This is a prospective study in a cohort of about 30 patients with Idiopathic Parkinson's disease, who will be evaluated with a clinical assessment and an oculometric examination during a time period with specific intervals. This study aims to evaluate the correlation between oculometric measures and clinical assessment over time.
Age range
18 Years – 85 Years
Sex
ALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Change of saccadic latency over time as evaluated during visits
Timeframe: 12 months
Change of anti-saccadic error rates over time as evaluated during visits
Timeframe: 12 months
Change of smooth pursuit speed over time as evaluated during visits
Timeframe: 12 months
Correlation between MDS-UPDRS score and its parts with saccadic latency
Timeframe: 12 months
Correlation between MDS-UPDRS score and its parts with anti-saccadic error rates
Timeframe: 12 months
Correlation between MDS-UPDRS score and its parts with smooth pursuit
Timeframe: 12 months