CTRI/2023/06/054006尚未招募Unknown
a comparative study of intravenous v/s nebulised dexmedetomidine for attenuation of pressor response to laryngoscopy & endotracheal intubation
Somya Pareek0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 发起方
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
- •1.ASA grades 1 & 2 (American Society of Anesthesiologists physical status)
- •2.Age group 18- 65 years
- •3.Either gender
- •4.Patients scheduled for elective surgery under general anaesthesia with endotracheal intubation
- •Patients fulfilling the above criteria consenting to participate in the study.
排除标准
- •1.Patient refusal.
- •2.Patients less than 18 years and more than 65 years of age.
- •3.Patients scheduled for general anaesthesia without endotracheal intubation such as mask ventilation, use of laryngeal mask airways, sedation, monitored anaesthetic care, or surgery duration more than 90mins.
- •4.Patients coming for surgery under regional anaesthesia.
- •5.Patients belonging to ASA grade >= III.
- •6.Patients undergoing emergency surgeries.
- •Obese individuals (body mass index > 30 kg/m2)
- •7.Patients with known or unanticipated difficult intubation and those requiring more than 15secs or two attempts at laryngoscopy.
- •8.Patients with arrythmias.
- •9.Patients with known allergy to dexmedetomidine, and those on anti-hypertensive medications or preoperative drugs that could be potential confounders (clonidine, gabapentin, pregabalin, steroids)
研究者
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