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临床试验/CTRI/2018/03/012732
CTRI/2018/03/012732招募中Unknown

Comparison of tramadol and dexmedetomidine in treatment of post neuraxial anaesthesia shivering

Akanksha Bansal1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2017年1月1日最近更新:

试验速览

阶段
Unknown
状态
招募中
发起方
入组人数
100
试验地点
1
主要终点
control of shivering

研究概览

简要总结

Shivering after neuraxial blockade should be managed efficiently to reduce its complications. Thus this study would conclude the better drug which can be used in cases of shivering. Also the study will compare the side-effects of the treatment drug and the rate of recurrence after giving the treatment, ultimately reducing the patient discomfort.

AIM-

The purpose of this study is to compare Dexmedetomidine 0.5 μg/kg with that of Tramadol 0.5 mg/kg, both diluted in 10 ml NS given as IV infusion in 1 minute, in the treatment of shivering in patients undergoing elective surgery under spinal anaesthesia.

OBJECTIVE-

1.To assess the efficacy, potency and side-effects of Tramadol in treatment of shivering

2.To assess the efficacy, potency and side-effects of Dexmedetomidine in treatment of shivering

3.To compare the efficacy, potency and side-effects of both the drugs

研究设计

研究类型
Interventional
分配方式
Not Applicable
盲法
Not Applicable

入排标准

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

入选标准

  • ASA Grade I and II
  • Patients admitted for lower abdominal and lower limb surgeries.

排除标准

  • Patients with cardiopulmonary disease, hepatic disorder, respiratory and neurological disorder.
  • Allergy to the study drugs
  • Those with an initial heart rate < 50 beats/minute
  • Systolic blood pressure < 100 mmHg
  • Patient on narcotics or any other sedatives which alter the thermoregulation
  • Patients with recent history of febrile illness and those with history of malignant hyperthermia.
  • Contraindication to regional anaesthesia.

结局指标

主要结局

control of shivering

时间窗: 5 minutes

次要结局

  • Recurrence of shivering(3 months)

研究者

发起方
Akanksha Bansal
申办方类型
Other [self]

研究点 (1)

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