临床试验/CTRI/2018/10/016120

CTRI/2018/10/016120尚未招募不适用

TO COMPARE THE EFFICACY OF INTRAOPERATIVE LANDMARK GUIDED ERECTOR SPINAE PLANE BLOCK VERSUS SUBCUTANEOUS INFILTRATION TECHNIQUE FOR POST OPERATIVE ANALGESIA IN PATIENTS UNDERGOING THORACOLUMBAR SPINE SURGERIES- A RANDOMISED CONTROLLED TRIAL

Ganga Hospital1 个研究点分布在 1 个国家目标入组 80 人开始时间: 2018年10月28日最近更新: 2018年10月20日

试验速览

阶段: 不适用
状态: 尚未招募
发起方: Ganga Hospital
入组人数: 80
试验地点: 1
主要终点: VAS SCORE

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

A prospective double blinded randomised control study to compare the efficacy of erector spinae block versus subcutaneous infiltration in patient undergong thoracolumbar surgeries.

patients will get either landmark guided erector spinae block or subcutaneous infiltration using 0.25%bupivacaine on either side of incision line at the end of surgery.

Postoperative pain assessment using VAS score and duration of the pain relief will be recorded and the total consumption of opioid.

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 60.00 Year(s)（—）
性别: All

入选标准

•Elective spine fusion surgery ASA I, II No neurological deficit.

排除标准

•Fracture spine patient Uncontrolled diabetes mellitus Neurological deficit.

结局指标

主要结局

VAS SCORE

时间窗: VAS Score every 2 hour for 24 hours | Duration Of Analgesia upto 24hours

DURATION OF ANALGESIA

时间窗: VAS Score every 2 hour for 24 hours | Duration Of Analgesia upto 24hours

次要结局

Consumption Of Opioid(Consumption Of Opioid over 24hours)

研究者

发起方

Ganga Hospital

申办方类型

Research institution and hospital

研究点 (1)

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