Discontinuation of Cholinesterase Inhibitors for the Treatment of Severe Alzheimer's Disease
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|ClinicalTrials.gov Identifier: NCT02035982|
Recruitment Status : Completed
First Posted : January 14, 2014
Last Update Posted : April 28, 2017
There are few pharmacological treatments available for Alzheimer's disease, including drugs called cholinesterase inhibitors: donepezil, galantamine, and rivastigmine. In research trials, cholinesterase inhibitors have been shown to improve memory and problem behaviours in people with mild to moderate Alzheimer's disease. However, these benefits may not extend to the real-world when taking into account nursing home and health care costs. There is less information on the use of cholinesterase inhibitors in people with severe Alzheimer's disease. In Canada, only donepezil is recommended for the treatment of severe Alzheimer's disease. However, there is no information on whether the benefits that donepezil provides to people with severe Alzheimer's disease are sustained over the long term. Moreover, while the tolerability of cholinesterase inhibitors is generally acceptable, their use is not completely harmless. Common side effects include nausea, diarrhea, insomnia, vomiting, muscle cramping, fatigue and loss of appetite.
In Ontario, cholinesterase inhibitor users tend to remain on these medications for two years or more and often until death. The current cholinesterase inhibitor guidelines provide details on what medication should be used, when it should be started and how it should be monitored, but there is less clarity on when it is safe and appropriate to stop treatment. The cessation of cholinesterase inhibitors in patients no longer appearing to display any clear benefits may help to lower the risk of unpleasant side effects, lower the use of multiple medications, and reduce the costs of caring for individuals with Alzheimer's disease. However, the cessation of cholinesterase inhibitor therapy may run the risk of deterioration in memory, worsening or development of behavioural symptoms and the placement of additional demands on professional and unpaid caregivers.
There is a clear need for guidelines when to stop cholinesterase inhibitor treatment, especially for patients in whom the benefits of not be on the medication will outweigh the risks. The purpose of this study is to address this issue by collecting data which may be helpful in predicting which types of patients may benefit from stopping cholinesterase inhibitor treatment. Understanding when, and for whom, it is appropriate to stop cholinesterase inhibitor treatment will influence the field of pharmacology in the treatment of Alzheimer's disease.
|Condition or disease||Intervention/treatment||Phase|
|Alzheimer's Disease Dementia||Drug: Cholinesterase Inhibitor Drug: Placebo||Phase 3|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||40 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|
|Official Title:||A Discontinuation of Cholinesterase Inhibitors for the Treatment of Severe Alzheimer's Disease in Long Term Care Setting|
|Study Start Date :||July 2010|
|Actual Primary Completion Date :||May 2014|
|Actual Study Completion Date :||September 2015|
Active Comparator: Cholinesterase Inhibitor
Participants randomized into the cholinesterase inhibitor arm will continue receiving their cholinesterase inhibitor at the same dosage.
Drug: Cholinesterase Inhibitor
For participants randomized into the active treatment arm, they will be provided with the following study medications:
Donepezil - 5 mg or 10 mg Galantamine - 8 mg and 16 mg and 24 mg Rivastigmine - 1.5 mg and 3 mg
The type of study medication provided will depend on the type and dosage of the cholinesterase inhibitor they have been receiving for the last 3 months of their regular treatment. For example, if that have been taking Donepezil - 5 mg daily, they will continue on that same medication, dosage and frequency.
Other Name: Galantamine, Donepezil, Rivastigmine
Placebo Comparator: Placebo
Participants randomized into the placebo arm will be tapered off their cholinesterase inhibitor for the first 2 weeks. For the remaining 6 weeks of their study they will be receiving only placebo, and no cholinesterase inhibitor.
For participants randomized into the placebo intervention, placebo capsules will match capsules in the active intervention.
- Clinician's Global Impression of Change (CGIC) [ Time Frame: baseline (0 weeks), 4 and 8 weeks ]CGIC score is used as a measure of clinically meaningful change, as distinct from an instrument's ability to assess any change. This scale is completed by the clinician.
- Number of total adverse events [ Time Frame: 2, 4, and 8 weeks ]All emerging adverse events (AEs) will be noted and followed-up until resolution. The total number of adverse events within each intervention arm will be compared between groups.
- Neuropsychiatric Inventory - nursing home version (NPI-NH) [ Time Frame: baseline (0 weeks), 4 and 8 weeks ]The NPI-NH will allow us to monitor and assess the change in the following neuropsychiatric symptoms: delusions, hallucinations, agitation, depression/dysphoria, anxiety, euphoria/elation, apathy/indifference, disinhibition, irritability/lability, aberrant motor behaviour, sleep, and appetite/eating disorders.
- Severe Impairment Battery (SIB) [ Time Frame: baseline (0 weeks), 4 and 8 weeks ]The SIB will allow us to assess cognition our participant group, who are too impaired to complete other standard neuropsychological tests. The SIB will allow us to detect changes in different domains of cognition (social interaction, memory, orientation, language, attention, praxis, visuospatial ability, constrution and orientation to name).
- The Alzheimer's Disease Cooperative Study-Activities of Daily Living Inventory, modified for severe AD (ADCS-ADL-sev) [ Time Frame: baseline (0 weeks), 4 and 8 weeks ]ADCS-ADL-sev assesses functional capacity based on 19 questions assessing various activities of daily living
- Mini-Mental State Examination (MMSE) [ Time Frame: screening (-1 weeks), baseline (0 weeks), 2, 4 and 8 weeks ]The MMSE will assess the severity of cognitive impairment and will provide a measurement of change in cognitive impairment between assessments.
- Apathy Evaluation Scale (AES) [ Time Frame: baseline (0 weeks), 4 and 8 weeks ]AES is an 18-item scale measuring apathy resulting from brain-related pathology.
- Cohen-Mansfield Agitation Inventory (CMAI) [ Time Frame: baseline (0 weeks), 4 and 8 weeks ]The CMAI is a 29-point scale that measures agitation in two dimensions; verbal and physical, each of which having two poles, aggressive and non-aggressive. The degree of agitation will be compared within and between intervention groups.
- Cornell Depression Scale for Dementia (Cornell) [ Time Frame: baseline (0 weeks), 4 and 8 weeks ]The CSDD is a scale assessing signs and symptoms of major depression in patients with dementia. This scale is completed by the caregiver, not the patient. The scale encompasses areas of mood-related signs, behavioural disturbance, physical signs, cyclic functions, and ideational disturbance.
- Quality of Life in Late Stage Dementia (QUALID) [ Time Frame: baseline (0 weeks) and 8 weeks ]The QUALID is an 11 item questionnaire completed by the caregiver. This questionnaire rates the quality of life in persons with late stage Alzheimer's disease and other dementing illnesses.
- Udvalg for Kliniske Undersøgelser (UKU) side effect rating scale [ Time Frame: baseline (0 weeks), 2, 4 and 8 weeks ]The UKU is a 53 item scale measuring side effects related to the study medication. This scale accounts for psychic, neurologic, autonomic and other symptoms.
- Number of p.r.n (as needed) medications used to treat behavioural and psychological symptoms of dementia (BPSD) [ Time Frame: baseline (0 weeks), 2, 4 and 8 weeks. ]The number of p.r.n medications administered to the patient is calculated every two weeks.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02035982
|North York General Hospital|
|Toronto, Ontario, Canada, M2K1E1|
|Sunnybrook Health Sciences Centre|
|Toronto, Ontario, Canada, M4N 3M5|
|Principal Investigator:||Krista L. Lanctôt, PhD||Sunnybrook Research Institute|
|Principal Investigator:||Nathan Herrmann, MD||Sunnybrook Health Sciences Centre|