跳至主要内容
临床试验/CTRI/2023/03/050508
CTRI/2023/03/050508尚未招募不适用

Analgesic efficacy of erector spinae plane block in pediatric patients - Our experience in a tertiary care hospital

St Johns Medical College and Hospital1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2023年3月15日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
50
试验地点
1
主要终点
Duration of analgesia

研究概览

简要总结

This is a prospective ,observational,descriptive study which aims to determine the analgesic effects of erector spinae plane block (ESPB)in pediatric patients aged between 2-7yrs posted for abdominal and lower limb surgeries.

The primary objective of the study is to assess the duration of analgesia provided by ESPB (time to first request of rescue analgesic postoperatively) and secondary objectives are to assess frequency of rescue analgesics used and total number of rescue analgesics utilized during the intraoperative and postoperative period.

All children posted for abdominal ,inguinal,hip and femur surgeries fulfilling the inclusion criteria will receive  ESPB after general anesthesia with dose of 0.5ml/kg with a maximum dose of 2mg /kg of 0.25% bupivacaine with dexamethasone 100mcg/kg at the level of lumbar vertebrae appropriate for the case.

Intraoperatively, heart rate (HR) ,mean arterial pressure (MAP) will be monitored every 15 minutes .If the vitals rises more than 20 percent of baseline values then iv rescue analgesics (fentanyl-0.5mcg/kg) will be given.

Postoperatively the duration of analgesia provided by ESPB will be assessed by assessing revised FLACC score  at 10 minutes, 20 minutes, 2 hours, 6 hours, 12 hours, 24 hours.  If FLACC >3 then iv paracetamol will be given(15mg/kg) as rescue analgesic and if FLACC >5 then iv pethidine will be given (0.5mg/kg).

Frequency of rescue analgesics and total doses of rescue analgesics given for a period of 24 hours during the postoperative period will be observed.

Descriptive and inferential statistics will be calculated to provide statistical significance.

研究设计

研究类型
Observational

入排标准

年龄范围
2.00 Year(s) 至 7.00 Year(s)(—)
性别
All

入选标准

  • ASA 1 and 2 Scheduled for elective abdominal, inguinal, hip and femur surgeries.

排除标准

  • History of allergy to local anesthetics Coagulopathic disorders Cardiac or Renal diseases Infection at site of injection.

结局指标

主要结局

Duration of analgesia

时间窗: postoperatively at 10min, 20min , 2 hour, 6hrs, 12hrs and 24 hrs.

次要结局

  • a)To assess frequency of rescue analgesics(b)To assess the total doses of rescue analgesics)

研究者

发起方
St Johns Medical College and Hospital
申办方类型
Private medical college

研究点 (1)

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