Nitrous Oxide for Acute Migraine Pain in the Emergency Room (ED)

NACompletedINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

June 30, 2011

Primary Completion Date

August 31, 2014

Study Completion Date

January 31, 2015

Conditions
MigrainePain
Interventions
DRUG

Nitrous Oxide

Once consent is obtained, the research assistant will notify the charge RN and MD of the patient's study participation. The patient will then be placed in a treatment room and nitrous oxide will be administered per the existing protocol. Each participant will be given nitrous oxide until he/she reports a pain score of zero or up to fifteen minutes. Study subjects will be asked to rate their pain on a scale of 0-10 before the treatment and after the treatment, the time duration of administering nitrous oxide will be recorded. In addition, the pain scores at 30, 60, 90, and 120 minutes post baseline measurement will be collected in order to evaluate the sustained effect of nitrous oxide in treating acute migraine pain. Someone from the study will also make a follow-up phone call 24 - 48 hours to see if pain relief persisted.

Trial Locations (1)

Unknown

Children's Hospitals and Clinics of Minnesota, Minneapolis

All Listed Sponsors
lead

Children's Hospitals and Clinics of Minnesota

OTHER

NCT01287052 - Nitrous Oxide for Acute Migraine Pain in the Emergency Room (ED) | Biotech Hunter | Biotech Hunter