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临床试验/EUCTR2018-004875-11-IT
EUCTR2018-004875-11-IT进行中(未招募)1 期

A RandomizEd, double-blind, cross-over Study to assess Erenumab effecT on BRAIN networks function and structure in comparison to placebo in episodic migraine patients (RESET BRAIN) - RESET BRAI

OVARTIS FARMA S.P.A.0 个研究点目标入组 140 人开始时间: 2021年1月7日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
140

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) Adult patients, aged between 18 and 65 years
  • 2) Provided informed consent
  • 3) History of migraine with or without aura for at least 12 months prior to screening according to IHS classification ICHD-3, based on medical records and/or patient self-report
  • 4) Migraine frequency: = 4 and < 15 migraine days per month on average across the 3 months prior to screening and confirmed during the baseline phase based on diary evaluation
  • 5) Headache frequency: <15 headache days per month on average across the 3 months prior to screening and confirmed during the baseline phase based on diary calculation
  • 6) Failure to 2 or more previous prophylactic treatment categories locally indicated for migraine
  • 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 137
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 3

排除标准

  • 1) Older than 50 years of age at migraine onset.
  • 2) History of cluster headache or hemiplegic migraine headache.
  • 3) History of head trauma or seizure or major psychiatric disorders.
  • 4) Currently receiving (or have received less than 60 days or 5 half-lives prior to the start of the baseline period, during the baseline period, or treatment period) any other prophylactic treatment for migraine and/or prohibited medications, non-pharmacologic interventions or devices (any substance, non-pharmacologic intervention or device acting at central nervous system).
  • 5) Pregnant or breastfeeding.
  • 6) All the clinical conditions for which undergoing an MRI scan is contraindicated.

研究者

发起方
OVARTIS FARMA S.P.A.

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