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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of neurology, neurosurgery and psychiatry neurosurgery and psychiatry, 2012-11, Vol.83 (11), p.1125-1132
Hauptverfasser: Zajicek, John Peter, Hobart, Jeremy C, Slade, Anita, Barnes, David, Mattison, Paul G
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1132
container_issue 11
container_start_page 1125
container_title Journal of neurology, neurosurgery and psychiatry
container_volume 83
creator Zajicek, John Peter
Hobart, Jeremy C
Slade, Anita
Barnes, David
Mattison, Paul G
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.
doi_str_mv 10.1136/jnnp-2012-302468
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1551621198</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1223429759</sourcerecordid><originalsourceid>FETCH-LOGICAL-b531t-f8700ddfd688ba94ecceb5e3a380b2e02265133b992b80476dab21a147caae8f3</originalsourceid><addsrcrecordid>eNqFkd-L1DAQx4Mo3nr67pMURBCkmh9Nk_gmdc9Tbv3BuSK-hEmaYtdsuyYpnP-9qV1P8OXmZWDmM8N35ovQQ4KfE8LqF7thOJQUE1oyTKta3kIrklPJGP56G60wpnOH4xN0L8YdnkOqu-iEUqGIwvUKnW22PvUH74pL610YYx8LGNpifZUC2FSMXdHAMIDp48siuDj5FOdi-u6KzfZy3RQp9ODvozsd-OgeHPMp2p6tPzfn5cWHN2-bVxel4YykspMC47bt2lpKA6py1jrDHQMmsaEuy605YcwoRY3ElahbMJQAqYQFcLJjp-jpsvcQxp-Ti0nv-2id9zC4cYqacE5qSoiSN6OUsooqwVVGH_-H7sYpDPkQTYQktBIK80zhhbL5TTG4Th9Cv4fwSxOsZzv0bIee7dCLHXnk0XHxZPauvR74-_8MPDkCEC34LsBg-_iPqyvF1J9jyoXrY3JX130IP3QtmOD6_ZdGb_C3dx_V60_6PPPPFt7sdzfL_A04v61K</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1781247905</pqid></control><display><type>article</type><title>MUltiple Sclerosis and Extract of Cannabis: results of the MUSEC trial</title><source>MEDLINE</source><source>BMJ Journals - NESLi2</source><creator>Zajicek, John Peter ; Hobart, Jeremy C ; Slade, Anita ; Barnes, David ; Mattison, Paul G</creator><creatorcontrib>Zajicek, John Peter ; Hobart, Jeremy C ; Slade, Anita ; Barnes, David ; Mattison, Paul G ; MUSEC Research Group ; on behalf of the MUSEC Research Group</creatorcontrib><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><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&amp;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 &amp; Allied Health Database (ProQuest)</collection><collection>Health &amp; 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 &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Psychology Database (ProQuest)</collection><collection>ProQuest Science Journals</collection><collection>Nursing &amp; 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>
fulltext fulltext
identifier ISSN: 0022-3050
ispartof Journal of neurology, neurosurgery and psychiatry, 2012-11, Vol.83 (11), p.1125-1132
issn 0022-3050
1468-330X
language eng
recordid cdi_proquest_miscellaneous_1551621198
source MEDLINE; BMJ Journals - NESLi2
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T19%3A42%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=MUltiple%20Sclerosis%20and%20Extract%20of%20Cannabis:%20results%20of%20the%20MUSEC%20trial&rft.jtitle=Journal%20of%20neurology,%20neurosurgery%20and%20psychiatry&rft.au=Zajicek,%20John%20Peter&rft.aucorp=MUSEC%20Research%20Group&rft.date=2012-11-01&rft.volume=83&rft.issue=11&rft.spage=1125&rft.epage=1132&rft.pages=1125-1132&rft.issn=0022-3050&rft.eissn=1468-330X&rft.coden=JNNPAU&rft_id=info:doi/10.1136/jnnp-2012-302468&rft_dat=%3Cproquest_cross%3E1223429759%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1781247905&rft_id=info:pmid/22791906&rfr_iscdi=true