A Prospective observational research comparing the recovery profiles of patients undergoing non-abdominal procedures who received propofol using Schneider(TIVA) pharmacokinetics model versus manual infusion.
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 54
- 试验地点
- 1
- 主要终点
- Induction time at start of surgery.
研究概览
简要总结
Patients will be shifted inside the operating room and baseline monitors such as ECG , Bloodpressure ,pulse oximeter shall be connected and baseline parameters will be noted . A 18g Intravenous cannula will be placed . General anesthesia will be induced and maintained by either manual syringe pump or target- controlled pump using propofol . Depth of anesthesia shall be monitored using bispectral index monitor (BIS). Depending upon the BIS value , the dose of propofol will be adjusted. At the end of surgery patient’s recovery will be noted with modified Aldrete score.
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •American society of anaesthesiologist physical status I and II.
- •Patients undergoing non-abdominal surgeries.
排除标准
- •Age below 18 years and above 60 years.
- •ASA III and above.
结局指标
主要结局
Induction time at start of surgery.
时间窗: Induction time at start of surgery. | extubation time at end of surgery.
extubation time at end of surgery.
时间窗: Induction time at start of surgery. | extubation time at end of surgery.
次要结局
- modified Aldrete score for recovery - end of surgery.(modified aldrete score for recovery - end of surgery)
研究者
Keerthana M
saveetha medical college and hospital.