Efficacy of Rizatriptan 10 mg Administered Early in a Migraine Attack
- 24 May 2006
- journal article
- research article
- Published by Wiley in Headache: The Journal of Head and Face Pain
- Vol. 46 (6), 914-924
- https://doi.org/10.1111/j.1526-4610.2006.00466.x
Abstract
Objective.—To determine if administration of rizatriptan 10 mg is superior to placebo for the early treatment of acute migraine, while the pain is mild. Background.—Past studies have suggested that treatment outcomes can be improved if a triptan is administered early in the time course of a migraine attack. Methods.—Two randomized, parallel, placebo‐controlled, double‐blind studies. TAME (Treat A Migraine Early)1 was conducted at 46 centers in the United States; TAME2, at 48 centers in the United States. Totally, 1030 adult patients with at least a 6‐month history of migraine were studied. Patients were instructed to treat within 1 hour of migraine onset, while pain was mild. Patients maintained a headache diary in which they rated their levels of pain and disability, and recorded other symptoms of migraine. Primary endpoints were pain freedom at 2 hours and sustained pain freedom at 24 hours post‐dose. Results.—In TAME1, 57.3% versus 31.1% of patients reported pain freedom at 2 hours post‐dose and 42.6% versus 23.2% reported 24‐hour sustained pain freedom with rizatriptan versus placebo, respectively (P < .001 for both). In TAME2, 58.9% versus 31.1% of patients reported pain freedom at 2 hours post‐dose and 48.0% versus 24.6% reported 24‐hour sustained pain freedom with rizatriptan versus placebo, respectively (P < .001 for both). All other efficacy endpoints favored rizatriptan. Repeat doses of the medicine were not allowed; patients may have delayed treatment; non‐migraine headaches may have been treated. Conclusions.—Rizatriptan 10 mg was superior to placebo when treating migraine early, while pain is mild, as measured by pain freedom at 2 hours and 24‐hour sustained pain freedom.Keywords
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