CTRI/2017/10/010044尚未招募4 期
A prospective randomised comparative study to evaluate optimal induction and maintenance dose of propofol according to total body weight,lean body weight and ideal body weight.
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
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 undergoing elective laparoscopic surgery with BMI between 30 and 40, ASA 1and 2 under general anaesthesia for a minimum duration of 30 minutes to maximum of 3 hours
排除标准
- •1.History of significant cardiac pulmonary, liver or renal disease.
- •2. Patient scheduled for awake bronchoscopic intubation.
- •3. Previous history of cerebrovascular accident, other neurological disorders and those on long term drugs affecting CNS (chronic BZDâ??s/ opioids)
- •4. Allergy to propofol.
- •5. Patients with significant hemodynamic changes intraoperatively, fall of Mean arterial blood pressure by more than 20% of baseline,intraoperative entropy of more than 60 for more than 10 minutes and need to add inhalational agent will be excluded.
- •6) patients refusal to be included in the study
研究者
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