跳至主要内容
临床试验/EUCTR2006-004257-14-DK
EUCTR2006-004257-14-DK进行中(未招募)1 期

A Multicenter, Double-Blind, Placebo and Active-Controlled, Parallel Group Study to Compare the Efficacy and Safety of Oral MK-0974 With Placebo and Zolmitriptan for the Acute Treatment of Migraine With or Without Aura - MK-0974 Pivotal Study 1 - worldwide (with active comparator)

Merck & Co., Inc.0 个研究点目标入组 1,800 人开始时间: 2006年12月12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
1,800

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

  • Patient has at least 1 year history of migraine (with or without aura).
  • Females of child bearing potential must use acceptable contraception throughout trial.
  • Patient is in general good health based on screening assessment.
  • 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
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Patient is pregnant/breast-feeding (or is a female expecting to conceive during study period).
  • Patient has uncontrolled hypertension (high blood pressure), uncontrolled diabetes, HIV disease, or other significant disease.
  • Patient has major depression, other pain syndromes that might interfere with study assessments, psychiatric conditions, dementia, or significant neurological disorders (other than migraine).
  • Patient has a history of gastric, or small intestinal surgery, or has a disease that causes malabsorption.
  • Patient has a history of cancer within the last 5 years.
  • Patient has history or presence of a significant cardiovascular disorder (e.g. acute
  • coronary syndrome [e.g. MI or unstable angina]; coronary artery intervention [e.g.
  • CABG or PTCA]; congestive heart failure or arrhythmia.
  • Note: Patients with evidence of an MI on ECG will be excluded.

研究者

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