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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05709301
Other study ID # IIBSP-DON-2022-43
Secondary ID
Status Not yet recruiting
Phase Phase 2
First received
Last updated
Start date October 1, 2023
Est. completion date November 1, 2025

Study information

Verified date September 2023
Source Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Phase II, multi-centric, randomized, double-blinded, placebo-controlled, parallel design clinical trial to evaluate the safety, tolerability and efficacy of Donepezil in patients with Mild Cognitive Impairment in Parkinson's Disease (PD-MCI). A total of 120 patients with PD-MCI will be randomized to 12 months of oral Donepezil 10mg or matching placebo (1:1). Primary and co-primary efficacy endpoints are cognitive and functional cognitive scales: PD-CRS and PD-CFRS. Secondary efficacy endpoints include: cognitive tests evaluating attention, executive functions, language, memory and visuospatial domain; mood, anxiety, and apathy scales; questionnaires to evaluate quality of life; and subjective impression scales. Serum Neurofilament light chain, genetic screening of GBA, ApoE and MAPT, and Magnetic Resonance Imaging will be performed in a subset of these patients. The study will be conducted in 20 different centers around Spain. The Movement Disorders Unit of the Neurology Department at Sant Pau Hospital (Barcelona, Spain) will be the coordinating center.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 120
Est. completion date November 1, 2025
Est. primary completion date November 1, 2025
Accepts healthy volunteers No
Gender All
Age group 50 Years to 80 Years
Eligibility Inclusion Criteria: - Age 50-80 - PD diagnosis according to MDS criteria - Hoehn and Yahr stage I-III - Persistent subjective cognitive complaints for at least 6 months - MDS PD-MCI Level I and Level II criteria - Persistent PD-MCI for at least 3 months - Stable dopaminergic treatment for at least 1 month Exclusion Criteria: - PD dementia criteria - Severe motor complications - DBS or any brain condition that may be contributing to cognitive impairment - Active psychosis, major hallucinations, HADS =11, active impulse control disorder, or other active severe behavioral disorders. - Treatment under anticholinergics, cholinergic enhancers, or neuroleptics. - History of symptomatic arterial hypotension. - Hypersensitivity or intolerance to donepezil or any of the excipients - Pregnancy - Unstable medical or surgical condition - Any other significant observation that, in the investigator's opinion, would contraindicate participation in the study.

Study Design


Intervention

Drug:
Donepezil Hydrochloride
Donepezil 10mg once daily
Placebo
Matching placebo

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

Outcome

Type Measure Description Time frame Safety issue
Primary Parkinson's Disease-Cognitive Rating Scale (PD-CRS) Global cognition 12 months
Primary Parkinson's Disease-Cognitive Functional Rating Scale (PD-CFRS) Cognitive functional performance 12 months
Secondary Trail Making Test A (TMT-A) Attention 12 months
Secondary TMT-B Executive functions 12 months
Secondary Boston Naming Test Language 12 months
Secondary Free and cued selective reminding test Memory 12 months
Secondary Rey-Osterrieth complex figure test (ROCF) Visuospatial 12 months
Secondary Hospital Anxiety and Depression Scale Depression and Anxiety 12 months
Secondary Starkstein Apathy scale Apathy 12 months
Secondary Neuropsychiatric Inventory Hallucinations 12 months
Secondary Schwab & England scale Quality of life 12 months
Secondary Clinical Global Impressions-Severity of illness Subjective clinical change 12 months
Secondary CGI-Global improvement Subjective clinical change 12 months
Secondary Patient Global Impression of Change Subjective clinical change 12 months
Secondary 8-item Parkinson's Disease Questionnaire Quality of life 12 months
Secondary Judgment of Line Orientation Visuspatial 12 months
Secondary recall of ROCF Memory 12 months
Secondary Category fluency Language 12 months
Secondary Phonemic Fluency Executive functions 12 months
Secondary direct Digit Span Attention 12 months
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