跳至主要内容
临床试验/CTRI/2024/06/068790
CTRI/2024/06/068790尚未招募2 期

Analgesic efficacy of combining pericapsular nerve group block (PENG) with lateral femoral cutaneous nerve block (LFCN) in fractured hip surgeries under spinal anaesthesia - a randomised double blind trial.

Kalinga Institute of Medical Sciences1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2024年7月1日最近更新:

试验速览

阶段
2 期
状态
尚未招募
入组人数
80
试验地点
1
主要终点
The time required to request for the 1st rescue analgesia with tramadol in minutes.

研究概览

简要总结

Orthopaedic surgeries, especially those around the hip joint are extremely painful for the patient as it involves extensive soft tissue, muscles, ligaments and bone dissection. 

The Pericapsular nerve group block is an ultrasound-guided approach for the blockade of the articular branches of the femoral, obturator and accessory obturator nerves that provide sensory innervation to the anterior hip capsule.

Most hip surgeries require a lateral incision, which involves the cutaneous supply by the branches of the Lateral Femoral Cutaneous Nerve (LFCN).

Hence, we will conduct a double blinded, randomized study to compare PENG block with a combination of PENG block and LFCN block for efficacy of analgesia in fractured hip surgery.

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 60.00 Year(s)(—)
性别
All

入选标准

  • All willing and consenting participants, American Society of Anaesthesiologist (ASA) physical status I-III.

排除标准

  • Participants with coagulopathy , cardiovascular disease , psychiatric illness, speech and hearing impairment, morbidly obese and those allergic to anaesthetic drugs.

结局指标

主要结局

The time required to request for the 1st rescue analgesia with tramadol in minutes.

时间窗: at 0 minutes , 30 minutes , 60 minutes, 90 minutes

次要结局

  • The Numerical Rating Scale (NRS) for Pain recorded post block at rest and upon movement i.e. by passively lifting the limb 15° above the resting level.(30 minutes)
  • Ease of spinal Positioning score assessed using a four-point scale.(30 MINUTES)
  • Total tramadol consumption.(24 HOURS)
  • Any complications or adverse effect would be measured.(24 HOURS)
  • Patient satisfaction score.(24 hours)

研究者

申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Ujjaini Ray

Kalinga Institute of Medical Sciences

研究点 (1)

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