跳至主要内容
临床试验/NCT01073787
NCT01073787已完成1 期

Single-blind, Placebo-challenge Study of Intravenous Fluid Hydration in the Management of Pediatric Migraine in the Emergency Department

University of Alberta1 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2010年7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
46
试验地点
1
主要终点
Headache pain

研究概览

简要总结

The purpose of this study is to evaluate the effect of intravenous fluid (0.9% sodium chloride and water) alone on headache pain in children with migraine visiting the Emergency Department.

详细描述

Migraine is a common and disabling disorder for children. The pain may be severe and relatively few effective medications are approved for use in children. The Emergency Department (ED) remains an important resource for children suffering from migraine whom have not responded to their usual therapy. While a number of effective intravenous therapies have been studied in adults, there has been only one such study in children. As such, emergency physicians have little or no information about the safety and efficacy of these medications in children. However, the conduct of clinical trials where pain is the outcome measure is often limited by a high placebo-response rate. The expectation of treatment can significantly alter the response to medications especially when pain severity is the outcome measure. Moreover, the investigators have found that intravenous fluid alone may help to treat migraine headache in children. The investigators propose a study to examine the response to intravenous fluid hydration as initial therapy comparing a group with expectation of medication and another group without the initial expectation of medication. The results of the study will help to estimate the rate of response to intravenous fluid and to evaluate the placebo-effect (i.e. expectation of treatment) in studies of migraine treatment in the ED. Exposure to additional and possibly unnecessary medications will thus be minimized and the results of future trials more definitive on the effect of the study medication.

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
Single (Participant)

入排标准

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

入选标准

  • •Diagnosis of migraine or probable migraine (with or without aura) per the International Classification of Headache Disorders (2nd edition)
  • •Visiting the Emergency Department for migraine treatment
  • •Emergency Department physician has chosen to administer intravenous medication
  • •Has taken usual therapy at home or at least one does of either ibuprofen or acetaminophen in the Emergency Department

排除标准

  • •Other probable cause for headache (e.g. ventriculoperitoneal shunt, neoplasm, intracranial cyst)
  • •Head trauma causing loss of consciousness within 1 week of presentation
  • •Fever (temperature > 38.5 oC)
  • •Signs or symptoms of meningitis

研究组 & 干预措施

Normal saline

Active Comparator

干预措施: Normal saline (Drug)

Normal saline and possible medication

Experimental

干预措施: Normal saline (Drug)

结局指标

主要结局

Headache pain

时间窗: 30 minutes

Pain will be assessed using three measures: (1) Nine Faces Pain scale; (2) Visual Analogue Scale; and (3) Four categories (none, mild, moderate, or severe)

次要结局

  • Headache recurrence(24 hours)
  • Nausea(30 minutes)
  • Use of rescue medication(24 hours)
  • Return to Emergency Department(24 hours)
  • Vomiting(30 minutes)

研究者

申办方类型
Other
责任方
Sponsor
主要研究者

Lawrence Richer

Principal Investigator

University of Alberta

研究点 (1)

Loading locations...

相似试验