La maladie de Parkinson au Canada (serveur d'exploration)

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Trial designs used to study neuroprotective therapy in Parkinson's disease

Identifieur interne : 000947 ( Istex/Corpus ); précédent : 000946; suivant : 000948

Trial designs used to study neuroprotective therapy in Parkinson's disease

Auteurs : Anthony E. Lang ; Eldad Melamed ; Werner Poewe ; Olivier Rascol

Source :

RBID : ISTEX:1F8441423F9E5A20B3681C5AA731F29E6D85371F

Abstract

There have been numerous trials conducted to evaluate putative disease‐modifying or neuroprotective treatments in Parkinson's disease. These trials have used several different study designs and outcome measures. Each of these has its own strengths and weaknesses. Confounding all studies is the potential symptomatic benefit that the treatment might have on the features of Parkinson's disease. In addition, patient‐related factors such as age of onset and the nature of the dominant symptoms may have important impacts that are often not addressed. Here we provide an overview of the various trial designs that have been used and emphasize the challenges faced in attempting to study neuroprotection in Parkinson's disease and the advances needed before this goal can be successfully achieved. © 2013 Movement Disorder Society

Url:
DOI: 10.1002/mds.24997

Links to Exploration step

ISTEX:1F8441423F9E5A20B3681C5AA731F29E6D85371F

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<p>There have been numerous trials conducted to evaluate putative disease‐modifying or neuroprotective treatments in Parkinson's disease. These trials have used several different study designs and outcome measures. Each of these has its own strengths and weaknesses. Confounding all studies is the potential symptomatic benefit that the treatment might have on the features of Parkinson's disease. In addition, patient‐related factors such as age of onset and the nature of the dominant symptoms may have important impacts that are often not addressed. Here we provide an overview of the various trial designs that have been used and emphasize the challenges faced in attempting to study neuroprotection in Parkinson's disease and the advances needed before this goal can be successfully achieved. © 2013 Movement Disorder Society</p>
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Nothing to report.</p>
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<titleInfo lang="en">
<title>Trial designs used to study neuroprotective therapy in Parkinson's disease</title>
</titleInfo>
<titleInfo type="abbreviated" lang="en">
<title>PD Neuroprotective Therapy: Trial Designs</title>
</titleInfo>
<titleInfo type="alternative" contentType="CDATA" lang="en">
<title>Trial designs used to study neuroprotective therapy in Parkinson's disease</title>
</titleInfo>
<name type="personal">
<namePart type="given">Anthony E.</namePart>
<namePart type="family">Lang</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Morton and Gloria Shulman Movement Disorders Clinic and the Edmond J Safra Program in Parkinson's Disease, Toronto Western Hospital, Ontario, Toronto, Canada</affiliation>
<affiliation>E-mail: lang@uhnres.utoronto.ca</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Eldad</namePart>
<namePart type="family">Melamed</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>The Norma and Alan Aufzien Chair for Resarch of Parkinson's Disease, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Werner</namePart>
<namePart type="family">Poewe</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Department of Neurology, Innsbruck Medical University, Innsbruck, Austria</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Olivier</namePart>
<namePart type="family">Rascol</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Clinical Investigation Center and Department of Clinical Pharmacology and Neurosciences, CIC9302 INSERM and UMR825, Toulouse University Hospital, University of Toulouse‐3, Toulouse, France</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
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<genre type="review-article" displayLabel="reviewArticle"></genre>
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<publisher>Blackwell Publishing Ltd</publisher>
<dateIssued encoding="w3cdtf">2013-01</dateIssued>
<dateCreated encoding="w3cdtf">2013-02-06</dateCreated>
<dateCaptured encoding="w3cdtf">2011-12-23</dateCaptured>
<dateValid encoding="w3cdtf">2012-03-14</dateValid>
<copyrightDate encoding="w3cdtf">2013</copyrightDate>
</originInfo>
<language>
<languageTerm type="code" authority="rfc3066">en</languageTerm>
<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
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<abstract>There have been numerous trials conducted to evaluate putative disease‐modifying or neuroprotective treatments in Parkinson's disease. These trials have used several different study designs and outcome measures. Each of these has its own strengths and weaknesses. Confounding all studies is the potential symptomatic benefit that the treatment might have on the features of Parkinson's disease. In addition, patient‐related factors such as age of onset and the nature of the dominant symptoms may have important impacts that are often not addressed. Here we provide an overview of the various trial designs that have been used and emphasize the challenges faced in attempting to study neuroprotection in Parkinson's disease and the advances needed before this goal can be successfully achieved. © 2013 Movement Disorder Society</abstract>
<subject>
<genre>keywords</genre>
<topic>Parkinson's disease</topic>
<topic>neuroprotection</topic>
<topic>disease modification</topic>
<topic>trial designs</topic>
</subject>
<relatedItem type="host">
<titleInfo>
<title>Movement Disorders</title>
</titleInfo>
<titleInfo type="abbreviated">
<title>Mov Disord</title>
</titleInfo>
<genre type="journal">journal</genre>
<subject>
<genre>article-category</genre>
<topic>Review</topic>
</subject>
<identifier type="ISSN">0885-3185</identifier>
<identifier type="eISSN">1531-8257</identifier>
<identifier type="DOI">10.1002/(ISSN)1531-8257</identifier>
<identifier type="PublisherID">MDS</identifier>
<part>
<date>2013</date>
<detail type="title">
<title>The Vatican Conference on Neuroprotection in Parkinson's Disease</title>
</detail>
<detail type="volume">
<caption>vol.</caption>
<number>28</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>1</number>
</detail>
<extent unit="pages">
<start>86</start>
<end>95</end>
<total>10</total>
</extent>
</part>
</relatedItem>
<identifier type="istex">1F8441423F9E5A20B3681C5AA731F29E6D85371F</identifier>
<identifier type="DOI">10.1002/mds.24997</identifier>
<identifier type="ArticleID">MDS24997</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2013 Movement Disorder SocietyCopyright © 2013 Movement Disorders Society</accessCondition>
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<recordContentSource>WILEY</recordContentSource>
</recordInfo>
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<serie></serie>
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