{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,24]],"date-time":"2026-09-24T23:38:45Z","timestamp":1790293125317,"version":"4.1.0"},"reference-count":20,"publisher":"Wiley","issue":"10","license":[{"start":{"date-parts":[[2015,6,22]],"date-time":"2015-06-22T00:00:00Z","timestamp":1434931200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/100015661","name":"UCB Pharma","doi-asserted-by":"crossref","id":[{"id":"10.13039\/100015661","id-type":"DOI","asserted-by":"crossref"}]},{"name":"Mahnaz Asgharnejad"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Euro J of Neurology"],"published-print":{"date-parts":[[2015,10]]},"abstract":"<jats:sec><jats:title>Background and purpose<\/jats:title><jats:p>Non\u2010motor symptoms (<jats:styled-content style=\"fixed-case\">NMS<\/jats:styled-content>) of Parkinson's disease (<jats:styled-content style=\"fixed-case\">PD<\/jats:styled-content>) have a major impact on health\u2010related quality of life. This is the first randomized controlled trial to use the <jats:styled-content style=\"fixed-case\">NMS<\/jats:styled-content> Scale (<jats:styled-content style=\"fixed-case\">NMSS<\/jats:styled-content>) as a primary outcome to assess treatment effects on <jats:styled-content style=\"fixed-case\">NMS<\/jats:styled-content> in <jats:styled-content style=\"fixed-case\">PD<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>In this double\u2010blind trial (<jats:styled-content style=\"fixed-case\">NCT<\/jats:styled-content>01300819), patients with <jats:styled-content style=\"fixed-case\">PD<\/jats:styled-content> and a total <jats:styled-content style=\"fixed-case\">NMSS<\/jats:styled-content> score \u226540 were randomized (2:1) to rotigotine or placebo, titrated over 1\u20137\u00a0weeks to optimal dose (\u22648\u00a0mg\/24\u00a0h for patients not receiving levodopa, \u226416\u00a0mg\/24\u00a0h for patients receiving levodopa), maintained for 12\u00a0weeks. The primary outcome was change in <jats:styled-content style=\"fixed-case\">NMSS<\/jats:styled-content> total score from baseline to end of maintenance. Secondary outcomes were the nine <jats:styled-content style=\"fixed-case\">NMSS<\/jats:styled-content> domains, Unified Parkinson's Disease Rating Scale (<jats:styled-content style=\"fixed-case\">UPDRS<\/jats:styled-content>) <jats:styled-content style=\"fixed-case\">III<\/jats:styled-content> (motor) and the 39\u2010item Parkinson's Disease Questionnaire (<jats:styled-content style=\"fixed-case\">PDQ<\/jats:styled-content>\u201039).<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>In total, 283\/349 (81.1%) randomized patients completed the trial; 211 rotigotine and 122 placebo were included in the full analysis set. The <jats:styled-content style=\"fixed-case\">NMSS<\/jats:styled-content> total score decreased by 23 (rotigotine) and 19 (placebo) points; the treatment difference was not statistically significant (\u22123.58; 95% confidence interval \u22128.43, 1.26; <jats:italic>P\u00a0<\/jats:italic>=<jats:italic>\u00a0<\/jats:italic>0.147). Numerically greater than placebo improvements were detected in the \u2018mood\/apathy\u2019 and \u2018miscellaneous\u2019 <jats:styled-content style=\"fixed-case\">NMSS<\/jats:styled-content> domains (<jats:italic>P\u00a0<\/jats:italic>&lt;<jats:italic>\u00a0<\/jats:italic>0.05). Treatment differences in <jats:styled-content style=\"fixed-case\">UPDRS III<\/jats:styled-content> (\u22122.60; \u22124.27, \u22120.92; <jats:italic>P\u00a0<\/jats:italic>=<jats:italic>\u00a0<\/jats:italic>0.002) and <jats:styled-content style=\"fixed-case\">PDQ<\/jats:styled-content>\u201039 (\u22122.79; \u22125.21, \u22120.37; <jats:italic>P\u00a0<\/jats:italic>=<jats:italic>\u00a0<\/jats:italic>0.024) favoured rotigotine. Adverse events reported more frequently with rotigotine were nausea, application site reactions, somnolence and headache.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>Rotigotine improvement in the multi\u2010domain <jats:styled-content style=\"fixed-case\">NMSS<\/jats:styled-content> total score was not superior to placebo. A different sensitivity of individual <jats:styled-content style=\"fixed-case\">NMSS<\/jats:styled-content> domains to dopaminergic therapy and a large placebo effect may have contributed to these findings.<\/jats:p><\/jats:sec>","DOI":"10.1111\/ene.12757","type":"journal-article","created":{"date-parts":[[2015,6,22]],"date-time":"2015-06-22T05:29:15Z","timestamp":1434950955000},"page":"1400-1407","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":74,"title":["Effects of rotigotine transdermal patch in patients with Parkinson's disease presenting with non\u2010motor symptoms \u2013 results of a double\u2010blind, randomized, placebo\u2010controlled trial"],"prefix":"10.1111","volume":"22","author":[{"given":"A.","family":"Antonini","sequence":"first","affiliation":[{"name":"Parkinson and Movement Disorders Unit IRCCS Hospital San Camillo Venice Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"L.","family":"Bauer","sequence":"additional","affiliation":[{"name":"UCB Pharma Monheim am Rhein Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"E.","family":"Dohin","sequence":"additional","affiliation":[{"name":"UCB Pharma Paris France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"W. H.","family":"Oertel","sequence":"additional","affiliation":[{"name":"Department of Neurology Philipps University Marburg Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"O.","family":"Rascol","sequence":"additional","affiliation":[{"name":"Clinical Investigation Centre CIC1436 and Departments of Clinical Pharmacology and Neurosciences INSERM and Toulouse University Hospital Toulouse France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"H.","family":"Reichmann","sequence":"additional","affiliation":[{"name":"Department of Neurology University of Dresden Dresden Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M.","family":"Schmid","sequence":"additional","affiliation":[{"name":"UCB Pharma Monheim am Rhein Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"P.","family":"Singh","sequence":"additional","affiliation":[{"name":"UCB Pharma Monheim am Rhein Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"E.","family":"Tolosa","sequence":"additional","affiliation":[{"name":"Neurology Service Hospital Clinic de Barcelona Universitat de Barcelona IDIBAPS Centro de Investigacion Biomedica en Red sobre Enfermedades Neurodegenerativas (CIBERNED) Barcelona Catalonia Spain"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"K. 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