Cel
AChe I have been shown to afford modest benefits on cognition in AD patients. A systematic review by the Cochrane Collaboration states "the practical importance of these changes to patients is unclear" This study's primary objective is to find clinical evidence for the global efficacy of AChE I. The secondary aim is to develop a picture of the natural history of AD. These outcomes will provide a fundamental insight into the progression and treatment of AD aiding the formulation of European guidelines. This is a prospective 2 year observational study which co-ordinates the centralisation of patient data available within the individual centres. It does not require any modification in prescribing practice of participating centres. Patients will be recruited into either a treated or non-treated patient group and reviewed 6 monthly. The primary outcome measure is a deterioration of one level on the clinical dementia rating scale.
Dziedzina nauki
Zaproszenie do składania wniosków
Data not availableSystem finansowania
CON - Coordination of research actionsKoordynator
31300 TOULOUSE
Francja
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Uczestnicy (30)
LUXEMBOURG
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75013 PARIS
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08041 BARCELONA
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33076 BORDEAUX
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59037 LILLE
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4000 LIEGE
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34295 MONTPELLIER
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06002 NICE
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25125 BRESCIA
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T2H 2K6 CALGARY
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2100 KOEPENHAGEN
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37044 TOURS
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08014 BARCELONA
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37075 GOETTINGEN
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THESSALONIKI
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141 86 HUDDINGE
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SN1 4HZ SWINDON
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6500 HB NIJMEGEN
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92037-0624 SAN DIEGO
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BA2 5RP BATH
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28040 MADRID
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14071 CORDOBA
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31080 PAMPLONA
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06122 Perugia
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1226 THONEX
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16132 GENOVA
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M23 9LT MANCHESTER
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CV4 7AL COVENTRY
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1007 MB AMSTERDAM
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68072 Mannheim
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