Multi-centre UK Study of the Acetylcholinesterase Inhibitor Donepezil in Early Dementia Associated With Parkinson's Disease

Phase 3

Terminated

• Conditions: Parkinson's Disease
• Interventions: Drug: Donepezil

• Registration Number: NCT01014858
• Lead Sponsor: Newcastle-upon-Tyne Hospitals NHS Trust

Brief Summary

To demonstrate the superiority of donepezil over placebo in improving cognitive function, neuropsychiatric burden and functional ability in people with Parkinson's disease and mild dementia after 24 months of treatment.

To demonstrate the superiority of donepezil over placebo in improving patient and carer quality of life and to establish the cost-effectiveness of donepezil.

To determine the instrument most suitable for evaluating change in cognition in people with Parkinson's disease and mild dementia.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2009-11-16
• Study First Submitted QC: 2009-11-16
• Study First Posted: 2009-11-17
• Study Start: 2013-01
• Primary Completion: 2014-09
• Study Completion: 2014-09
• Status Verified: 2017-09
• Last Update Submitted: 2017-09-21
• Last Update Posted: 2017-09-25

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 64

Inclusion Criteria

1. A diagnosis of Parkinson's disease according to UK Parkinson's Disease Society Brain Bank Criteria. These criteria are in standard use throughout the NHS in the UK and were supported by the NICE guidelines.
2. People with mild dementia associated with PD, where the patient and/or their family have become aware of cognitive with or without behavioural symptoms that are causing functional impairment. "Dementia" will be defined according to recently published Movement Disorder Society Task Force criteria for dementia associated with Parkinson's Disease and "operationalised" using the Addenbrooke's Cognitive Examination (ACE-R). The ACE-R permits some description of the dementia profile and also quantifies global impairment. It is increasingly used by clinicians in the UK to identify demented subjects, is relatively quick to perform (15 minutes or so), requires no specific training and produces a total score (0-100), from which the MMSE (0-30) can also be extracted. Participants will have an ACE-R of 88 or less. If this criterion is met, subjects will be further assessed using the Mattis Dementia Rating Scale (DRS-2). An age- and education-corrected total DRS-2 score of less than 8 but greater than 4 (corresponding to between the 6th and 28th percentile) will be used to define "mild" dementia".
3. Community-living and a spouse, close relative or well established carer to accompany the subject to act as an informant.
4. Where relevant, women of child bearing potential must be using adequate contraception for duration of study.

Exclusion Criteria

1. Dementia that develops within one year of the onset of motor symptoms. The reason for this "one year rule" is to specifically exclude participants with Dementia with Lewy Bodies (DLB). This exclusion criterion is consistent with recommendations made in the Movement Disorder Society Dementia Task Force Diagnostic Criteria and the Third Report of the DLB Consortium.
2. People with such severe motor disability, or who are so impaired in their activities of daily living from other aspects of their PD, that it would interfere with cognitive and global assessments.
3. Severe current depressive episode. Low mood may impact upon accurate cognitive assessment and major depression is therefore listed as a feature which, when present, makes it impossible to reliably diagnose PDD in the Movement disorder Society Task Force PDD Criteria. This will be operationalised using the self-completed Beck Depression Inventory and a cut-off score of 13, as recommended by a recent Movement Disorder Society Task Force report. The BDI score is considered robust in the face of mild to moderate cognitive impairment.
4. Unstable significant medical co-morbidity.
5. Patient receiving an anticholinergic drug for control of parkinsonian motor symptoms.
6. Previous exposure to a cholinesterase inhibitor
7. Presence of a condition that is contraindicative to use of donepezil (including a clinically significant cardiac conduction defect found in patient history or from screening ECG); see SmPC (Appendix W) for details.
8. Allergy/hypersensitivity to excipients of donepezil or placebo
9. Patient receiving the N-methyl-d-aspartate antagonist memantine.
10. Previous neurosurgery for Parkinson's disease. This will apply to only a small minority of predominantly younger cases. The main reason for this exclusion relates to ongoing uncertainty over the potential confounding effects of deep brain stimulation upon both mood and cognition.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Donepezil	Donepezil	5mg of Donepezil for the first 8 weeks raising to 10mg thereafter if patient adjusted to 5mg dose. 10mg does continues for the remainder of the study.
Placebo	Donepezil	Patient commences medication to match appearance of 5mg donepezil for first 8 weeks then 10mg for the remainder of the study.

Primary Outcome Measures

Name	Time	Method
To demonstrate the superiority of donepezil over placebo in improving cognitive function, neuropsychiatric burden and functional ability in people with Parkinson's disease and mild dementia after 24 months of treatment.	After 24 month of treatment

Secondary Outcome Measures

Name	Time	Method
To demonstrate the superiority of donepezil over placebo in improving patient and carer quality of life and to establish the cost-effectiveness of donepezil.	26, 52 and 104 weeks

Trial Locations

Locations (22)

Newcastle; 🇬🇧 Newcastle Upon Tyne, Tyne and Wear, United Kingdom

Cambridge Centre for Brain Repair; 🇬🇧 Cambridge, United Kingdom

Royal Bournemouth & Christchurch Hospitals NHS Foundation Trust; 🇬🇧 Dorset, United Kingdom

Dr Lakmali Sugathapala; 🇬🇧 Derby, United Kingdom

Royal United Hospital (RUH) Bath NHS; 🇬🇧 Bath, United Kingdom

Dr Pippa Metcalf; 🇬🇧 Gloucester, United Kingdom

Pennine Acute Hospitals NHS Trust; 🇬🇧 Bury, United Kingdom

Milton Keynes; 🇬🇧 Milton Keynes, United Kingdom

Llandudno Hospital, Betsi Cadwaladr University Health Board & School of Medical Sciences; 🇬🇧 Llandudno, United Kingdom

Plymouth Hospitals NHS Trust; 🇬🇧 Plymouth, United Kingdom

Norfolk and Norwich University Hospitals NHS Foundation Trust; 🇬🇧 Norwich, United Kingdom

Sandwell and West Birmingham NHS Foundation Trust; 🇬🇧 Birmingham, United Kingdom

King's College Hospital NHS Foundtion Trust; 🇬🇧 London, United Kingdom

North Tyneside General Hospital; 🇬🇧 Northumberland, United Kingdom

Manchester Mental Health & Social Care NHS Trust; 🇬🇧 Manchester, United Kingdom

Oxford University Hospitals NHS Foundation Trust; 🇬🇧 Oxford, United Kingdom

Poole Hospital NHS Trust; 🇬🇧 Poole, United Kingdom

Dr Dhakam; 🇬🇧 Surrey, United Kingdom

Steps and Pines, Southmead Hospital; 🇬🇧 Bristol, United Kingdom

NHS Greater Glasgow and Clyde; 🇬🇧 Glasgow, United Kingdom

Royal Gwent Hospital; 🇬🇧 Newport, United Kingdom

Southampton General Hospital; 🇬🇧 Southampton, United Kingdom