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临床试验/CTRI/2025/10/095811
CTRI/2025/10/095811尚未招募不适用

Assessing the Spread of Local Anaesthetic Injection Bupivacaine 0.25 percent(30ml) Using Radiocontrast Dye in Pericapsular Nerve Group (PENG) Block for Hip Surgeries – A Case Series

Sapthagiri institute of medical science and research centre1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2025年10月20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
10
试验地点
1
主要终点
To determine the spread of injection Bupivacaine 0.25%, 30ml in myofascial plane in ultrasound guided PENG block in elective hip surgeries in tertiary hospital for post op analgesia in terms of VAS score and ease of positioning for spinal anaesthesia

研究概览

简要总结

This is a prospective observational case series designed to evaluate the anatomical spread and clinical efficacy of the Pericapsular Nerve Group (PENG) block in patients undergoing elective hip surgeries. Severe pain in hip fracture patients often makes positioning for subarachnoid block (SAB) difficult. The PENG block is a novel ultrasound-guided regional anaesthesia technique targeting the articular branches of the femoral, obturator, and accessory obturator nerves, potentially providing superior analgesia.

In this study, 10 adult patients, above 18 years, scheduled for hip surgeries under spinal anaesthesia will receive an ultrasound-guided PENG block with 30 ml of 0.25 bupivacaine mixed with iohexol radiocontrast dye (OMNIPAQUE). The injectate spread will be visualised using C-ARM imaging at 5, 10, and 20 minutes after injection.

Primary outcome: Anatomical spread pattern of the injectate as seen on C-ARM imaging and Reduction in pain intensity measured by Visual Analogue Scale (VAS) at baseline, immediately post-block, and at 10, 15, and 20 minutes and Ease of positioning for SAB graded on a 0–3 scale.

The findings will help understand the spread characteristics of the PENG block, optimise block techniques, and provide baseline data for future larger controlled trials.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 90.00 Year(s)(—)
性别
All

入选标准

  • Elective hip surgery under spinal anaesthesia.
  • ASA Physical Status I and II 3)Written informed consent provided.

排除标准

  • Allergy to local anaesthetics or radiocontrast agents.
  • Coagulopathy or ongoing anticoagulant therapy.
  • Local infection at injection site.
  • Pregnant or lactating women.
  • Acute and chronic kidney disease patients.

结局指标

主要结局

To determine the spread of injection Bupivacaine 0.25%, 30ml in myofascial plane in ultrasound guided PENG block in elective hip surgeries in tertiary hospital for post op analgesia in terms of VAS score and ease of positioning for spinal anaesthesia

时间窗: Spread is assessed at 0min, 5min, 10 min, 15 min and 20min along with ease of positioning and VAS score

次要结局

未报告次要终点

研究者

发起方
Sapthagiri institute of medical science and research centre
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Ahish Bhat K

Sapthagiri Institute of Medical Sciences and Research Centre

研究点 (1)

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