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临床试验/CTRI/2024/11/076745
CTRI/2024/11/076745尚未招募2/3 期

Comparison of Nebulised Ropivacaine 0.75 percent Versus Nebulised Dexmedetomidine and Nebulised lignocaine 4 percentin patients undergoing surgery under General Anesthesia.

Aysath nuhaimah1 个研究点 分布在 1 个国家目标入组 105 人开始时间: 2025年2月23日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
入组人数
105
试验地点
1
主要终点
Monitor the hemodynamic changes in patients received ultrasonic nebulisation 4 % lignocaine at 10 minutes before and after nebulisation, 10 min, 20 minutes , 30 minutes till 120 minutes after intubation

研究概览

简要总结

This is a prospective, comparative study to monitor the hemodynamic changes in patients received nebulisation lignocaine 4%, dexmedetomidine 1 microgram /kg  at the time of intubation , extubation and any cough response.

The response at noted in tabular form and being observed

研究设计

研究类型
Interventional
分配方式
Na
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • ASA grade I and II
  • Non- hypertensive 3.Non obese 4.MPC I and II 5.Surgeries lasting for at least upto 2 hours and not beyond 4 hours.
  • Elective surgeries.

排除标准

  • 1.Patients who refused to participate in study 2.patients age is less than 18 and not more than 60 years.
  • Patients with nasogastric tube.
  • 4.Contraindication for the use of nitrous oxide.
  • 5.Mallampati classification III and IV 6.hypertensive patients 7.ASA III AND IV 8.Patients with history of allergy to dexmedetomidine.
  • 9.Daycare surgeries.
  • Patients with difficult airway where the anticipated duration of laryngoscopy exceeded 15 seconds.
  • Emergency surgeries.’ 12.Patients with history of cardiac,liver or renal disorders.

结局指标

主要结局

Monitor the hemodynamic changes in patients received ultrasonic nebulisation 4 % lignocaine at 10 minutes before and after nebulisation, 10 min, 20 minutes , 30 minutes till 120 minutes after intubation

时间窗: Observed assessed by 12 weeks

Monitor the hemodynamic changes of patients received ultrasonic nebulisation of dexmedetomidine 1 micro gram per kg at 10 minutes before and after nebulisation.

时间窗: Observed assessed by 12 weeks

10 minutes, 20 minutes, 30 minutes till 90 minutes after intubation.

时间窗: Observed assessed by 12 weeks

Monitor hemodynamic changes in patients received ultrasonic nebulisation of 0.75 % ropivacaine at 10 minutes before and after nebulisation.

时间窗: Observed assessed by 12 weeks

10 minutes, 20 minutes till 90 minutes after intubation.

时间窗: Observed assessed by 12 weeks

次要结局

  • To compare the hemodynamic parameters of nebulised ropivacaine versus nebulised lignocaine versus nebulised dexmedetomidine at extubation(With 24 hours.)

研究者

发起方
Aysath nuhaimah
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Aysath nuhaimah

B.j medical college , Sassoon hospital

研究点 (1)

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