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临床试验/CTRI/2024/12/078305
CTRI/2024/12/078305尚未招募4 期

Analgesic Efficacy of Ultrasound Guided Costotransverse Block in Paediatric patients undergoing Video Assisted Thoracoscopic Surgery: A Randomised Controlled Trial

All India Institute of Medical Science, Patna1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年1月1日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
40
试验地点
1
主要终点
To evaluate the 24-h postoperative opioid consumption per kg body weight

研究概览

简要总结

Video-assisted thoracoscopic surgery is a commonly done procedure in Paediatric patients.

These patients experience moderate to severe pain postoperatively increasing the risk of postoperative

complications and delaying their recovery.

Conventional analgesics like opioids have systemic adverse effects, insufficient pain alleviation and

delayed recovery. This has led to the advent of locoregional analgesic techniques like ultrasound

(USG) paravertebral block (PVB), which blocks both the dorsal and ventral rami providing adequate

pain relief. However this block is accompanied by complications like hematoma, hypotension and

pneumothorax. Lately US guided costotransverse block (CTB) has been described as a peri PVB where

the drug is deposited above superior costotransverse ligament. Its use has been described in adult

breast and Paediatric cardiac surgeries.

The purpose of this study is to investigate the costotransverse block’s analgesic effectiveness in

Paediatric VATS patients. This study aims to provide insight into the possible advantages of

incorporating this method into Paediatric thoracic surgery procedures.

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
1.00 Year(s) 至 14.00 Year(s)(—)
性别
All

入选标准

  • Patients aged 1 to 14 years scheduled for Video Assisted Thoracoscopic Surgeries.

排除标准

  • Parent/patient refusal to participate in the study Patients with coagulation disorders.
  • Patients hypersensitive to study medications.
  • Patients with developmental or mental delay.
  • Skin lesions or infection at the planned site of needle insertion Congenital vertebral anomalies Patients planned for postoperative ventilation.

结局指标

主要结局

To evaluate the 24-h postoperative opioid consumption per kg body weight

时间窗: From the end of surgery to 24 hours postoperatively

次要结局

  • To evaluate postoperative pain scores using the FLACC/NRS scale(30 minutes,)
  • To evaluate intraoperative fentanyl consumption(from the time of administration of block to the end of the surgery)
  • To evaluate side effects like vomiting, respiratory depression and sedation using(POSS scale)
  • Time to 1st rescue analgesia administration.(from the time of administration of block to the first need of use of analgesic administration)

研究者

发起方
All India Institute of Medical Science, Patna
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Naveen V

AIIMS PATNA

研究点 (1)

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