Efficacy of 1,000 mg Effervescent Acetylsalicylic Acid and Sumatriptan in Treating Associated Migraine Symptoms
Recently a new effervescent acetylsalicylic acid (ASA) tablet with high buffering capacity has been developed. In this double-blind, 3-arm, multicenter, parallel-group study, 433 patients were treated either with 1,000 mg effervescent ASA or 50 mg encapsulated sumatriptan or placebo. The primary end...
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Veröffentlicht in: | European neurology 2004-01, Vol.52 (1), p.50-56 |
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description | Recently a new effervescent acetylsalicylic acid (ASA) tablet with high buffering capacity has been developed. In this double-blind, 3-arm, multicenter, parallel-group study, 433 patients were treated either with 1,000 mg effervescent ASA or 50 mg encapsulated sumatriptan or placebo. The primary endpoint was the percentage of patients with complete remission of the 3 accompanying symptoms nausea, photophobia and phonophobia within 2 h after intake of the study drug. 43.8% of patients treated with ASA, 43.7% of patients treated with sumatriptan and 30.9% of patients treated with placebo showed complete remission of all 3 accompanying symptoms (p < 0.05 for ASA and sumatriptan vs. placebo). Both active treatments were superior to placebo regarding the individual symptoms photophobia and phonophobia, but not for nausea. The percentage of patients with reduction in headache severity from moderate or severe to mild or no pain (secondary objective) was 49.3% for ASA, 48.8% for sumatriptan and 32.9% for placebo. All active treatments were superior to placebo (p < 0.05). 25.3, 24.4 and 14.5% of patients treated with ASA, sumatriptan or placebo were pain free at 2 h. Drug-related adverse events were reported in 3.9, 4.7 and 6.7% of patients treated with placebo, ASA or sumatriptan. The study showed that administration of effervescent ASA leads to remission of the migraine symptoms nausea, photophobia and phonophobia, reduces migraine headache and is comparable to sumatriptan. |
doi_str_mv | 10.1159/000079544 |
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In this double-blind, 3-arm, multicenter, parallel-group study, 433 patients were treated either with 1,000 mg effervescent ASA or 50 mg encapsulated sumatriptan or placebo. The primary endpoint was the percentage of patients with complete remission of the 3 accompanying symptoms nausea, photophobia and phonophobia within 2 h after intake of the study drug. 43.8% of patients treated with ASA, 43.7% of patients treated with sumatriptan and 30.9% of patients treated with placebo showed complete remission of all 3 accompanying symptoms (p < 0.05 for ASA and sumatriptan vs. placebo). Both active treatments were superior to placebo regarding the individual symptoms photophobia and phonophobia, but not for nausea. The percentage of patients with reduction in headache severity from moderate or severe to mild or no pain (secondary objective) was 49.3% for ASA, 48.8% for sumatriptan and 32.9% for placebo. All active treatments were superior to placebo (p < 0.05). 25.3, 24.4 and 14.5% of patients treated with ASA, sumatriptan or placebo were pain free at 2 h. Drug-related adverse events were reported in 3.9, 4.7 and 6.7% of patients treated with placebo, ASA or sumatriptan. The study showed that administration of effervescent ASA leads to remission of the migraine symptoms nausea, photophobia and phonophobia, reduces migraine headache and is comparable to sumatriptan.</description><identifier>ISSN: 0014-3022</identifier><identifier>EISSN: 1421-9913</identifier><identifier>DOI: 10.1159/000079544</identifier><identifier>PMID: 15240983</identifier><identifier>CODEN: EUNEAP</identifier><language>eng</language><publisher>Basel, Switzerland: Karger</publisher><subject>Adolescent ; Adult ; Aged ; Aspirin - analogs & derivatives ; Aspirin - therapeutic use ; Biological and medical sciences ; Demography ; Double-Blind Method ; Female ; Follow-Up Studies ; Humans ; Male ; Medical sciences ; Middle Aged ; Migraine Disorders - drug therapy ; Neurology ; Original Paper ; Sumatriptan - therapeutic use ; Time Factors ; Treatment Outcome ; Vasoconstrictor Agents - therapeutic use</subject><ispartof>European neurology, 2004-01, Vol.52 (1), p.50-56</ispartof><rights>2004 S. 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Karger AG, Basel</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-4135f7243a0c45c908593e6921e52a52933bb9417e8f26be7550930827255cc93</citedby><cites>FETCH-LOGICAL-c415t-4135f7243a0c45c908593e6921e52a52933bb9417e8f26be7550930827255cc93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,2430,27928,27929</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15973234$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15240983$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Diener, H.C.</creatorcontrib><creatorcontrib>Eikermann, A.</creatorcontrib><creatorcontrib>Gessner, U.</creatorcontrib><creatorcontrib>Göbel, H.</creatorcontrib><creatorcontrib>Haag, G.</creatorcontrib><creatorcontrib>Lange, R.</creatorcontrib><creatorcontrib>May, A.</creatorcontrib><creatorcontrib>Müller-Schwefe, G.</creatorcontrib><creatorcontrib>Voelker, M.</creatorcontrib><title>Efficacy of 1,000 mg Effervescent Acetylsalicylic Acid and Sumatriptan in Treating Associated Migraine Symptoms</title><title>European neurology</title><addtitle>Eur Neurol</addtitle><description>Recently a new effervescent acetylsalicylic acid (ASA) tablet with high buffering capacity has been developed. In this double-blind, 3-arm, multicenter, parallel-group study, 433 patients were treated either with 1,000 mg effervescent ASA or 50 mg encapsulated sumatriptan or placebo. The primary endpoint was the percentage of patients with complete remission of the 3 accompanying symptoms nausea, photophobia and phonophobia within 2 h after intake of the study drug. 43.8% of patients treated with ASA, 43.7% of patients treated with sumatriptan and 30.9% of patients treated with placebo showed complete remission of all 3 accompanying symptoms (p < 0.05 for ASA and sumatriptan vs. placebo). Both active treatments were superior to placebo regarding the individual symptoms photophobia and phonophobia, but not for nausea. The percentage of patients with reduction in headache severity from moderate or severe to mild or no pain (secondary objective) was 49.3% for ASA, 48.8% for sumatriptan and 32.9% for placebo. All active treatments were superior to placebo (p < 0.05). 25.3, 24.4 and 14.5% of patients treated with ASA, sumatriptan or placebo were pain free at 2 h. Drug-related adverse events were reported in 3.9, 4.7 and 6.7% of patients treated with placebo, ASA or sumatriptan. The study showed that administration of effervescent ASA leads to remission of the migraine symptoms nausea, photophobia and phonophobia, reduces migraine headache and is comparable to sumatriptan.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aspirin - analogs & derivatives</subject><subject>Aspirin - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Demography</subject><subject>Double-Blind Method</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Migraine Disorders - drug therapy</subject><subject>Neurology</subject><subject>Original Paper</subject><subject>Sumatriptan - therapeutic use</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Vasoconstrictor Agents - therapeutic use</subject><issn>0014-3022</issn><issn>1421-9913</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqF0d9rFDEQB_Agir1WH3wWJAgVhK7Nz83m8SitFlr60PZ5mcvNHqm72TPJCvvfN8cdVXwxEMKED99hGEI-cPaNc23PWTnGaqVekQVXglfWcvmaLBjjqpJMiCNynNJTKbU1zVtyxLVQzDZyQcbLrvMO3EzHjvKzEkSHDS2fGH9jchgyXTrMc5-g924ut9R-TSGs6f00QI5-myFQH-hDRMg-bOgypdF5yLimt34TwQek9_OwzeOQ3pE3HfQJ3x_eE_J4dflw8aO6uft-fbG8qZziOleKS90ZoSQwp7SzrNFWYm0FRy1ACyvlamUVN9h0ol6h0ZpZyRphhNbOWXlCvuxzt3H8NWHK7eDLOH0PAccptXVtpGlq8V8omGXW8F3i53_g0zjFUIZouVWF1FwX9HWPXBxTiti12-gHiHPLWbvbVfuyq2I_HQKn1YDrP_KwnAJODwCSg76LEJxPfzlrpJC7oI979xPiBuML2Ld5Bu6foR8</recordid><startdate>20040101</startdate><enddate>20040101</enddate><creator>Diener, H.C.</creator><creator>Eikermann, A.</creator><creator>Gessner, U.</creator><creator>Göbel, H.</creator><creator>Haag, G.</creator><creator>Lange, R.</creator><creator>May, A.</creator><creator>Müller-Schwefe, G.</creator><creator>Voelker, M.</creator><general>Karger</general><general>S. 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In this double-blind, 3-arm, multicenter, parallel-group study, 433 patients were treated either with 1,000 mg effervescent ASA or 50 mg encapsulated sumatriptan or placebo. The primary endpoint was the percentage of patients with complete remission of the 3 accompanying symptoms nausea, photophobia and phonophobia within 2 h after intake of the study drug. 43.8% of patients treated with ASA, 43.7% of patients treated with sumatriptan and 30.9% of patients treated with placebo showed complete remission of all 3 accompanying symptoms (p < 0.05 for ASA and sumatriptan vs. placebo). Both active treatments were superior to placebo regarding the individual symptoms photophobia and phonophobia, but not for nausea. The percentage of patients with reduction in headache severity from moderate or severe to mild or no pain (secondary objective) was 49.3% for ASA, 48.8% for sumatriptan and 32.9% for placebo. All active treatments were superior to placebo (p < 0.05). 25.3, 24.4 and 14.5% of patients treated with ASA, sumatriptan or placebo were pain free at 2 h. Drug-related adverse events were reported in 3.9, 4.7 and 6.7% of patients treated with placebo, ASA or sumatriptan. The study showed that administration of effervescent ASA leads to remission of the migraine symptoms nausea, photophobia and phonophobia, reduces migraine headache and is comparable to sumatriptan.</abstract><cop>Basel, Switzerland</cop><pub>Karger</pub><pmid>15240983</pmid><doi>10.1159/000079544</doi><tpages>7</tpages></addata></record> |
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subjects | Adolescent Adult Aged Aspirin - analogs & derivatives Aspirin - therapeutic use Biological and medical sciences Demography Double-Blind Method Female Follow-Up Studies Humans Male Medical sciences Middle Aged Migraine Disorders - drug therapy Neurology Original Paper Sumatriptan - therapeutic use Time Factors Treatment Outcome Vasoconstrictor Agents - therapeutic use |
title | Efficacy of 1,000 mg Effervescent Acetylsalicylic Acid and Sumatriptan in Treating Associated Migraine Symptoms |
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