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临床试验/EUCTR2018-001261-16-SE
EUCTR2018-001261-16-SE进行中(未招募)1 期

Betamethasone (Betapred®) as premedication for reducing postoperative vomiting and pain after tonsillectomy – a randomized, double-blind, placebo-controlled trial

ÖNH-kliniken Sunderby Sjukhus0 个研究点目标入组 100 人开始时间: 2018年4月18日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1.Signed informed consent
  • 2.Age over 12 years
  • 3.Planned for elective bilateral tonsillectomy
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 50
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 50
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 1

排除标准

  • 1.Insulin dependent diabetes mellitus
  • 2.NSAID or corticosteroid intolerance
  • 3.Pregnancy
  • 4.Gastric ulcer
  • 5. Immunodeficiency
  • 6. Treatment for chronic pain
  • 7. Psychiatric disorders

研究者

发起方
ÖNH-kliniken Sunderby Sjukhus

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