Intranasal Ketorolac Trial

Status Not yet recruiting

Clinical Trial Summary

The purpose of this study is to determine if intranasal (IN) Ketorolac in combination with oral Prochlorperazine and Diphenhydramine is non-inferior to current migraine management which involves use of intravenous (IV) Ketorolac and oral adjuncts Prochlorperazine and diphenhydramine for reducing pain intensity in children with migraine headaches. The investigators hypothesize that IN ketorolac combined with these oral adjuncts is non-inferior to IV ketorolac and oral adjuncts in reducing acute migraine headache pain by a minimum clinically significant difference within 60 minutes of administration.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06083571
Study type	Interventional
Source	Washington University School of Medicine
Contact	Carlee Lenehan, MD
Phone	3529018388
Email	carleel@wustl.edu
Status	Not yet recruiting
Phase	Phase 2
Start date	January 1, 2024
Completion date	January 1, 2026

View Details

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