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临床试验/NCT07798089
NCT07798089尚未招募1 期

Propofol-Dexmedetomine Adjunction in Balanced Anesthesia for Minimally Invasive Cardiac Valve Surgery :Effect on Anesthetic Consumption ,Perioperative Outcomes,and Early Recovery : Randomized Controlled Trial

Kafrelsheikh University0 个研究点目标入组 60 人开始时间: 2026年9月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
尚未招募
入组人数
60
主要终点
total intraoperative isoflurane consumption between propofol dexmedetomidine anesthesia and propofol anesthesia alone under entropy-guided anesthesia

研究概览

简要总结

Propofol-Dexmedetomidine Adjunction in Balanced Anesthesia for Minimally Invasive Cardiac Valve Surgery: Effects on Anesthetic Consumption, perioperative outcomes, and Early Recovery

详细描述

This prospective, randomized, double-blind study was conducted to evaluate the effect of dexmedetomidine as an adjunct to propofol-based anesthesia in patients undergoing minimally invasive cardiac valve surgery. Patients were randomly allocated to receive either dexmedetomidine or placebo in addition to standard propofol-based anesthesia. The primary outcome was total propofol consumption during surgery. Secondary outcomes included intraoperative hemodynamic parameters, anesthetic and recovery characteristics, and postoperative outcomes.

研究设计

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

入排标准

年龄范围
25 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • patients belonging to American Society of Anesthesiologists (ASA) class I or II
  • patients scheduled for minimally invasive cardiac valve surgery.

排除标准

  • patient more than 60 years
  • patients having neurological/psychological disorders,
  • patient having severe systemic disorders (renal/hepatic dysfunction and severe respiratory disorder),
  • patient with history of allergy to the study drugs,
  • patient with left ventricular ejection fraction < 40%,

研究组 & 干预措施

Propofol group (Group P) (control group)

Active Comparator

干预措施: Propofol (Astra-Zeneca) (Drug)

Propofol dexmedetomidine group (Group PD)

Active Comparator

干预措施: propofol and dexmetomidine (Drug)

结局指标

主要结局

total intraoperative isoflurane consumption between propofol dexmedetomidine anesthesia and propofol anesthesia alone under entropy-guided anesthesia

时间窗: Time Frame: From induction of anesthesia until discontinuation of anesthesia; total isoflurane consumption will be recorded at the end of surgery.

Total intraoperative isoflurane consumption Description: The total amount of isoflurane consumed during anesthesia will be compared between patients receiving propofol-dexmedetomidine anesthesia and those receiving propofol anesthesia alone under entropy-guided anesthesia. Isoflurane consumption will be assessed from induction of anesthesia until discontinuation of anesthesia and measured as the total volume consumed. (ML\\MIN)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Donia Hany Saad

Lecturer of Anesthesiology and Surgical Intensive Care

Kafrelsheikh University

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