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临床试验/NCT02664116
NCT02664116Unknown4 期

IM Ketorolac vs Diclofenac Potassium Powder for Oral Solution (Cambia) for the Acute Treatment of Severe Migraine

Scripps Health1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2016年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
入组人数
40
试验地点
1
主要终点
Pain relief, 0-3 scale

研究概览

简要总结

This research will be conducted to see if the oral drug Cambia is as effective in relieving severe migraine headaches as the injectable drug ketorolac.

详细描述

The treatment of severe migraine often requires a patient office visit or treatment in the ER or urgent care setting. This is due to the minimal efficacy of PO treatments once migraine is severe, and therefore the need for parenteral treatments. IM Ketorolac is one mainstay of parenteral treatment. There is an unmet need for effective at-home treatment regimens for severe migraine. Despite FDA approval of Cambia for acute migraine treatment, insurance is reticent to cover the treatment due to higher cost in comparison to generic diclofenac tablets, despite superior efficacy of Cambia in comparison to generic diclofenac tablets (Diener, Cephalalgia 2006). One objective of this study would be to provide rationale to justify the insurance coverage of this treatment in comparison to generic tablets, because at home treatment is less costly than office visit or emergency department visit to receive IM ketorolac.

A previous study of Cambia demonstrated that this formulation of diclofenac potassium for oral solution is effective in reducing pain intensity within 30 minutes, which may be related to the 15-minute Tmax associated with this formulation. The rapid-onset benefits were sustained through 24 hours post-treatment (Lipton, Cephalalgia 2010)

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
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients who meet IHS criteria for migraine
  • Age 18 to 65
  • At least 2 migraine attacks per month
  • Able to give written consent
  • Willing to complete the entire course of the study
  • Current headache duration greater than or equal to 36 hours

排除标准

  • Pregnant or nursing
  • Significant medical or psychiatric disease
  • History of gastritis, gastric ulcer, GI bleed
  • Renal insufficiency
  • Hepatic insufficiency
  • History of opioid dependence within the last 10 years or currently
  • Any current or prior use of DICLOFENAC POTASSIUM POWDER FOR ORAL SOLUTION (CAMBIA)
  • Past allergic reaction to DICLOFENAC or other NSAIDs

研究组 & 干预措施

Cambia

Experimental

Diclofenac postassium powder for oral solution and placebo injection

干预措施: Diclofenac postassium powder for oral solution and placebo injection (Drug)

ketorolac

Active Comparator

ketorolac intramuscular injection and placebo oral solution

干预措施: Ketorolac intramuscular injection and placebo oral solution (Drug)

结局指标

主要结局

Pain relief, 0-3 scale

时间窗: Change from baseline pain rating at 5, 10, 15, 30, and 60 minutes post intervention

Pain free response, 0-3 scale

时间窗: 2 hours post intervention

Sustained pain free response, 0-3 scale

时间窗: 24 hours post intervention

次要结局

  • Change in severity of migraine associated symptoms(5, 10, 15, 30, 60, 120 minutes and 24 hours post intervention)
  • Return to function(24 hours post intervention)

研究者

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

Emily Rubenstein Engel

Associate Director, Dalessio Headache Center, Scripps Clinic

Scripps Health

研究点 (1)

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