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临床试验/IRCT201106146256N2
IRCT201106146256N2已完成2 期

The comparison between effect of oral propranolol, lorazpam and propranolol-lorazpam in reduction of preoperative anexiety

vice-chancellor for research of Qazvin universityof medical science0 个研究点目标入组 75 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
75

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 45 years(—)
性别
All

入选标准

  • Grasp testimonial; elective minor to moderate surgery as: inguinal hernia, trans urethral lithothomy , colles fx, tibia fx; age 18-45 and ASA class Iand II
  • Exclusion criteria:
  • History of chronic consumption of bzd antipsychotics, opium and amphetamines; history of panic attack or any psychologic disorder; history of CHF, asthma COPD ,dm type Iand II; history of hypertension; history of any anti hypertension drug consumption and history of any food and drugs allergy

排除标准

  • 未提供

研究者

发起方
vice-chancellor for research of Qazvin universityof medical science

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