跳至主要内容
临床试验/CTRI/2020/02/023640
CTRI/2020/02/023640尚未招募不适用

A Randomised Controlled Trial to assess the postoperative analgesic efficacy of Fascia Iiliaca Block Versus Pericapsular Nerve Group (PENG)Block in patients undergoing hip fixation surgery

Lady Hardinge Medical College1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2020年2月29日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
80
试验地点
1
主要终点
1. Mean NRS Score at 0,4,8,12, 24 hours postoperatively in patients at rest and in movement

研究概览

简要总结

Hip fracture is a common orthopedic emergency in the elderly and is associated with significant morbidity and mortality, surgical reductions and fixations are the definitive treatments in most patients. Adequate pain relief is essential in the postoperative period .  Initially intravenous patient controlled analgesia and epidural analgesia were used . these have been replaced by various peripheral nerve blockade techniques ; these include lumbar plexus block , psoas compartment block , femoral nerve block and so on . Recently fascia iliaca block and (Pericapsular Nerve Group ) PENG block have been proposed for the same ,but there has been no comparative study regarding the two blocks . These peripheral nerve blocks have been found to be associated with reduced motor blockade , early ambulatory outcomes , adequate analgesia  and decreased requirement of opioids .

This study is a randomized controlled trial to assess the efficacy of fascia iliaca and PENG block in the postoperative period. The selection of the patients for the block will be done by computer generated random table and   both the blocks will be given preoperatively  and catheter will be placed at the site of the block and infusion pumps containing the drugs will be attached to the catheter. The surgery will be done under spinal anaesthesia and the catheter will be placed for 48 hours postoperative duration.

Following observations will be made

  1.  Mean NRS ( Numerical Rating Scale) score at 0 , 4,8,12, and 24 hours postoperatively

2. Change in NRS score while positiong for spinal anaesthesia

3. Mean dosage of 24 hours postopearive analgesic requirement

4. Proportion  of catheter and drug related complications

Data will be collected and compiled in an excel sheet and will be analyzed statistically .

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant, Investigator and Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • •AGE> 18 Years
  • •Patients planned for hip fixation surgery under spinal anaesthesia.

排除标准

  • •Patient’s refusal
  • •Any known drug allergies.
  • •Contraindication to nerve block like coagulopathy, bleeding diathesis and local infections.

结局指标

主要结局

1. Mean NRS Score at 0,4,8,12, 24 hours postoperatively in patients at rest and in movement

时间窗: 1. 0,4,8,12,24 hours postoperatively

次要结局

  • 1.Change in NRS score while positioning for spinal anaesthesia(2. Mean dosage of 24 hours postoperative analgesic requirements)

研究者

申办方类型
Government medical college

研究点 (1)

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