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临床试验/IRCT20220110053685N1
IRCT20220110053685N1
招募中
3 期

Therapeutic effect of 0.5% thymolol eye drops on rosacea lesions of the face in comparison with placebo

Tehran University of Medical Sciences0 个研究点目标入组 44 人开始时间: 待定最近更新:

概览

阶段
3 期
状态
招募中
入组人数
44

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

  • Ability to cooperate to refer at the appointed time.
  • Ability to cooperate to necessary cooperation in taking the drug.
  • consciously understanding the consent and accepting its provisions.
  • agreeing not to breastfeed and pregnancy during the study and one month later in women of childbearing age.
  • willingness not to take other drugs during the study.
  • Have the criteria for diagnosing rosacea.

排除标准

  • Receive any research medication within 30 days prior to enrollment.
  • history of allergy to beta\-blocker,
  • pregnancy or attempt to conceive or breastfeed.
  • severe depression.
  • history of hypotension or bradycardia,
  • history of myocardial infarction or heart failure.
  • history of arrhythmia,
  • history of asthma or bronchospasm.
  • Taking any rosacea stimulant such as calcium channel blocker during the study.
  • taking alpha or beta blocker drugs.

研究者

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