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临床试验/PACTR201505001103180
PACTR201505001103180招募中未知

Sixty patients of both sexes between 2 and 10 years old, ASA I ¿ II physical status, undergoing midline abdominal procedures are involved in this randomized controlled trial. Patients were randomly allocated into one of two groups (thirty patients each) ; group R (RSB group) and group C (control group). Both groups received general anesthesia . Group R received bilateral rectus sheath block with 0

Ain Shams university0 个研究点目标入组 70 人开始时间: 2015年4月16日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
入组人数
70

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
2 Year(s) 至 10 Year(s)(—)
性别
All

入选标准

  • both sexes, ASA I ¿ II physical status, scheduled for elective abdominal midline operation.

排除标准

  • Patients with hepatic disease, bleeding or neurological disorders, known hypersensitivity to local anesthetics, evidence of peritonitis, sepsis, or infection at the site of needle insertion and those who require emergency operations were excluded from the study.

研究者

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