TOPHAT (Trial of Ondansetron as a Parkinson's HAllucinations Treatment) is a double blind, individually randomized, placebo-controlled, parallel group, flexible dose trial of ondansetron (8-24mg/day) as a treatment for Parkinson's hallucinations, with a 12-week primary outcome and follow-up to 24 weeks.
This study investigates whether ondansetron, a drug used to treat post-operative sickness, has a meaningful treatment effect on Parkinson's hallucinations, and whether the drug is safe and cost effective for use in the NHS. We will compare ondansetron to placebo (a tablet that looks identical but contains no drug) over 12 weeks treatment, with follow up (once treatment ends) for a further 12 weeks. Assessments of symptoms will be carried out during treatment (after 6 and 12 weeks), and once treatment ends (18, 24 weeks), to measure hallucinations, delusions (false beliefs), Parkinson's symptoms (tremor, anxiety, sleep disturbance), memory, quality of life, possible side-effects such as constipation and headache, and the proportion of people who drop out due to side effects, or require additional treatment for their hallucinations. Blood drug concentration (measured after 6 and 12 weeks) will provide information on how quickly the drug is cleared from the body, and how this relates to treatment effects and side-effects, to guide future prescribing in people with Parkinson's. Based on knowledge of the average hallucinations scores in previous Parkinson's treatment studies, 306 people will be needed for the study to detect a meaningful treatment effect. The study will run for 4 years and involves a series of linked stages: (1) Trial set up across 20-30 UK centres; (2) Recruitment over 2 years; (3) Completion of follow up; and analysis, publication and dissemination of results.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
168
Participants will take one tablet daily in weeks 1 and 2, two tablets daily in weeks 3 and 4 and 3 tablets daily in weeks 5 and 6. Dose escalation will be guided by tolerability, through telephone safety monitoring prior to each dose increase
Grampian
Aberdeen, United Kingdom
Betsi Cadwaladr
Bangor, United Kingdom
Hallucinations
Scale for Assessment of Positive Symptoms-Hallucinations (0-35 points, higher scores indicate greater severity of hallucinations
Time frame: 12 weeks
Delusions
Scale for Assessment of Positive Symptoms-Delusions (0-65 points, higher scores indicate greater symptom severity
Time frame: 2, 4, 6, 12, 18, 24 weeks
Safety and tolerability
Number of Participants With Treatment-Related Adverse Events
Time frame: 2, 4, 6, 12, 18, 24 weeks
Health related quality of life
EQ-5D-5L
Time frame: 6, 12, 18, 24 weeks
Cost effectiveness
Health and social service utilisation
Time frame: 2, 4, 6, 12, 18, 24 weeks
Pharmacokinetics, plasma concentrations of the study drug
Measured using a validated HPLC/MS assay
Time frame: 6, 12 weeks
Hallucinations
Scale for Assessment of Positive Symptoms-Hallucinations (0-35 points, higher scores indicate greater severity of hallucinations
Time frame: 2, 4, 6, 18, 24 weeks
Global illness severity
Clinical Global Impression of Severity Scale (1-7, higher scores indicate greater severity)
Time frame: 2, 4, 6, 12, 18, 24 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Pennine
Bury, United Kingdom
Addenbrookes
Cambridge, United Kingdom
Dartford
Dartford, United Kingdom
Tayside
Dundee, United Kingdom
Glasgow
Glasgow, United Kingdom
Barking
London, United Kingdom
Bart's Health
London, United Kingdom
Imperial College NHS
London, United Kingdom
...and 13 more locations
Non-motor symptoms
Non-motor symptoms scale (0-120, higher scores indicate greater severity
Time frame: 2,4,6,12,18,24 weeks
Cognition
Standardised Mini-Mental State Examination (0-30, higher scores indicate better performance)
Time frame: 12 weeks
Hallucinations
University of Miami Parkinson's disease Hallucinations Questionnaire (0-15, where higher scores indicate greater symptom severity)
Time frame: 6, 12 weeks
Feasibility and Acceptability of Video Consultation
The feasibility of video consultation will be measured at baseline, 6 and 12 weeks by the proportion of participants who were able to successfully attend on at least one occasion, the proportion who successfully attended all three assessments, and a Satisfaction questionnaire that allows both quantitative and qualitative information to be collected.
Time frame: baseline, 6 and 12 weeks