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临床试验/IRCT2016022026217N2
IRCT2016022026217N2已完成2 期

The effect and comparison of oral and intravenous Acetaminophen in pain control and Consumption opioid in post cardiac surgery patients

Vice Chancellor for research, Lorestan University of Medical Science0 个研究点目标入组 160 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
160

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
18 years 至 65 years(—)
性别
All

入选标准

  • all patients who underwent CABG surgery with or without valve replacement; age older than 18 or less than 65 years; absence of addiction to drugs or alcohol; absence of allergy or hypersensitivity to acetaminophen or narcotics; absence of impaired kidney function (creatinine level Less than 2 milligrams per deciliter); no history of liver failure; no history of sleep apnea. Exclusion criteria: Visual analog scale score is higher than 7 after extubation; not wanting to continue cooperation?; use of narcotic drugs and sedatives during the procedure?; decreased level of consciousness of the patient during the study.

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for research, Lorestan University of Medical Science

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