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Sumatriptan nasal spray: a dose‐ranging study in the acute treatment of migraine

1999; Wiley; Volume: 6; Issue: 1 Linguagem: Inglês

10.1046/j.1468-1331.1999.610043.x

1468-1331

Andreas Peikert, Werner J. Becker, Elizabeth Ashford, C Dahlöf, H. Hassani, R Salonen,

Olfactory and Sensory Function Studies

This multicentre, randomized, double‐blind, placebo‐controlled, parallel group dose‐ranging study compared the efficacy and tolerability of four doses of sumatriptan nasal spray (2.5, 5, 10 and 20 mg) with a placebo, in the acute treatment of a single migraine attack. In total, 544 patients received the study medication as a single spray in one nostril, to treat a single migraine attack in the clinic. Efficacy assessments included the measurement of headache severity, clinical disability, and the presence/absence of associated symptoms. The incidence of headache recurrence was also assessed. The three highest doses of sumatriptan (5 mg 49%, 10 mg 46%, 20 mg 64%) were significantly better than the placebo (25%) at providing headache relief (moderate or severe headache improving to mild or none) 120 min after treatment (P < 0.01). Also, the 20 mg dose was significantly superior to both the 10 and 5 mg doses at this time point (P < 0.05). The proportion of patients who were headache‐free 120 min after treatment, was also higher following 20 mg (42%) rather than following any other sumatriptan dose (14–24%, P < 0.005 20 vs 10 mg) or placebo (11%). Headache recurrence in patients who had responded to initial treatment was reported by 30–41% of patients who received sumatriptan, compared with 33% of patients in the placebo group. Sumatriptan nasal spray was well tolerated, the incidence of adverse events with each dose of sumatriptan being similar to the placebo (20–27 and 23%, respectively). Apart from bad/bitter taste, the events were comparable with those reported following sumatriptan treatment by other routes of administration.