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临床试验/NCT07602894
NCT07602894招募中不适用

Efficacy of Ultrasound-guided Sacral Multifidus Plane Block as Perioperative Analgesia for Anal and Penile Surgeries in High-risk Pediatric Patients

Zagazig University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年7月20日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
60
试验地点
1

研究概览

简要总结

Perioperative pain management in pediatric patients, especially for anorectal and penile surgeries, presents significant challenges for anesthetists. Complications associated with systemic analgesia, such as respiratory issues, cardiovascular problems, and neurological effects, can be avoided by using regional anesthesia. This study aims to evaluate the effectiveness of Ultrasound-Guided Sacral Multifidus Plane Block as a method for perioperative analgesia in high-risk pediatric patients undergoing anorectal and penile surgeries, to reduce the risks associated with systemic analgesia.

详细描述

Effective postoperative pain control in pediatric patients remains a major concern, particularly in those undergoing anal, perineal and penile surgeries. Inadequate analgesia is associated with delayed recovery, increased stress response, prolonged hospitalisation, and higher postoperative morbidity. This study aims to evaluate the efficacy of ultrasound-guided sacral multifidus plane block as a method for perioperative analgesia in high-risk pediatric patients undergoing anorectal and penile surgeries, to reduce the risks associated with systemic analgesia. This involves the administration of local anesthetics in the plane between the sacral multifidus muscle and the intermediate sacral crest bilaterally.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
12 Months 至 12 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Parents or caregivers' acceptance.
  • High-risk pediatric patients (the American Society of Anesthesiologists physical status class III-IV)
  • Body mass index equal to 5%: 85% of the same age and sex.

排除标准

  • Child with a contraindication to the regional block, such as infection at the site of injection, or coagulopathy.
  • Pre-existing neurological disorders.

研究者

申办方类型
Other Gov
责任方
Sponsor

研究点 (1)

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