CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 208 enrolled
Drug / intervention
metoclopramide +2 moredrug
Likely dose
metoclopramide 10 milligramsfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01825941
NCT01825941Phase 4Completed

Diphenhydramine as Adjuvant Therapy for Acute Migraine. A Randomized Trial.

Montefiore Medical Center·interventional·Posted Apr 8, 2013·Updated Jul 31, 2018

In Brief

A Phase 4 clinical trial evaluating metoclopramide, diphenhydramine, and 1 other intervention for Migraine. Completed, enrolled 208 participants across 1 site.

Detailed Summary

Parenteral diphenhydramine is commonly used as adjuvant therapy for acute migraine despite the fact that data supporting this practice do not exist. The investigators propose a randomized double blind study to test the hypothesis that 50mg of intravenous diphenhydramine, when added to standard migraine therapy, will result in a greater rate of sustained headache relief than standard migraine therapy alone. For this study, standard migraine therapy will be 10mg of intravenous metoclopramide. Sustained headache relief is defined as achieving a headache level of "mild" or "none" within two hours and maintaining a level of "mild" or "none" for 48 hours. Patients who present to the Montefiore emergency room (Bronx, NY) with an acute migraine will be approached for participation. They will be screened for medication contra-indications and non-migraine etiologies of headache. The study will be randomized. Assignment will be concealed. Participants and researchers will be blinded. Efficacy outcomes and adverse events will be assessed every half hour for two hours in the Emergency Department and by telephone 48 hours after medication administration. A sample size calculation, based on pilot data, revealed the need for 374 participants. An interim analysis will be performed after 200 participants have been enrolled with the goal of assessing for lack of conditional power.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMigraine
CountriesUnited States
Collaborators--

Timeline

Phase 4CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedApr 8, 2013
Enrollment StartApr 1, 2013
Primary CompletionDec 1, 2014
TodayJul 2, 2026
Enrollment to primary: 1.7 yearsPosted 13.2 years ago

Interventions

metoclopramidedrug

10 milligrams, administered intravenously over 15 minutes

diphenhydraminedrug

50 milligrams, administered intravenously over 15 minutes

placebodrug