None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients diagnosed with Parkinson's disease 2. Amyloid deposition confirmed by Florbetaben positron emission tomography 3. Mild cognitive impairment or early dementia (Clinical Dementia Rating : 0.5 or 1) on neuropsychological tests 4. Adults aged 50-90 years
Exclusion criteria
Exclusion criteria: 1. Cases in which lecanemab administration is contraindicated (based on recommendations from the Korean Dementia Association) 2. Cases in which neuropathologies other than Parkinson's disease or Alzheimer's disease are suspected as the underlying disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in amyloid dposition on amyloid imaging scans after 18 months of lecanemab administration in the lecanemab adminstration group | — |
Secondary
| Measure | Time frame |
|---|---|
| Longitudinal changes in cognitive function;Longitudinal changes in parkinsonian motor deficits;Longitudinal changes in the plasma and cerebrospinal fluid biomarkers in the lecanemab administration group | — |
Countries
Korea, Republic of
Contacts
Yonsei University Health System, Severance Hospital