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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02444637
Other study ID # RACE_1.0
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date April 2015
Est. completion date March 2019

Study information

Verified date March 2021
Source National Neuroscience Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Rivastigmine, an acetylcholinesterase inhibitor which has been approved by FDA & HSA, is authorized for use in the treatment of mild to moderate dementia of the Alzheimer's type. In this trial, the investigators will be studying the effectiveness of Rivastigmine in subjects with AD and cerebrovascular disease.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date March 2019
Est. primary completion date March 2019
Accepts healthy volunteers No
Gender All
Age group 50 Years to 85 Years
Eligibility Inclusion Criteria: - Age between 50-85 years - Diagnosis of dementia of the Alzheimer's type according to the National Institute of Ageing-Alzheimer's Association Criteriah - MRI brain (with T2 or FLAIR sequences) performed within a 12 month period from time of recruitment demonstrating the presence of WMH of =2 on the Fazekas scale (Score range of 0-3 wherein a score of 1 indicates mild WMH, 2 indicates moderate WMH and 3 indicates severe WMH).i - Clinical Dementia Rating score of 1-2j - Mini-Mental State Examination (MMSE) scores of 12-26 inclusivek - English or Mandarin speaking, literate participants Exclusion Criteria: - Severe neurological, psychiatric or systemic disease which in the opinion of the clinician could interfere with trial assessments - The use of any investigational drugs, new psychotropic or dopaminergic agents, cholinesterase inhibitors or anti-cholinergic agents during the 4 weeks prior to recruitment - Known skin allergy or previous allergic reaction to Rivastigmine patch

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Rivastigmine


Locations

Country Name City State
Singapore National Neuroscience Institute Singapore

Sponsors (1)

Lead Sponsor Collaborator
National Neuroscience Institute

Country where clinical trial is conducted

Singapore, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Participants with Demonstrated Benefit in Global and Cognitive Measures 2 Years
Secondary Number of Participants with Adverse Events as a Measure of Safety and Tolerability 2 Years
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