跳至主要内容
临床试验/EUCTR2018-002224-17-NL
EUCTR2018-002224-17-NL进行中(未招募)1 期

GON-injection for a sooner and better treatment of cluster headache: a double-blind randomized controlled trial - CHIANTI

eids Universitair Medisch Centrum0 个研究点目标入组 80 人开始时间: 2018年12月20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)
入组人数
80

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

入选标准

  • - Patients have to be diagnosed with episodic cluster headache according to the international classification of headache disorders – third edition beta, ICHD-3b
  • - Patients have to be aged 18-65 years
  • - Patients need to be newly diagnosed and treatment naïve, or already diagnosed and currently free from prophylactic treatment
  • - Patients need to have a mean of more than 1 attack per day in the 3 days preceding inclusion.
  • - Patients should be in their cluster period for shorter than 4 weeks before inclusion.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 80
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - A contraindication for treatment with steroids or verapamil
  • - The use of anticoagulants or known bleeding disorder.
  • - Use of any prophylactic medication for cluster headache
  • - Patients with a history of other primary headache who are currently using prophylactic medication for this headache
  • - Pregnancy

研究者

相似试验