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临床试验/NCT00257010
NCT00257010已完成3 期

Long-Term, Open-Label Safety Study of Oral Almotriptan Malate 12.5 mg in the Treatment of Migraine in Adolescents

Janssen-Ortho LLC0 个研究点目标入组 447 人开始时间: 2005年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
447
主要终点
Number of Pain Free Headaches at 2 and 24 Hours Post-Dose

研究概览

简要总结

The purpose of this study is to evaluate the long-term safety of almotriptan malate (a migraine headache medication) in the treatment of migraine headaches in adolescents for up to one year.

详细描述

Almotriptan malate, and several other treatments for migraine headaches, known as triptans, are approved for the treatment of migraine headaches in adults. To date, none of these have been approved by the Food and Drug Administration (FDA) for use in adolescents. This is an open-label, multi-center study that will enroll approximately 450 patients aged 12 - 17 years old with a history of one to 14 migraines per month for the 6 months prior to entering the study. The total study duration will be up to one year. There is a screening phase to determine if the patient is eligible for study entry, followed by an open-label treatment phase that can last up to one year. Almotriptan malate 12.5 mg tablets will be used to treat all migraine headaches during the study, as needed. The primary outcome of the study is an assessment of the long-term safety of almotriptan malate in adolescent migraine sufferers. The study hypothesis is that the almotriptan malate will be safe and well tolerated in the treatment of adolescent migraine headaches. Safety measurements will be performed at set time points during the study and will include laboratory tests, physical and neurological exams, electrocardiograms (ECGs) and the incidence of adverse events. A diary will be completed by the patient for each migraine headache for which they take almotriptan malate. Migraine pain information and almotriptan malate use will be recorded in the headache diary. An equal number of patients in the 12 - 14 year old range as the 15 - 17 year old range will be enrolled. Patients will take one 12.5 mg almotriptan malate tablet by mouth after the onset of migraine headache pain. The dose may be repeated once if the pain continues 2 hours after the first dose, but no more than 2 doses can be taken within a 24-hour period. Study medication will be taken for up to one year.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
12 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Have a history of migraine for at least one year
  • Have an average of 1 - 14 migraines per month for the 6 months prior to study entry
  • Able to swallow oral medication
  • Able to complete a headache diary
  • Only taking one migraine preventive medication and on the same dose of that medication for at least 30 days before entering the study)

排除标准

  • Have an allergy to almotriptan malate or have stopped taking almotriptan malate due to side effects
  • Have 15 or more days within a month in which you have a headache
  • Usually experience migraine aura (most common symptoms being visual disturbances or tingling sensations before migraine pain begins) without a headache
  • Experience more than 6 non-migraine headaches per month

研究组 & 干预措施

Almotriptan Malate

Experimental

Patients will take one 12.5 mg almotriptan malate tablet by mouth after the onset of migraine headache pain

干预措施: Almotriptan Malate (Drug)

结局指标

主要结局

Number of Pain Free Headaches at 2 and 24 Hours Post-Dose

时间窗: 2 hours and 24 hours post-dose

Headache pain free is defined as a decrease in baseline pain intensity from severe, moderate or mild to no pain, without the use of supplemental pain medication and/or anti-emetic medication (including a second dose of study medication) within 2 (or 24) hours of first dose of study medication. Sustained pain free is defined as pain free at 2 and 24 hours without the use of supplemental pain medication and/or anti-emetic medication (including a second dose of study medication) within 24 hours.

次要结局

  • Number of Headaches Achieving Pain Relief at 2 and 24 Hours Post-Dose(2 hours and 24 hours post-dose)
  • Number of Headaches With Phonophobia(Baseline (after onset of migraine headache pain and before treatment), 2 hours and 24 hours post-dose)
  • Number of Headaches With Nausea(Baseline (after onset of migraine headache pain and before treatment), 2 hours and 24 hours post-dose)
  • Number of Headaches With Vomiting(Baseline (after onset of migraine headache pain and before treatment), 2 hours and 24 hours post-dose)
  • Number of Headaches With Photophobia(Baseline (after onset of migraine headache pain and before treatment), 2 hours and 24 hours post-dose)

研究者

申办方类型
Industry
责任方
Sponsor

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