (moderate or severe),
  • Participation in any other clinical trial;
  • Gastric or duodenal ulcer with risk of bleeding;
  • Chronic renal failure (ClCr less than 50 ml / h)
  • Acute renal failure that occurred during surgery (ClCr less than 50 ml / h, or a decrease in the rate of diuresis to 0.1 ml / h in the first 4 hours after surgery and does not respond to diuretic therapy)
  • Chronic hepatic insufficiency if there are laboratory signs of hypo coagulation without the use of anticoagulant therapy (INR> 1.5)
  • If the patient has not stopped taking anticoagulants or antiplatelet agents in the preoperative period: warfarin 5 days before surgery, clopidogrel 5-7 days before surgery, xarelto / pradaxa 3 days before surgery),
  • History of the hematological disease;
  • Alcohol abuse in the anamnesis (3-4 times a week).
  • Condition after chemotherapy;
  • Pregnancy, lactation.

研究组 & 干预措施

Propofol group

Experimental

Patient sedation after cardiac surgery at the intensive care unit.

Sedation group (PR):

continuous infusion of propofol using a syringe pump at the dose of 1-1.5 mg / kg / h

干预措施: Propofol (Drug)

Dexmedetomidine group

Experimental

Patient sedation after cardiac surgery at the intensive care unit.

Sedation group Dexmedetomidine (DEX):

continuous infusion of Dexmedetomidine using a syringe pump at the dose of 0.5-1.0 mcg/ kg / h

干预措施: Dexmedetomidine (Drug)

Dexmedetomidine and propofol group

Experimental

Patient sedation after cardiac surgery at the intensive care unit.

Sedation group DEX+PR:

continuous infusion of propofol using a syringe pump at the dose of 0.5-1.5 mg / kg / h and dexmedetomidine 0.2-0.7 mcg\kg\h

干预措施: Dexmedetomidine and Propofol (Drug)

结局指标

主要结局

vasopressor requirements

时间窗: every hour during sedation(up to 12 hours)

incidence of cases of using norepinephrine. measurement tool is a fact of using that is marked as yes\\no in the check-list

dose of norepinephrine

时间窗: every hour during sedation (up to 12 hours)

measure the maximum dose of norepinephrine in mcg\\kg\\min to achieve mean arterial pressure 70 mmHg

次要结局

  • Length of stay in the ICU(before discharging from ICU to the ward ( up to 3 days))

研究者

发起方
Anesthesia Research Group UA
申办方类型
Other
责任方
Principal Investigator
主要研究者

Plechysta Yelyzaveta

chief of the anesthesia department

Anesthesia Research Group UA

研究点 (1)

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