PMID- 17334957 OWN - NLM STAT- MEDLINE DCOM- 20070706 LR - 20181113 IS - 0340-5354 (Print) IS - 0340-5354 (Linking) VI - 254 IP - 2 DP - 2007 Feb TI - Patient preference in migraine therapy. A randomized, open-label, crossover clinical trial of acute treatment of migraine with oral almotriptan and rizatriptan. PG - 242-9 AB - OBJECTIVE: To assess patient preference for almotriptan 12.5 mg vs rizatriptan 10 mg for the acute treatment of migraine. METHODS: Randomized, multicenter, open-label, crossover trial in which triptan-naive patients treated two moderate/severe migraine attacks, the first with one triptan and the second with the other: 183 patients took rizatriptan followed by almotriptan and 189 treated in the reverse order. Patient preference was assessed with a self-administered questionnaire. RESULTS: Of those recording a preference (209), 54.5% preferred almotriptan, but statistical significance was not achieved. The main reason for preference for one or the other triptan was efficacy: 43% of patients preferring almotriptan gave faster headache relief as the reason and 34% cited faster return to normal activities. The corresponding values for rizatriptan were 47% and 38%. A significantly greater proportion of those preferring almotriptan cited fewer adverse events (AEs) as the reason. Almotriptan and rizatriptan were of comparable efficacy and both treatments were well tolerated; 9% of patients experienced AEs probably or possibly related to study medication after almotriptan vs 14% after rizatriptan. Almotriptan was associated with a significantly lower incidence of triptan-associated AEs in triptan-naive patients (8.5% vs 18% with rizatriptan). CONCLUSION: Physicians should use information from meta-analyses and preference studies like this one to aid in the selection of a triptan with a high likelihood of providing rapid, sustained relief from pain coupled with an absence of AEs. About 55% of patients recording a preference in this trial preferred almotriptan, perhaps because of its combination of good efficacy and lower incidence of triptan-associated AEs. FAU - Diez, Fernando Iglesias AU - Diez FI AD - Department of Neurology, Hospital General Yague, Avda. Del Cid 96, 09005 Burgos, Spain. iglesias@hgy.es FAU - Straube, Andreas AU - Straube A FAU - Zanchin, Giorgio AU - Zanchin G LA - eng PT - Clinical Trial PT - Journal Article PT - Multicenter Study PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't DEP - 20070302 PL - Germany TA - J Neurol JT - Journal of neurology JID - 0423161 RN - 0 (Serotonin Receptor Agonists) RN - 0 (Triazoles) RN - 0 (Tryptamines) RN - 1O4XL5SN61 (almotriptan) RN - 51086HBW8G (rizatriptan) SB - IM MH - Administration, Oral MH - Adolescent MH - Adult MH - Aged MH - Cross-Over Studies MH - Female MH - Humans MH - Male MH - Meta-Analysis as Topic MH - Middle Aged MH - Migraine Disorders/*drug therapy MH - *Patient Satisfaction/statistics & numerical data MH - Serotonin Receptor Agonists/*therapeutic use MH - Single-Blind Method MH - Time Factors MH - Triazoles/*therapeutic use MH - Tryptamines/*therapeutic use EDAT- 2007/03/06 09:00 MHDA- 2007/07/07 09:00 CRDT- 2007/03/06 09:00 PHST- 2006/03/22 00:00 [received] PHST- 2006/07/11 00:00 [accepted] PHST- 2007/03/06 09:00 [pubmed] PHST- 2007/07/07 09:00 [medline] PHST- 2007/03/06 09:00 [entrez] AID - 10.1007/s00415-006-0352-3 [doi] PST - ppublish SO - J Neurol. 2007 Feb;254(2):242-9. doi: 10.1007/s00415-006-0352-3. Epub 2007 Mar 2.