跳至主要内容
临床试验/CTRI/2018/01/011445
CTRI/2018/01/011445尚未招募不适用

Comparison of analgesic efficacy of ultrasound guided quadratus lumborum block versus transversus abdominis plane block for pyeloplasty for children- a randomized, double blind, controlled trial.

AIIMS New Delhi1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2018年1月2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
40
试验地点
1
主要终点
Secondary Objectives

研究概览

简要总结

Renal  surgeries  are commonly performed procedures in children and are associated with significant post-operative pain.Effective postoperative analgesia is essential to allow coughing, early mobilization, and to reduce the incidence of post-operative respiratory complications. Compared to systemic opioids , neuraxial analgesia  and  peripheral  nerve blockade  techniques  can  provide superior analgesia while avoiding majority of side effects of opioids as well as  NSAIDs.

The transversus abdominis plane (TAP) block and quadratus lumborum(QL) block are the truncal nerve blocks that targets the lower thoracic and upper lumbar nerves as they course through the inter-fascial planes and provides analgesia for procedures involving the abdominal wall.

Quadratus lumborum (QL) block  is a newly introduced variation of TAP block, reported to provide excellent post-operative analgesia in; pediatric patients undergoing radical nephrectomy (2), colostomy closure (3), pyeloplasty .

研究设计

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

入排标准

年龄范围
2.00 Year(s) 至 10.00 Year(s)(—)
性别
All

入选标准

  • American Society of Anaesthesiology physical status I and II Posted for elective pyeloplasty.

排除标准

  • Refusal of parents or guardians to participate in the study
  • Developmental delay and mental retardation
  • History of sensitivity to drugs used in the study
  • Coagulopathy
  • Infection at the puncture site
  • Significant cardiac renal or liver disease.

结局指标

主要结局

Secondary Objectives

时间窗: at 1, 2, 4, 6, 8, 12, 18, 24 hours

To compare the intraoperative and post operative analgesic consumptions and post operative VAS scores

时间窗: at 1, 2, 4, 6, 8, 12, 18, 24 hours

Primary outcome

时间窗: at 1, 2, 4, 6, 8, 12, 18, 24 hours

To compare the incidence of nausea or vomiting, excessive sedation and respiratory depression

时间窗: at 1, 2, 4, 6, 8, 12, 18, 24 hours

次要结局

  • Secondary Objectives(To compare the incidence of nausea or vomiting, excessive sedation and respiratory depression)

研究者

发起方
AIIMS New Delhi
申办方类型
Research institution and hospital

研究点 (1)

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