CTRI/2019/02/017641尚未招募未知
A study to ascertain the target concentration of Propofol to achieve bispectral index guided sedation for monitored anaesthesia care using target-controlled infusion
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- A
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
入选标准
- •Patients belonging to American Society of Anaesthesiologists physical status grade I and II, aged between 18 to 70 years, scheduled to undergo surgery under spinal/epidural anaesthesia with an expected duration of 1-3 hrs.
排除标准
- •1. Patient refusal
- •2. Hepatic insufficiency
- •3. Renal insufficiency
- •4. Pulmonary disease
- •5. History of chronic drug use that could affect
- •the central nervous system
- •6. Significant hemodynamic instability
- •7. Known allergy to propofol
- •8. Pregnancy
- •9. Impaired hearing
- •10. Neurological deficits or a Glasgow Coma
- •Scale score under 15
- •11. Known or predicted difficult airway
- •12. History of neurologic or psychiatric
研究者
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