MUltiple Sclerosis and Extract of Cannabis: results of the MUSEC trial
Objective Multiple sclerosis (MS) is associated with chronic symptoms, including muscle stiffness, spasms, pain and insomnia. Here we report the results of the Multiple Sclerosis and Extract of Cannabis (MUSEC) study that aimed to substantiate the patient based findings of previous studies. Patients...
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description | Objective Multiple sclerosis (MS) is associated with chronic symptoms, including muscle stiffness, spasms, pain and insomnia. Here we report the results of the Multiple Sclerosis and Extract of Cannabis (MUSEC) study that aimed to substantiate the patient based findings of previous studies. Patients and methods Patients with stable MS at 22 UK centres were randomised to oral cannabis extract (CE) (N=144) or placebo (N=135), stratified by centre, walking ability and use of antispastic medication. This double blind, placebo controlled, phase III study had a screening period, a 2 week dose titration phase from 5 mg to a maximum of 25 mg of tetrahydrocannabinol daily and a 10 week maintenance phase. The primary outcome measure was a category rating scale (CRS) measuring patient reported change in muscle stiffness from baseline. Further CRSs assessed body pain, spasms and sleep quality. Three validated MS specific patient reported outcome measures assessed aspects of spasticity, physical and psychological impact, and walking ability. Results The rate of relief from muscle stiffness after 12 weeks was almost twice as high with CE than with placebo (29.4% vs 15.7%; OR 2.26; 95% CI 1.24 to 4.13; p=0.004, one sided). Similar results were found after 4 weeks and 8 weeks, and also for all further CRSs. Results from the MS scales supported these findings. Conclusion The study met its primary objective to demonstrate the superiority of CE over placebo in the treatment of muscle stiffness in MS. This was supported by results for secondary efficacy variables. Adverse events in participants treated with CE were consistent with the known side effects of cannabinoids. No new safety concerns were observed. Trial registration number NCT00552604. |
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Here we report the results of the Multiple Sclerosis and Extract of Cannabis (MUSEC) study that aimed to substantiate the patient based findings of previous studies. Patients and methods Patients with stable MS at 22 UK centres were randomised to oral cannabis extract (CE) (N=144) or placebo (N=135), stratified by centre, walking ability and use of antispastic medication. This double blind, placebo controlled, phase III study had a screening period, a 2 week dose titration phase from 5 mg to a maximum of 25 mg of tetrahydrocannabinol daily and a 10 week maintenance phase. The primary outcome measure was a category rating scale (CRS) measuring patient reported change in muscle stiffness from baseline. Further CRSs assessed body pain, spasms and sleep quality. Three validated MS specific patient reported outcome measures assessed aspects of spasticity, physical and psychological impact, and walking ability. Results The rate of relief from muscle stiffness after 12 weeks was almost twice as high with CE than with placebo (29.4% vs 15.7%; OR 2.26; 95% CI 1.24 to 4.13; p=0.004, one sided). Similar results were found after 4 weeks and 8 weeks, and also for all further CRSs. Results from the MS scales supported these findings. Conclusion The study met its primary objective to demonstrate the superiority of CE over placebo in the treatment of muscle stiffness in MS. This was supported by results for secondary efficacy variables. Adverse events in participants treated with CE were consistent with the known side effects of cannabinoids. No new safety concerns were observed. Trial registration number NCT00552604.</description><identifier>ISSN: 0022-3050</identifier><identifier>EISSN: 1468-330X</identifier><identifier>DOI: 10.1136/jnnp-2012-302468</identifier><identifier>PMID: 22791906</identifier><identifier>CODEN: JNNPAU</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd</publisher><subject>Adolescent ; Adult ; Biological and medical sciences ; Double-Blind Method ; Dronabinol - therapeutic use ; Female ; Humans ; Male ; Marijuana ; Medical sciences ; Middle Aged ; Multiple sclerosis ; Multiple Sclerosis - complications ; Multiple Sclerosis - drug therapy ; Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis ; Muscle pain ; Muscle Spasticity - complications ; Muscle Spasticity - drug therapy ; Muscle Tonus - drug effects ; Neurology ; Pain - drug therapy ; Patients ; Phytotherapy - methods ; Plant Extracts - therapeutic use ; Self Report ; Severity of Illness Index ; Sleep ; Sleep - drug effects ; Spasticity ; Tetrahydrocannabinol ; THC ; Walking</subject><ispartof>Journal of neurology, neurosurgery and psychiatry, 2012-11, Vol.83 (11), p.1125-1132</ispartof><rights>Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><rights>2015 INIST-CNRS</rights><rights>Copyright: 2012 Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b531t-f8700ddfd688ba94ecceb5e3a380b2e02265133b992b80476dab21a147caae8f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://jnnp.bmj.com/content/83/11/1125.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttps://jnnp.bmj.com/content/83/11/1125.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,776,780,3183,23550,27901,27902,77342,77373</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26493998$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22791906$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zajicek, John Peter</creatorcontrib><creatorcontrib>Hobart, Jeremy C</creatorcontrib><creatorcontrib>Slade, Anita</creatorcontrib><creatorcontrib>Barnes, David</creatorcontrib><creatorcontrib>Mattison, Paul G</creatorcontrib><creatorcontrib>MUSEC Research Group</creatorcontrib><creatorcontrib>on behalf of the MUSEC Research Group</creatorcontrib><title>MUltiple Sclerosis and Extract of Cannabis: results of the MUSEC trial</title><title>Journal of neurology, neurosurgery and psychiatry</title><addtitle>J Neurol Neurosurg Psychiatry</addtitle><description>Objective Multiple sclerosis (MS) is associated with chronic symptoms, including muscle stiffness, spasms, pain and insomnia. Here we report the results of the Multiple Sclerosis and Extract of Cannabis (MUSEC) study that aimed to substantiate the patient based findings of previous studies. Patients and methods Patients with stable MS at 22 UK centres were randomised to oral cannabis extract (CE) (N=144) or placebo (N=135), stratified by centre, walking ability and use of antispastic medication. This double blind, placebo controlled, phase III study had a screening period, a 2 week dose titration phase from 5 mg to a maximum of 25 mg of tetrahydrocannabinol daily and a 10 week maintenance phase. The primary outcome measure was a category rating scale (CRS) measuring patient reported change in muscle stiffness from baseline. Further CRSs assessed body pain, spasms and sleep quality. Three validated MS specific patient reported outcome measures assessed aspects of spasticity, physical and psychological impact, and walking ability. Results The rate of relief from muscle stiffness after 12 weeks was almost twice as high with CE than with placebo (29.4% vs 15.7%; OR 2.26; 95% CI 1.24 to 4.13; p=0.004, one sided). Similar results were found after 4 weeks and 8 weeks, and also for all further CRSs. Results from the MS scales supported these findings. Conclusion The study met its primary objective to demonstrate the superiority of CE over placebo in the treatment of muscle stiffness in MS. This was supported by results for secondary efficacy variables. Adverse events in participants treated with CE were consistent with the known side effects of cannabinoids. No new safety concerns were observed. Trial registration number NCT00552604.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Double-Blind Method</subject><subject>Dronabinol - therapeutic use</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Marijuana</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multiple sclerosis</subject><subject>Multiple Sclerosis - complications</subject><subject>Multiple Sclerosis - drug therapy</subject><subject>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</subject><subject>Muscle pain</subject><subject>Muscle Spasticity - complications</subject><subject>Muscle Spasticity - drug therapy</subject><subject>Muscle Tonus - drug effects</subject><subject>Neurology</subject><subject>Pain - drug therapy</subject><subject>Patients</subject><subject>Phytotherapy - methods</subject><subject>Plant Extracts - therapeutic use</subject><subject>Self Report</subject><subject>Severity of Illness Index</subject><subject>Sleep</subject><subject>Sleep - drug effects</subject><subject>Spasticity</subject><subject>Tetrahydrocannabinol</subject><subject>THC</subject><subject>Walking</subject><issn>0022-3050</issn><issn>1468-330X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkd-L1DAQx4Mo3nr67pMURBCkmh9Nk_gmdc9Tbv3BuSK-hEmaYtdsuyYpnP-9qV1P8OXmZWDmM8N35ovQQ4KfE8LqF7thOJQUE1oyTKta3kIrklPJGP56G60wpnOH4xN0L8YdnkOqu-iEUqGIwvUKnW22PvUH74pL610YYx8LGNpifZUC2FSMXdHAMIDp48siuDj5FOdi-u6KzfZy3RQp9ODvozsd-OgeHPMp2p6tPzfn5cWHN2-bVxel4YykspMC47bt2lpKA6py1jrDHQMmsaEuy605YcwoRY3ElahbMJQAqYQFcLJjp-jpsvcQxp-Ti0nv-2id9zC4cYqacE5qSoiSN6OUsooqwVVGH_-H7sYpDPkQTYQktBIK80zhhbL5TTG4Th9Cv4fwSxOsZzv0bIee7dCLHXnk0XHxZPauvR74-_8MPDkCEC34LsBg-_iPqyvF1J9jyoXrY3JX130IP3QtmOD6_ZdGb_C3dx_V60_6PPPPFt7sdzfL_A04v61K</recordid><startdate>20121101</startdate><enddate>20121101</enddate><creator>Zajicek, John Peter</creator><creator>Hobart, Jeremy C</creator><creator>Slade, Anita</creator><creator>Barnes, David</creator><creator>Mattison, Paul G</creator><general>BMJ Publishing Group Ltd</general><general>BMJ Publishing Group</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>7TK</scope></search><sort><creationdate>20121101</creationdate><title>MUltiple Sclerosis and Extract of Cannabis: results of the MUSEC trial</title><author>Zajicek, John Peter ; Hobart, Jeremy C ; Slade, Anita ; Barnes, David ; Mattison, Paul G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b531t-f8700ddfd688ba94ecceb5e3a380b2e02265133b992b80476dab21a147caae8f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Double-Blind Method</topic><topic>Dronabinol - therapeutic use</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Marijuana</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Multiple sclerosis</topic><topic>Multiple Sclerosis - complications</topic><topic>Multiple Sclerosis - drug therapy</topic><topic>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</topic><topic>Muscle pain</topic><topic>Muscle Spasticity - complications</topic><topic>Muscle Spasticity - drug therapy</topic><topic>Muscle Tonus - drug effects</topic><topic>Neurology</topic><topic>Pain - drug therapy</topic><topic>Patients</topic><topic>Phytotherapy - methods</topic><topic>Plant Extracts - therapeutic use</topic><topic>Self Report</topic><topic>Severity of Illness Index</topic><topic>Sleep</topic><topic>Sleep - drug effects</topic><topic>Spasticity</topic><topic>Tetrahydrocannabinol</topic><topic>THC</topic><topic>Walking</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zajicek, John Peter</creatorcontrib><creatorcontrib>Hobart, Jeremy C</creatorcontrib><creatorcontrib>Slade, Anita</creatorcontrib><creatorcontrib>Barnes, David</creatorcontrib><creatorcontrib>Mattison, Paul G</creatorcontrib><creatorcontrib>MUSEC Research Group</creatorcontrib><creatorcontrib>on behalf of the MUSEC Research Group</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database (ProQuest)</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Psychology Database (ProQuest)</collection><collection>ProQuest Science Journals</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Journal of neurology, neurosurgery and psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zajicek, John Peter</au><au>Hobart, Jeremy C</au><au>Slade, Anita</au><au>Barnes, David</au><au>Mattison, Paul G</au><aucorp>MUSEC Research Group</aucorp><aucorp>on behalf of the MUSEC Research Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MUltiple Sclerosis and Extract of Cannabis: results of the MUSEC trial</atitle><jtitle>Journal of neurology, neurosurgery and psychiatry</jtitle><addtitle>J Neurol Neurosurg Psychiatry</addtitle><date>2012-11-01</date><risdate>2012</risdate><volume>83</volume><issue>11</issue><spage>1125</spage><epage>1132</epage><pages>1125-1132</pages><issn>0022-3050</issn><eissn>1468-330X</eissn><coden>JNNPAU</coden><abstract>Objective Multiple sclerosis (MS) is associated with chronic symptoms, including muscle stiffness, spasms, pain and insomnia. Here we report the results of the Multiple Sclerosis and Extract of Cannabis (MUSEC) study that aimed to substantiate the patient based findings of previous studies. Patients and methods Patients with stable MS at 22 UK centres were randomised to oral cannabis extract (CE) (N=144) or placebo (N=135), stratified by centre, walking ability and use of antispastic medication. This double blind, placebo controlled, phase III study had a screening period, a 2 week dose titration phase from 5 mg to a maximum of 25 mg of tetrahydrocannabinol daily and a 10 week maintenance phase. The primary outcome measure was a category rating scale (CRS) measuring patient reported change in muscle stiffness from baseline. Further CRSs assessed body pain, spasms and sleep quality. Three validated MS specific patient reported outcome measures assessed aspects of spasticity, physical and psychological impact, and walking ability. Results The rate of relief from muscle stiffness after 12 weeks was almost twice as high with CE than with placebo (29.4% vs 15.7%; OR 2.26; 95% CI 1.24 to 4.13; p=0.004, one sided). Similar results were found after 4 weeks and 8 weeks, and also for all further CRSs. Results from the MS scales supported these findings. Conclusion The study met its primary objective to demonstrate the superiority of CE over placebo in the treatment of muscle stiffness in MS. This was supported by results for secondary efficacy variables. Adverse events in participants treated with CE were consistent with the known side effects of cannabinoids. No new safety concerns were observed. Trial registration number NCT00552604.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd</pub><pmid>22791906</pmid><doi>10.1136/jnnp-2012-302468</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Biological and medical sciences Double-Blind Method Dronabinol - therapeutic use Female Humans Male Marijuana Medical sciences Middle Aged Multiple sclerosis Multiple Sclerosis - complications Multiple Sclerosis - drug therapy Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis Muscle pain Muscle Spasticity - complications Muscle Spasticity - drug therapy Muscle Tonus - drug effects Neurology Pain - drug therapy Patients Phytotherapy - methods Plant Extracts - therapeutic use Self Report Severity of Illness Index Sleep Sleep - drug effects Spasticity Tetrahydrocannabinol THC Walking |
title | MUltiple Sclerosis and Extract of Cannabis: results of the MUSEC trial |
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