跳至主要内容
临床试验/CTRI/2026/04/107562
CTRI/2026/04/107562尚未招募不适用

To compare the efficacy of ultrasound guided modified thoracolumbar Interfascial plane block and lumbar-erector spinae plane block in lumbar spine surgeries - A randomised comparative study

Dr Angezna dharma1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2026年4月6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
50
试验地点
1

研究概览

简要总结

We aim to study and compare the efficacy of ultrasound guided modified thoracolumbar interfascial plane block and lumbar erector spinae plane block in lumbar spine surgeries. Patients will be divided into two groups with the help of the randomisation technique.

Patients falling under Group A will undergo a mTLIP block bilaterally with a dose of 0.5 percent ropivacaine 15 mL and 100 mcg dexmedetomidine on each side after induction of patient under general anaesthesia at IGMC,Shimla while patients belonging to Group B will receive Lumbar Erector Spinae Plane (L-ESP) block with of a mixture of 15 ml of 0.5 percent Ropivicaine and 100mcg dexmedetomidine on each side after induction with GA at IGMC, Shimla. After the completion of surgery the patient will be extubated and transferred to the post- anaesthesia care unit .At PACU ,the patient’s visual analog score (VAS) will be assesed . Time zero will be the pain status of the patient after shifting the patient to the Post anaesthesia care unit. Patient satisfaction score will be observed after a period of 48 hours and compared among the two groups.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
30.00 Year(s) 至 75.00 Year(s)(—)
性别
All

入选标准

  • Patients age from 30 to 75 yrs. ASA physical status I.
  • lll Elective lumbar spine surgeries.

排除标准

  • Patients with known allergy to local anaesthetics.
  • Patient with previous lumbar spine surgeries.
  • Patients with a history of coagulopathy or on anticoagulant and anti-platelet drugs.
  • Polytraumatic patient with head injury or in shock.
  • Patients with infection at the site of block Patients who refuse to participate in study.
  • Pregnant women.
  • Patients with chronic opioid use or psychiatric illness.
  • Patient receiving ketamine at the time of induction.

研究者

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

Angezna Dharma

Indira Gandhi medical college

研究点 (1)

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