Source:http://linkedlifedata.com/resource/pubmed/id/10692752
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2000-3-28
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pubmed:abstractText |
In this dose-ranging, randomised, multinational, multicentre, double-blind, placebo-controlled, parallel group study, 431 patients treated a single migraine attack with study medication: sumatriptan suppository 6 mg, 12.5 mg, 25 mg, 50 mg, 100 mg, or placebo. Patients were treated in the clinic with a single dose in suppository form. All doses of sumatriptan, except 6 mg, were significantly better than placebo (p < 0.004) and achieved similar rates of headache relief within two hours of dosing. The highest response rate was in the 25 mg group (72%) compared with placebo (37%) (p < 0.001). Fewer patients required rescue medication in the active groups (1% 100 mg to 13% 6 mg) compared with placebo (17%), and more patients were able to work and function normally two hours after dosing (41%, 100 mg; 20%, placebo). The overall incidence of adverse events was similar in the placebo, 6 mg and 12.5 mg groups (14-17%) but higher in the 25 mg, 50 mg and 100 mg groups (25%, 32% and 29% respectively). Analysis of plasma sumatriptan levels indicated rapid rectal absorption for all doses (median tmax = 1.0 hr). It is concluded that sumatriptan, in doses above 6 mg, is an effective and well tolerated treatment for acute migraine. From this study doses of 12.5 mg and 25 mg sumatriptan were identified as having the best efficacy/safety profile and were evaluated further.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1368-5031
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
53
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
593-8
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:10692752-Adolescent,
pubmed-meshheading:10692752-Adult,
pubmed-meshheading:10692752-Aged,
pubmed-meshheading:10692752-Dose-Response Relationship, Drug,
pubmed-meshheading:10692752-Double-Blind Method,
pubmed-meshheading:10692752-Female,
pubmed-meshheading:10692752-Humans,
pubmed-meshheading:10692752-Male,
pubmed-meshheading:10692752-Middle Aged,
pubmed-meshheading:10692752-Migraine Disorders,
pubmed-meshheading:10692752-Serotonin Receptor Agonists,
pubmed-meshheading:10692752-Sumatriptan,
pubmed-meshheading:10692752-Suppositories,
pubmed-meshheading:10692752-Treatment Outcome
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pubmed:year |
1999
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pubmed:articleTitle |
A dose-defining study of sumatriptan suppositories in the acute treatment of migraine.
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pubmed:affiliation |
Glaxo-Wellcome, Greenford, Middlesex, France.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Comparative Study,
Randomized Controlled Trial,
Multicenter Study
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