Alzheimer's Disease Clinical Trial
Official title:
Post Marketing Study of Escitalopram Versus Risperidone for the Treatment of Behavioral and Psychological Symptoms Amongst Alzheimer's Disease Patients
Behavioral and psychological symptoms of dementia (BPSD) are among the most distressing
manifestations of dementia. Pharmacotherapy is frequently used and especially in
institutional settings. Current guidelines recommend the use of second-generation
antipsychotics (SGAs). Nonetheless, there are concerns regarding both their safety and
effectiveness in patients with dementia. Inconclusive evidence support the use of other
psychoactive agents such as SSRI antidepressants or cognitive enhancers.
In two published studies citalopram was as efficacious as, but better tolerated than
perphenazine or risperidone in patients with BPSD.
Thus, with proven efficacy and a beneficial safety profile the evaluation of the use of
escitalopram for BPSD is warranted.
Behavioral and psychological symptoms of dementia (BPSD) as agitation or psychosis are among
the most distressing manifestations of dementia. The evidence-based management of these
symptoms includes the search for treatable physical and environmental precipitants, support
and psychoeducation for primary caregivers and psychosocial interventions. Nevertheless,
pharmacotherapy is frequently used and especially in institutional settings. Current
guidelines recommend the use of second-generation antipsychotics (SGAs). Nonetheless, there
are concerns regarding both their safety and effectiveness in patients with dementia. Recent
research has resulted in a 'black-box" warning concerning the safety of using SGAs for BPSD.
Sparse and inconclusive evidence support the use of other psychoactive agents such as SSRI
antidepressants or cognitive enhancers.
In two published randomized controlled trials, citalopram was more efficacious than placebo
and as efficacious as, but better tolerated than perphenazine or risperidone in patients
with dementia hospitalized for the treatment of agitation or psychosis.
Thus, with proven efficacy and a beneficial safety profile the evaluation of the use of
escitalopram for BPSD is warranted.
A 6-week parallel groups, randomized, controlled trial in patients with dementia
hospitalized because of behavioral symptoms will be conducted at the Abarbanel MHC.
Participants will be consecutively recruited on an inpatient unit. Randomization will be
based on a table of random numbers held centrally by an uninvolved physician.
The study will be of a "double-blind" design. All medications in identical packaging will be
distributed to the ward from a central pharmacy.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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