跳至主要内容
临床试验/CTRI/2021/02/030907
CTRI/2021/02/030907尚未招募1/2 期

Post operative analgesic requirement with or without sono-guided erector spinae plane block in patients undergoing abdominal surgery: A randomized, controlled interventional study, SMS Hospital, Jaipur

Dept of Anaesthesiology SMS Medical College and Attached Group of Hospitals1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2021年1月2日最近更新:

试验速览

阶段
1/2 期
状态
尚未招募
发起方
入组人数
80
试验地点
1
主要终点
To determine the difference in mean analgesic dose required post operative period in both groups

研究概览

简要总结

Regional anaesthesia is highly effective bothfor the surgical procedure and postoperative pain management. Abdominal surgeries can lead to significantpostoperative pain. In  these patients, different regional anesthesiatechniques play an important role in multimodal analgesia plans. Non-opioidanalgesia techniques are especially important in aging populations whencomorbidities are considered. Erector Spinae Plane block (ESPB), firstdescribed by Forero et al for analgesia in thoracic neuropathic pain hasalso been reported for the management of other causes of acute andpostoperative pain. In this study, we aim to determine thepostoperative analgesic effect of USG guided Thoracic ESPB (T-ESPB) in patientsundergoing abdominal surgery.

研究设计

研究类型
Interventional
分配方式
Other
盲法
Not Applicable

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • 1.Patients belonging to American Society of Anesthesiologists (ASA): Grade I: Without co-morbid conditions Grade II: Controlled co-morbid conditions Grade III : Poorly controlled co-morbid conditions 2.Weight 40-80 kg.

排除标准

  • 1.Patients not willing to participate in the study 2.H/O allergic reactions to local anesthetics 3.Patients on anticoagulant therapy and H/O coagulation disorders 4.Local infection at the proposed site of puncture for Erector Spinae Plane block 5.Chronic use of opioids or corticosteroids.

结局指标

主要结局

To determine the difference in mean analgesic dose required post operative period in both groups

时间窗: 12 hours and 24 hours

次要结局

  • To determine the time of first rescue analgesic in both groups.(12 hours , and every 1 hour thereafter upto 24 hours.)

研究者

发起方
Dept of Anaesthesiology SMS Medical College and Attached Group of Hospitals
申办方类型
Government medical college

研究点 (1)

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