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临床试验/NCT03056352
NCT03056352已完成1 期

Metoclopramide for Post-Traumatic Headache. A Pilot Study

Montefiore Medical Center1 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2017年3月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
21
试验地点
1
主要终点
Number of Participants With Sustained Headache Relief

研究概览

简要总结

Post-traumatic headache is common. We are determining short and longer-term outcomes among patients treated for post-traumatic headache with IV metoclopramide.

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
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Traumatic injury to the head has occurred
  • Headache has developed within 7 days of injury to the head
  • Headache is not better accounted for by another diagnosis (eg, previous history of migraine or tension-type headache)
  • The headache must be rated as moderate or severe in intensity at the time of initial evaluation.
  • The plan of the attending emergency physician must include treatment with parenteral metoclopramide.

排除标准

  • Patients will be excluded if more than ten days have elapsed since the head trauma, if the headache has already been treated with an anti-dopaminergic medication, or for medication contra-indications including pheochromocytoma, seizure disorder, Parkinson's disease, use of monoamine oxidase inhibitors, and use of anti-rejection transplant medications. Patients will not be excluded for pregnancy or breast-feeding.

研究组 & 干预措施

Metoclopramide

Experimental

Metoclopramide 20mg + diphenhydramine 25mg administered intravenously over 15 minutes

干预措施: Diphenhydramine (Drug)

Metoclopramide

Experimental

Metoclopramide 20mg + diphenhydramine 25mg administered intravenously over 15 minutes

干预措施: Metoclopramide (Drug)

结局指标

主要结局

Number of Participants With Sustained Headache Relief

时间窗: 2 hours thru 48 hours after treatment

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 medication administration.

次要结局

  • Number of Participants Satisfied With Medication; Assessed by Self-evaluation(48 hours after treatment)
  • Post Concussion Symptoms Assessed by Post-concussive Symptom Scale(7 days)

研究者

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

Benjamin W. Friedman, MD

Professor

Montefiore Medical Center

研究点 (1)

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