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临床试验/CTRI/2023/08/057050
CTRI/2023/08/057050尚未招募2 期

Comparison of two different dosage of dexmeditomidine with bupivacaine in paediatric caudal Anaesthesia for infraumbilical surgeries

Jawaharlal Nehru Medical College1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年9月30日最近更新:

试验速览

阶段
2 期
状态
尚未招募
入组人数
60
试验地点
1
主要终点
Caudal dexmeditomidine (1mcg/kg) with 0.25% bupivacaine for paediatric infra umbilical surgeries achieved significant post operative pain relief compared to caudal dexmeditomidine (0.5mcg/kg) with 0.25% bupivacaine.

研究概览

简要总结

Caudal epidural block is one of the most common regional techniques in paediatric anesthesia .Caudal block is a safe and reliable technique, easy to perform and has been foundto be very effective in children,we will conduct this study to compare two different dosages, 1μg/kg dexmedetomidine with bupivacaine during caudal epidural block which has been proved to increase analgesia duration in comparison with 0.5μg/kg dexmedetomidine as an adjuvant for duration of postoperative analgesia ,hemodynamic changes and adverse effects.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant Blinded

入排标准

年龄范围
6.00 Month(s) 至 6.00 Year(s)(—)
性别
All

入选标准

  • Age group of 6 months to 6 years ASA Class I & II patients.
  • Children posted for infraumbilical surgeries.

排除标准

  • ASA grade 3, 4 and
  • allergy to any of the study drug Cardiac, Respiratory diseases Hepatic, Renal dysfunction developmental delay or mental retardation Infection at the site of caudal block.

结局指标

主要结局

Caudal dexmeditomidine (1mcg/kg) with 0.25% bupivacaine for paediatric infra umbilical surgeries achieved significant post operative pain relief compared to caudal dexmeditomidine (0.5mcg/kg) with 0.25% bupivacaine.

时间窗: 240 minutes

次要结局

  • Incidence of side effects was less in 0.5 mcg/kg dexmeditomidine group when compared to 1mcg/kg group(240 minutes)

研究者

申办方类型
Private medical college

研究点 (1)

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