not generalizable to other RCTs. Goal Attainment Scaling (GAS); Global Measures. Clinician Interview-Based Impression of Change plus caregiver input ( CIBIC. interview [CIBIC-plus]). The ADAS- cog, disease assessment in dementia scale, and neuropsychiatric inventory are recorded by supervising site investigator, but . The Clinician Interview-Based Impression of Change, plus carer interview (CIBIC -Plus), is widely used in antidementia drug trials. It comprises Likert scales for.

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Several randomized, placebo-controlled trials have sought to evaluate the effect of latrepirdine on cognition, function and behaviour in patients with AD. Epub Oct This study aimed to assess the clinically variable ChEI treatment effects in a group of patients with mild AD using a semantic association and an N-back light working memory activation paradigm.

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The role of memantine as a treatment for Alzheimer’s disease AD has been controversial. This study examined the efficacy and safety of memantine monotherapy in scake with moderate-to-severe Alzheimer disease AD.

Huperzine A for Alzheimer’s disease. Patients were randomized to donepezil 10 mg daily or placebo for 24 weeks.

Donepezil has been used worldwide for the treatment of severe Alzheimer’s disease AD. Sixteen outpatients with a diagnosis of FTD were enrolled.

CIBIC Plus-J Assessment Using a Videotaped Method in Alzheimer’s Disease Patients

Donepezil treatment of patients with severe Alzheimer’s disease in a Japanese population: Dement Geriatr Cogn Dis Extra. Yet memantine is very frequently prescribed for mild AD and mild cognitive impairment, and a manufacturer-sponsored meta-analysis claimed its efficacy in mild AD. Murata, Azumi General Hospital. Memantine has been approved by the Food and Drug Administration for the treatment of moderate-to-severe Alzheimer’s disease AD.

Donepezil for dementia with Lewy bodies: J Am Geriatr Soc Jul 27;61 7: Slim J, Wright CC. Patients were randomised to either memantine or placebo in a 2: Dement Geriatr Cogn Disord 4;24 2: CNS Drugs Jun;27 6: Users may download, print and share scalr work on the Internet for noncommercial purposes only, provided the original work is properly cited, and a link to the original work on http: A report on the reliability of CIBIC plus-J described that eleven physicians who were familiar with dementia svale CGIC, videotaping the interviews of 13 AD patients and 7 virtual patients at baseline and after follow-up periods of 3—14 months.


CIBIC Plus-J Assessment Using a Videotaped Method in Alzheimer’s Disease Patients

Trials 06 8;17 1: We utilized cibiv AUC analysis to assess xibic cumulative treatment efficacy of memantine-donepezil combination versus component monotherapies on individual clinical domains and on a composite index.

Dement Geriatr Cogn Disord 5;40 We also wish to thank the following clinical research associates who were involved in collecting data for the study: In clinical trials, a high dropout rate and numerous adverse events associated with memantine have been observed.

However, this method is expected to be more appropriate than when local raters assess CIBIC plus-J at each site in mono-national clinical studies.

Whether it is also appropriate for severe AD in Chinese patients remains unknown. Epub Jan A 6-month, open-label study of memantine in patients with frontotemporal dementia.

A placebo-controlled, double-blind, comparative study of Galantamine hydrobromide in patients with Alzheimer-type dementia in Japanese. Memantine treatment in patients with mild to moderate Alzheimer’s disease: Effects of rivastigmine in Alzheimer’s disease patients with and without cigic.

J Am Med Dir Assoc 09 24;17 9: Because cholinergic deficits are prominent in dementia with Lewy bodies DLBwe investigated the effects of a cholinesterase inhibitor, donepezil, in such patients in a randomized, double-blind, placebo-controlled exploratory phase 2 trial.

Voices and visual images remained unretouched for the purpose of quality assurance. The global severity scales are clearly useful in subject categorization in treatment trials, in part because they are relatively free of many of the sociocultural biases inherent in mental status and psychometric descriptors.


A Randomized, Double-Blind Trial. Vascular cognitive impairment without dementia caused by subcortical ischemic small vessel disease hereinafter, subcortical Vascular cognitive impairment without dementia represents a relatively homogeneous disease process and is a suitable target for therapeutic trials investigating Vascular cognitive impairment without dementia.

Epub Jun To evaluate the efficacy and safety of rapidly titrated rivastigmine administered twice BID or three times TID daily in patients with mild to moderate Alzheimer’s disease AD.

A week, randomized, double-blind, placebo-controlled study to evaluate the efficacy, safety and tolerability of the rivastigmine patch in Japanese patients with Alzheimer’s disease. Okamoto, Department of Clinical Development, and the following statisticians who were involved in the statistical analysis: Voices of patients, caregivers, and CIBIC plus-J interviewers were recorded, and facial expressions of patients and caregivers were videotaped.

CIBIC-plus Publications | PubFacts

Effects of cholinesterase inhibitors in Parkinson’s disease dementia: Although this was a multicenter study, the precision of CIBIC plus-J assessment was also likely to be improved, because the total number of raters was decreased to seven central raters, with two raters assessing each patient.

Video Recording Voices of patients, caregivers, and CIBIC plus-J interviewers were recorded, and facial expressions of patients and caregivers were videotaped. This report is based on the data of a clinical trial that was sponsored by Dainippon Sumitomo Pharma Co. While the interrater reliability of CGIC has already been reported, that of the 3 subscales has not. Kundel HL, Palansky M.