Simvastatin as a neuroprotective treatment for Parkinson's disease (PD STAT): protocol for a double-blind, randomised, placebo-controlled futility study.
Disease Progression
Dose-Response Relationship, Drug
Double-Blind Method
Drug Monitoring
/ methods
Drug-Related Side Effects and Adverse Reactions
/ diagnosis
Female
Humans
Interviews as Topic
/ methods
Male
Middle Aged
Neurologic Examination
/ methods
Neuroprotective Agents
/ administration & dosage
Outcome Assessment, Health Care
Parkinson Disease
/ diagnosis
Randomized Controlled Trials as Topic
Simvastatin
/ administration & dosage
MDS-UPDRS
Parkinson’s disease
neuroprotective effect
randomised controlled futility study
statin
Journal
BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874
Informations de publication
Date de publication:
07 10 2019
07 10 2019
Historique:
entrez:
10
10
2019
pubmed:
9
10
2019
medline:
24
10
2020
Statut:
epublish
Résumé
Parkinson's disease (PD) is a progressive neurodegenerative condition affecting approximately 185,000 people in the UK. No drug has been proven to slow disease progression. Epidemiological and pre-clinical data support simvastatin, a widely used cholesterol-lowering drug with a well-established safety profile, having neuroprotective properties. The aim of this study (Simvastatin as a neuroprotective treatment for PD (PD STAT)) is to determine whether simvastatin has the potential to slow PD progression. The study is part of the International Linked Clinical Trials initiative coordinated by The Cure Parkinson's Trust. This paper describes the protocol for the PD STAT study. PD STAT is a double-blind, randomised, placebo-controlled, multi-centre, parallel group, futility trial in patients with PD of mild-moderate severity. 235 participants have been recruited and randomly allocated in a 1:1 ratio to receive either oral simvastatin or matched placebo. Treatment involves a 1-month low-dose phase (40 mg daily), followed by a 23-month high-dose phase (80 mg daily) and ends with a 2-month washout period. Participants are reviewed at clinic visits at 1 month, 6, 12, 18, 24 and 26 months post-baseline, with interim telephone follow-up to monitor for adverse events.The primary outcome is the change in the Movement Disorder Society Unified Parkinson's Disease Rating Scale part III motor subscale score in the practically defined OFF medication state (OFF state) between baseline and 24 months. Primary analysis will be on a modified intention to treat basis and will include only those participants who progress to the high-dose phase of the study. The protocol has been approved by the North East-Newcastle and North Tyneside 2 Research Ethics Committee. The results will be disseminated via research articles in peer-reviewed journals and presentations at local, national and international scientific meetings, as well as disseminated via patient groups, websites and networks. A summary of the study findings will be posted to participants at the end of the study. ISRCTN16108482 (prospectively registered); EudraCT 2015-000148-40; ClinicalTrials.gov NCT02787590; Pre-results.
Identifiants
pubmed: 31594876
pii: bmjopen-2019-029740
doi: 10.1136/bmjopen-2019-029740
pmc: PMC6797358
doi:
Substances chimiques
Neuroprotective Agents
0
Simvastatin
AGG2FN16EV
Banques de données
ClinicalTrials.gov
['NCT02787590']
ISRCTN
['ISRCTN16108482']
EudraCT
['2015-000148-40']
Types de publication
Clinical Trial Protocol
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e029740Informations de copyright
© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: RW is Director of Research and Development at The Cure Parkinson’s Trust.
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