Intravenous Fluid for Pediatric Migraine in the Emergency Department (EDMigraine3)

This study is currently recruiting participants.
Verified May 2012 by University of Alberta
Sponsor:
Information provided by (Responsible Party):
Lawrence Richer, University of Alberta
ClinicalTrials.gov Identifier:
NCT01073787
First received: February 22, 2010
Last updated: May 2, 2012
Last verified: May 2012

February 22, 2010
May 2, 2012
March 2010
July 2012   (final data collection date for primary outcome measure)
Headache pain [ Time Frame: 30 minutes ] [ Designated as safety issue: Yes ]
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)
Same as current
Complete list of historical versions of study NCT01073787 on ClinicalTrials.gov Archive Site
  • Nausea [ Time Frame: 30 minutes ] [ Designated as safety issue: Yes ]
    Severity will be assessed using: (1) Visual Analogue Scale; (2) Four categories (none, mild, moderate, severe)
  • Vomiting [ Time Frame: 30 minutes ] [ Designated as safety issue: No ]
  • Use of rescue medication [ Time Frame: 24 hours ] [ Designated as safety issue: No ]
    Use of any rescue medication after leaving the Emergency Department
  • Headache recurrence [ Time Frame: 24 hours ] [ Designated as safety issue: No ]
    Recurrence or worsening of headache after leaving the Emergency Department
  • Return to Emergency Department [ Time Frame: 24 hours ] [ Designated as safety issue: No ]
    Return to Emergency Department for treatment of migraine within 24 hours
Same as current
Not Provided
Not Provided
 
Intravenous Fluid for Pediatric Migraine in the Emergency Department
Single-blind, Placebo-challenge Study of Intravenous Fluid Hydration in the Management of Pediatric Migraine in the Emergency Department

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.

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.

Interventional
Phase 1
Phase 2
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Subject)
Primary Purpose: Treatment
  • Migraine
  • Headache
Drug: Normal saline
10 ml/kg of normal saline will be administered over 30 minutes
Other Name: 0.9% sodium chloride and water
  • Active Comparator: Normal saline
    Intervention: Drug: Normal saline
  • Experimental: Normal saline and possible medication
    Intervention: Drug: Normal saline
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
60
July 2012
July 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • 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

Exclusion Criteria:

  • 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
Both
5 Years to 17 Years
No
Contact: Lawrence P Richer, MD, MSc 780-407-7329 lricher@ualberta.ca
Contact: William Craig, MD, MSc 780-407-3555 William.Craig@albertahealthservices.ca
Canada
 
NCT01073787
Pro00008034
No
Lawrence Richer, University of Alberta
University of Alberta
Not Provided
Principal Investigator: Lawrence P Richer, MD, MSc University of Alberta
University of Alberta
May 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP