Last updated: November 28, 2023
Sponsor: University College London Hospitals
Overall Status: Active - Recruiting
Phase
N/A
Condition
N/ATreatment
N/AClinical Study ID
NCT06151002
173275
Ages 18-90 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Formal diagnosis of Parkinson Disease
Exclusion
Exclusion Criteria:
- Confirmation that the individual carries a GBA variant (GBA positive). Theseindividuals will be referred to sister-study, RAPSODI.
- History of Parkinsonism (progressive supranuclear palsy, multiple system atrophy,traumatic, manganese toxicity, postencephalitic, vascular PD; drug induced PD;corticobasal degeneration)
- Individuals with another neurological disorder including: dementia, movementdisorders, and motor neurone disease.
- Individuals on drugs known to be associated with parkinsonism, including neurolepticagents (Amisulpride, Chlorpromazine Hydrochloride, Flupenthixol, FluphenazineHydrochloride, Haloperidol, Methotrimeprazine, Levomepromazine, Olanzapine,Oxypertine, Pericyazine, Perphenazine, Pimozide, Pipotiazine, Prochlorperazine,Promazine Hydrochloride, Reserpine, Risperidone, Sulpiride, Thioridazine,Trifluoperazine, Zuclopenthixol acetate, Zotepine), plus Bupropion, , Lithium,Methyldopa, Metoclopramide and Sodium Valproate).
Study Design
Total Participants: 4800
Study Start date:
February 15, 2020
Estimated Completion Date:
August 20, 2040
Study Description
Connect with a study center
University College London (UCL)
London, NW3 2PF
United KingdomActive - Recruiting
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