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临床试验/CTRI/2024/11/076848
CTRI/2024/11/076848尚未招募不适用

“Comparision of opioid free anaesthesia by using bilateral retrolaminar block with conventional opioid based anaesthesia for improved recovery in patients undergoing lumbar laminectomy: A randomised controlled interventional study”

Dr Dhamodharan M1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年11月21日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
To compare the recovery time

研究概览

简要总结

The study aims for comparision of opioid free anaesthesia by using bilateral retrolaminar block with conventional opioid based anaesthesia for improved recovery in patients undergoing lumbar laminectomy

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator 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

  • Body mass index (BMI): 18–28kg/m2 American Standards Association (ASA) grade I–II; Patients undergoing elective surgeries of lumbar laminectomy.

排除标准

  • Patient refusal 2) History of allergy to study drugs; 3) Pregnant and lactating females 4) Lower limb weakness with motor or sensory disturbances 4) History of chronic pain or long-term use of psychotropic drug or substance abuse.

结局指标

主要结局

To compare the recovery time

时间窗: assessed postoperatively at the time of baseline during extubation

次要结局

  • tracheal extubation time(assessed at the time of baseline)
  • discharge from PACU(assessed at the time of 15 mins from baseline)
  • pain score at rest & movement using VAS(timed intervals at every half an hour from baseline to 24 hours postoperatively)
  • duration of analgesia(assessed every half an hour from the time of baseline)
  • total tramadol consumption(assessed for 24hours of postoperative period from baseline)
  • postoperative side effects such as nausea & vomiting(during 24hours of postoperative period from baseline)

研究者

发起方
Dr Dhamodharan M
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Dhamodharan M

Dr S N medical college

研究点 (1)

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