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临床试验/IRCT2012102311228N1
IRCT2012102311228N1已完成未知

Comparison of preoperative percutaneous electrical nerve stimulation on intensity of pain surgery in patient under inguinal herniorrhaphy in case and control groups

Vice Chancellor for research, Kashan University of Medical Sciences0 个研究点目标入组 66 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
66

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
20 years 至 50 years(—)
性别
Male

入选标准

  • Male, aged 20 to 50, suffering from inguinal hernia; Use of Liechtenstein surgical procedure; Surgery performed in the morning to avoid circadian cycle; Physical status of ASA I or II; Absence of hearing, visual or talking impairment; Lack of cognitive impairment; No exclusion criteria
  • Exclusion criteria: Conditions prohibiting the use of TENS, (such as pacemakers, because of the unknown effects of TENS on electrical conduction system or placing the electrode directly on open wounds); Obesity (weight more than 100 pounds above ideal weight); Recurrent, incarcerated and bilateral hernia; Skin infection or severe skin disease in the place of the electrodes; Chronic use of narcotics or antidepressant drugs

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for research, Kashan University of Medical Sciences

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