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临床试验/CTRI/2025/07/090013
CTRI/2025/07/090013尚未招募4 期

Efficacy of Bupivacaine vs Bupivacaine with Dexamethsaone in Erector spinae block for postoperative pain in paediatric patients undergoing video assisted thoracoscopic surgeries

DR ASHISH ERRY1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年7月13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
50
试验地点
1
主要终点
To compare efficacy of Bupivacaine vs Dexamethasone with Bupivacaine in erector spinae block in pediatric patients undergoing VATS

研究概览

简要总结

It is a prospective, randomized, single blinded comparative study to compare the analgesic efficacy of dexamethasone as an adjuvant to bupivacaine versus bupivacaine in erector spinae block post operatively in pediatric patients undergoing VATS.

Parameters that will be compared between the two groups will be the duration of analgesia, time to rescue analgesia and number of rescue analgesia given.

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
1.00 Year(s) 至 10.00 Year(s)(—)
性别
All

入选标准

  • Patients ASA 1 & 2 Patients undergoing VATS.

排除标准

  • Patients m0re than 10 years of age Patients with coagulopathies ASA 3 & 4 Parents who did not give consent Patients allergic to either dexamethasone or bupivacaine.

结局指标

主要结局

To compare efficacy of Bupivacaine vs Dexamethasone with Bupivacaine in erector spinae block in pediatric patients undergoing VATS

时间窗: After giving erector spinae block FLACC score was used to asses postoperative pain and rescue analgesia given accordingly and time noted to compare the efficacy.

次要结局

未报告次要终点

研究者

发起方
DR ASHISH ERRY
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

erryash@gmail.com

DR DY PATIL VIDYAPEETH, PUNE

研究点 (1)

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