跳至主要内容
临床试验/CTRI/2026/01/100912
CTRI/2026/01/100912
尚未招募
4 期

Ultrasound guided erector spinae plane block vs fascia iliaca compartment block for post-operative analgesia in patients undergoing surgery for femur fractures: A Randomised Clinical Trial.

Dr Neha Chajgotra1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2026年2月1日最近更新:

概览

阶段
4 期
状态
尚未招募
发起方
Dr Neha Chajgotra
入组人数
80
试验地点
1
主要终点
1) Severity of pain using Visual Analog Scale ( VAS)

概览

简要总结

This study is a randomised, parallel group, clinical trial comparing the effectiveness of two blocks

i.e ultrasound guided Erector Spinae plane block versus fascia iliaca compartment block for

postoperative analgesia in patients undergoing femur fracture surgeries, as measured by duration of

analgesia and pain score in 24 hours following surgery. The primary outcome of the study is to

record the severity of pain using visual analog scale and time to request of first analgesia i.e

the time elapsed between the end of surgery to 1st dose of analgesia. The secondary outcome is

to see the total no. of analgesic doses of opioids and NSAIDs in 24 hours following surgery and to

see any side effects like nausea, vomiting and shivering occurring after the procedure

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 80.00 Year(s)(—)
性别
All

入选标准

  • patients between age group of 18 years to 80 years who are undergoing femur fracture fixation 2) ASA class 1 -3 3) patients who are willing to participate and provide a willing written informed consent.

排除标准

  • patients with any chronic medical illness 2) history of any bleeding disorders 3) patients allergic to any of these drugs 4) history of chronic opioid use 5) history of cognitive impairment 6) local infection at site.

结局指标

主要结局

1) Severity of pain using Visual Analog Scale ( VAS)

时间窗: Severity of pain using VAS at | 1,2,6,12 and 24 hours after surgery

2) Time to 1st request of analgesia

时间窗: Severity of pain using VAS at | 1,2,6,12 and 24 hours after surgery

次要结局

  • 1) Total number of analgesic doses of opioids and NSAIDS in 24 hours following(surgery)

研究者

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

Dr Neha Chajgotra

GMC Kathua

研究点 (1)

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