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临床试验/NCT01825941
NCT01825941已完成4 期

Diphenhydramine as Adjuvant Therapy for Acute Migraine. A Randomized Trial.

Montefiore Medical Center1 个研究点 分布在 1 个国家目标入组 208 人开始时间: 2013年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
208
试验地点
1
主要终点
Number of Participants With Sustained Headache Relief Assessed by Self-evaluation

研究概览

简要总结

Parenteral diphenhydramine is commonly used as adjuvant therapy for acute migraine despite the fact that data supporting this practice do not exist. The investigators propose a randomized double blind study to test the hypothesis that 50mg of intravenous diphenhydramine, when added to standard migraine therapy, will result in a greater rate of sustained headache relief than standard migraine therapy alone. For this study, standard migraine therapy will be 10mg of intravenous metoclopramide. Sustained headache relief is defined as achieving a headache level of "mild" or "none" within two hours and maintaining a level of "mild" or "none" for 48 hours. Patients who present to the Montefiore emergency room (Bronx, NY) with an acute migraine will be approached for participation. They will be screened for medication contra-indications and non-migraine etiologies of headache. The study will be randomized. Assignment will be concealed. Participants and researchers will be blinded. Efficacy outcomes and adverse events will be assessed every half hour for two hours in the Emergency Department and by telephone 48 hours after medication administration. A sample size calculation, based on pilot data, revealed the need for 374 participants. An interim analysis will be performed after 200 participants have been enrolled with the goal of assessing for lack of conditional power.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
21 Years 至 64 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Acute migraine headache
  • Present to our emergency room in the Bronx, NY for treatment of migraine headache

排除标准

  • Temperature > 100.3 F
  • Pheochromocytoma
  • Seizure disorder
  • Parkinson's disease
  • Use of monoamine oxidase (MAO) inhibitors
  • Use of anti-rejection transplant medications
  • Use of potassium supplements
  • Use of pramlintide

研究组 & 干预措施

Metoclopramide + Diphenhydramine

Active Comparator

Metoclopramide 10 milligrams + Diphenhydramine 50 milligrams, administered as an intravenous drip over 15 minutes

干预措施: metoclopramide (Drug)

Metoclopramide + Diphenhydramine

Active Comparator

Metoclopramide 10 milligrams + Diphenhydramine 50 milligrams, administered as an intravenous drip over 15 minutes

干预措施: diphenhydramine (Drug)

Metoclopramide + placebo

Placebo Comparator

Metoclopramide 10mg + placebo, administered intravenously over 15 minutes

干预措施: metoclopramide (Drug)

Metoclopramide + placebo

Placebo Comparator

Metoclopramide 10mg + placebo, administered intravenously over 15 minutes

干预措施: placebo (Drug)

结局指标

主要结局

Number of Participants With Sustained Headache Relief Assessed by Self-evaluation

时间窗: up to 2 hours in Emergency Department, 48 hours after discharge from Emergency Department

Sustained headache relief is defined as achieving a headache level of "mild" or "none" within two hours and maintaining a level of "mild" or "none" for 48 hours. Patient self-evaluated pain level is solicited every half hour for two hours in the Emergency Department and then by telephone 48 hours after discharge from emergency department

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Benjamin W. Friedman, MD

Associate professor of Emergency Medicine

Montefiore Medical Center

研究点 (1)

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