drugset / Trial / NCT03836664

A Randomized Study Evaluating the Efficacy and Safety of Timolol Ophthalmic Solution as an Acute Treatment of Migraine

NCT03836664

Phase 2 Completed 25 enrolled University of Kansas Medical Center
RandomizedCrossoverDouble-blindTreatment

Summary

The purpose of this study is to assess the efficacy (headache freedom at 2 hours) of Timolol 0.5% ophthalmic solution compared to placebo in acute treatment of migraine headache. And to assess the safety and tolerability of Timolol 0.5% ophthalmic solution in treatment of acute migraine headache.

Timeline

Start
2017-02-27
Primary completion
2018-04-14
Completion
2018-04-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Timolol Other / unclassified 0.5 % Other

Indications