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临床试验/CTRI/2023/04/052079
CTRI/2023/04/052079招募中不适用

Comparison of Pericapsular Nerve Group (PENG) Block versus Supra-Inguinal Fascia Iliaca (SIFI) Block for post-operative analgesia in Hip surgeries.

Dayanand Medical College and Hospital1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年10月5日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
60
试验地点
1
主要终点
For PRIMARY OUTCOME: Postoperative pain will be measured using VAS pain scores at 24 hours at rest in both the groups.

研究概览

简要总结

Hip procedures are common orthopedic surgeries performed routinely and are associated with significant amount of pain. Adequate analgesia is very crucial post-operatively to enhance dynamic pain relief, early patient recovery, reduced hospital stay, prevention of readmissions along with overall improved patient satisfaction to recovery. Peripheral nerve blocks have the advantage of potent analgesia, minimal systemic complications which are associated with central neuraxial blockades and less motor blockade, therefore leading to early patient recovery and overall better outcomes. A prospective, double-blinded randomized study will be conducted on 60 adult patients, ASA- I to III undergoing orthopedic surgeries for hip fractures, under sub-arachnoid block in which they will be randomly allocated to either group A which will receive 30ml of 0.2% Ropivacaine with 4mg dexamethasone USG-guided pericapsular nerve group (PENG) block or to group B which will receive 30ml of 0.2% Ropivacaine with 4mg dexamethasone USG-guided supra-inguinal fascia iliaca (SIFI) block. The primary outcome is comparing VAS scores at rest at 24 hours in both the groups. The secondary outcome is functional mobility at 24 and 48 hours postoperatively by assessing the quadriceps muscle strength, maximum weight bearing possible at 24 hours and 48 hours post-operatively, time to need for first rescue analgesia, total opioid consumption in first 24 hours along with overall patient satisfaction to recovery and surgeon’s satisfaction to overall pain management in both the groups.

研究设计

研究类型
Interventional
分配方式
Other
盲法
Participant and Investigator Blinded

入排标准

年龄范围
40.00 Year(s) 至 85.00 Year(s)(—)
性别
All

入选标准

  • Patients aged 40-85 years of age
  • ASA Physical status I, II, III
  • Electively scheduled for hip surgeries.

排除标准

  • Known allergy to study drugs
  • Contraindication to neuraxial blockade or peripheral nerve blocks
  • Chronic opioid use
  • Diabetic neuropathy
  • Infection at the site of block.

结局指标

主要结局

For PRIMARY OUTCOME: Postoperative pain will be measured using VAS pain scores at 24 hours at rest in both the groups.

时间窗: The patients will be monitored hourly for the first 4 hours, 2 hourly for the next 4 hours and then every 4 hourly till 24 hours post-operatively.

次要结局

  • For SECONDARY OUTCOMES:(• functional mobility will be)

研究者

发起方
Dayanand Medical College and Hospital
申办方类型
Private medical college

研究点 (1)

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