Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06904287

Effectiveness of Magnesium in Addition to Prochlorperazine for the Treatment of Migraines

Evaluating the Effectiveness of Magnesium in Addition to Prochlorperazine for the Treatment of Migraines in the Emergency Department

Status
Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Wake Forest University Health Sciences · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this research study is to find out if using magnesium in addition to prochlorperazine will help reduce your migraine pain.

Detailed description

The purpose of this prospective, randomized, double-blinded study is to compare the relative efficacy and safety of intravenous magnesium in conjunction with intravenous prochlorperazine in the treatment of migraines. Participants will be patients presenting to the Emergency Department with primary diagnosis of migraine.

Conditions

Interventions

TypeNameDescription
DRUGMagnesiumProchlorperazine 10 mg administered as an intravenous push over 2 minutes followed by magnesium 2 g administered as an intravenous bolus over a period of 20 minutes
DRUGPlaceboProchlorperazine 10 mg administered as an intravenous push over 2 minutes followed by placebo (normal saline)

Timeline

Start date
2025-12-16
Primary completion
2027-06-01
Completion
2027-06-01
First posted
2025-04-01
Last updated
2026-01-22

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT06904287. Inclusion in this directory is not an endorsement.