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NMDA Receptor Antagonist

Intravenous ketamine for Migraine

Phase 4
Waitlist Available
Research Sponsored by The Brooklyn Hospital Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up throughout study period (105 mins)
Awards & highlights

Study Summary

The hypothesis of the study is that sub-dissociative dose ketamine will prove to be superior to or as standard therapy, ketorolac, in the treatment of acute tension type headache (TTH) as measured by the 10 point Numerical Rating Scale (NRS. The aim of the study is to compare the safety & efficacy of intravenous sub-dissociative dose ketamine versus ketorolac for acute treatment of migraines in the Emergency Department (ED) The primary endpoints are: Patient perception of pain as described by the use the Numerical Rating Scale (NRS) at 30 minutes. The secondary endpoints are: Frequency and mean dose of rescue/additional doses of therapy at 15, 30, 45, 60, 75, 90 min, Number of emergency department re-visits for acute migraine one month post discharge, incidence of dissociative effects (characterized by hallucination, disorientation, confusion, agitation, delirium, dreams) during study period, incidence of nausea, vomiting, or worsening headache, Incidence of bad taste, Incidence of burning sensations in the nostrils, incidence of hypertension, time to patient discharge from the initiation of study medication/placebo, patient satisfaction of pain control based on a Likert Scale.

Eligible Conditions
  • Migraine

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~throughout study period (105 mins)
This trial's timeline: 3 weeks for screening, Varies for treatment, and throughout study period (105 mins) for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Pain scores
Secondary outcome measures
Incidence of adverse events
length of stay
mean dose of rescue analgesia required

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Intravenous ketamineExperimental Treatment2 Interventions
Arm will include 0.3 mg/kg intravenous piggyback ketamine over 10 minutes for 1 dose and a 1ml normal saline placebo via intravenous push
Group II: ketorolacActive Control2 Interventions
Arm will include 30mg ketorolac intravenous push and 50ml normal saline over 10 minutes
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Ketamine
FDA approved
Normal saline
2013
Completed Phase 4
~2090

Find a Location

Who is running the clinical trial?

The Brooklyn Hospital CenterLead Sponsor
8 Previous Clinical Trials
2,067 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~7 spots leftby Apr 2025