Value of Intravenous Fluids in the Emergent Treatment of Pediatric Migraine

Status: Recruiting
Location: See location...
Intervention Type: Drug, Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to compare intravenous (IV) fluids in pediatric patients with migraine. The main questions it aims to answer are: * Does a large amount of fluids (bolus) improve pain * Does a large amount of fluids (bolus) reduce admissions to the hospital for migraine Participants will be asked to report their pain and have vital signs checked every 30 minutes for two hours. Researchers will compare a large amount of fluids (bolus) to a small amount (half maintenance) to see if there is a difference in pain improvement.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 5
Maximum Age: 21
Healthy Volunteers: t
View:

• At least 1 prior headache

• Minimum pain score of 10mm

• Headache lasting 2-72 hours

• At least two of the following four: 1 Bifrontal/bitemporal or unilateral location, 2 Pulsating quality, 3 Moderate or severe pain intensity, 4 Aggravation by or causing avoidance of routine physical activity

• At least one of the following: 1 Nausea and/or vomiting, 2Photophobia and phonophobia, 3 Not better accounted for by another ICHD-3 diagnosis

Locations
United States
Ohio
Dayton Children's Hosptial
RECRUITING
Dayton
Contact Information
Primary
Jonathan Elliott, MD
elliottj1@childrensdayton.org
(812) 582-3059
Time Frame
Start Date: 2023-06-27
Estimated Completion Date: 2025-06
Participants
Target number of participants: 134
Treatments
Experimental: Bolus
Will receive a normal saline bolus
Placebo_comparator: Control
Will receive 1/2 maintenance normal saline
Related Therapeutic Areas
Sponsors
Leads: Dayton Children's Hospital

This content was sourced from clinicaltrials.gov