Clinical Trials Directory

Trials / Unknown

UnknownNCT00703430

Memantine on Aggression and Agitation of Alzheimer's Disease (AD)

The Effect of Memantine on Aggression and Agitation and Its Impact on Caregiver Burden of Patients With Alzheimer's Disease: A 12-week Open-label Study

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Peking University · Academic / Other
Sex
All
Age
50 Years
Healthy volunteers
Not accepted

Summary

Alzheimer's disease (AD), is associated with behavioral disturbances in approximately 50% of AD patients in Beijing. Agitation, and aggression specifically, is considered the most serious noncognitive symptom experienced in patients with dementia. Memantine is a recognized treatment for Alzheimer's disease either alone or in combination with cholinesterase inhibitors. Its efficacy in vascular dementia is also established. Family members continue to play a central role in home care for the demented elderly in China. This proposal is to conduct a study in Beijing, China to investigate the efficacy and safety of Memantine in the treatment of agitation and aggression in AD patients. In addition, this proposal aims to explore the impact of memantine on caregiver burden of AD patients in Chinese culture.

Conditions

Interventions

TypeNameDescription
DRUGMemantineInitially Memantine 5mg/day, titrated within the first month to a maintenance dose of 20mg/day, which is maintained for the following 2 months.

Timeline

Start date
2008-03-01
Primary completion
2013-12-01
Completion
2014-06-01
First posted
2008-06-23
Last updated
2013-01-25

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT00703430. Inclusion in this directory is not an endorsement.