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临床试验/CTRI/2024/07/070975
CTRI/2024/07/070975尚未招募3 期

Erector Spinae Plane Block supplementation to General anaesthesia in abdominolumbar surgeries for postoperative quality of recovery

Peoples Hospital1 个研究点 分布在 1 个国家目标入组 110 人开始时间: 2024年7月29日最近更新:

试验速览

阶段
3 期
状态
尚未招募
入组人数
110
试验地点
1
主要终点
Quality of recovery

研究概览

简要总结

to compare the effect of erector spinae plane block with levobupivacaine in patients undergoing abdomino lumbar surgeries vs a control group undergoing general anesthesia with erector spinae plane block with normal saline and these patients will be evaluated for post operative quality of recovery till the point of discharge by Qor 15 scale

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant 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

  • ASA grade 1 and 2.

排除标准

  • ASA grade 3 and 4 not willing to give consent allergy to levobupivacaine patient with spinal deformity psychiatric disorder chronic neurological disease pregnant and lactating female emergency or trauma cases.

结局指标

主要结局

Quality of recovery

时间窗: Patients will be assessed for quality of recovery using QoR15 scale for 240 minutes

次要结局

  • haemodynamic parameters(240 minutes)

研究者

申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

DR ASHWIN KRISHNAN NAIR

Peoples Hospital

研究点 (1)

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