Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Department of Psychiatry, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
Alzheimers Dement. 2019 Nov;15(11):1427-1436. doi: 10.1016/j.jalz.2019.06.4946. Epub 2019 Oct 3.
Alzheimer's disease (AD) is a disabling, common cause of dementia, and agitation is one of the most common and distressing symptoms for patients with AD. Escitalopram for agitation in Alzheimer's disease (S-CitAD) tests a novel, clinically derived therapeutic approach to treat agitation in patients with AD.
S-CitAD is a NIH-funded, investigator-initiated, randomized, multicenter clinical trial. Participants receive a structured psychosocial intervention (PSI) as standard of care. Participants without sufficient response to PSI are randomized to receive 15 mg escitalopram/day or a matching placebo in addition to PSI. Primary outcome is the Modified Alzheimer's Disease Cooperative Study - Clinical Global Impression of Change (mADCS-CGIC).
S-CitAD will provide information about a practical, immediately available approach to treating agitation in patients with AD. S-CitAD may become a model of how to evaluate and predict treatment response in patients with AD and agitation as a neuropsychiatric symptom (ClinicalTrials.gov Identifier: NCT03108846).
阿尔茨海默病(AD)是一种使人丧失能力的常见痴呆症病因,激越则是 AD 患者最常见且最令人痛苦的症状之一。用于治疗阿尔茨海默病激越的依地普仑(S-CitAD)试验了一种新颖的、源自临床的治疗方法,旨在治疗 AD 患者的激越症状。
S-CitAD 是一项由美国国立卫生研究院(NIH)资助的、由研究者发起的、随机、多中心临床试验。参与者接受结构化的心理社会干预(PSI)作为标准护理。对于 PSI 反应不足的参与者,将被随机分配接受 15 毫克依地普仑/天或与 PSI 同时给予安慰剂。主要结局指标是改良阿尔茨海默病合作研究-临床总体印象变化量表(mADCS-CGIC)。
S-CitAD 将提供有关治疗 AD 患者激越的实用、现成方法的信息。S-CitAD 可能成为评估和预测 AD 患者激越作为神经精神症状的治疗反应的模型(临床试验标识符:NCT03108846)。