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Evaluation of the efficacy of intravenous acetaminophen in the treatment of acute migraine attacks: a double-blind, placebo-controlled parallel group multicenter study

Using a multi-center, randomized, double-blind, placebo controlled study design, these researchers investigated the effectiveness of intravenous acetaminophen (1000 mg) in the treatment of acute migraine attacks as an alternative to parenteral application of lysine acetylsalicylate or triptans. Migraine diagnosis was made according to the International Headache Society Classification. Sixty patients were included in three headache outpatient centers in Germany. In the acute migraine attack, patients were treated intravenously with either 1000 mg acetaminophen or placebo. The primary end point was pain-free after 2 hours. Secondary efficacy criteria were pain-free after 24 hours or pain relief after 2 hours and after 24 hours. With regard to the efficacy criteria, 37% of patients reported pain relief or painfree after two hours, 12 patients after treatment with acetaminophen and 10 patients after treatment with placebo. Out of these, 3 patients in the acetaminophen and 4 patients in the placebo group were painfree. After 24 hours, 86% of the patients reported pain relief: 24 treated with acetaminophen and 27 treated with placebo. The results indicate, that 1000 mg intravenous acetaminophen is not superior to placebo in treating severe acute migraine attacks. Leinisch E, Evers S, Kaempfe N, Kraemer C, Sostak P, Jurgens T, Straube A, May A. Pain. 2005 Sep 6.

PMID 16153780
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=16153780&query_hl=12

Credit: PubMed, developed by the National Center for Biotechnology Information (NCBI) at the National Library of Medicine (NLM).




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