跳至主要内容
临床试验/CTRI/2025/11/097565
CTRI/2025/11/097565尚未招募Unknown

"To Evaluate Efficacy of Dexmedetomidine for Reducing Sucicnylcholine Induced Myalgia in Patients undergoing Electro convulsive Therapy."

Dhiraj Hospital Sumandeep vidyapeeth1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年12月15日最近更新:

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
100
试验地点
1
主要终点
This prospective study will help us to evaluate the efficacy of low dose intravenous Dexmedetomidine in reducing fasciculations and myalgia due to sucicnylcholine during electro convulsive therapy.

研究概览

简要总结

In the present study we will be comparing the efficacy of low dose of intravenous Dexmedetomidine (0.25 mcg/ kg) diluted in 100 ml Normal Saline for reducing incidence and severity of sucicnylcholine induced myalgia and fascination and optimization of hemodynamics in patients undergoing electro convulsive therapy.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Patients willing to sign informed consent.
  • Patient belonging to ASA physical status 1 and
  • Patients undergoing Electroconvulsive therapy.

排除标准

  • Patients unwilling to participate in study.
  • Patient with BMI more than 30 kg/m
  • Patient who are deaf or incapable of understanding the language.
  • Patients with history of allergy to an adrenergic agonist.
  • Pregnancy and lactating women.

结局指标

主要结局

This prospective study will help us to evaluate the efficacy of low dose intravenous Dexmedetomidine in reducing fasciculations and myalgia due to sucicnylcholine during electro convulsive therapy.

时间窗: This prospective study will help us to evaluate the efficacy of low dose intravenous Dexmedetomidine in reducing fasciculations immediately after giving Sccinylcholine and myalgia due to sucicnylcholine after 60 minutes of electro convulsive therapy.

次要结局

  • Effect of Dexmedetomidine in attenuating blood pressure & heart rate during electro convulsive therapy.(At Base line, 5 min after drug intervention, During ECT, 3 min, 5 min, 10 min, 20 min, 30 min after ECT)

研究者

发起方
Dhiraj Hospital Sumandeep vidyapeeth
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

DR SUCHETA SUHAS DOSHI

Smt Bhailal Kothari Shah Medical Institute and Research Centre Vadodara, Gujarat.

研究点 (1)

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