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Agitation in Alzheimer's Disease



Agitation in Alzheimer's Disease

For Condition: Alzheimer Disease
Status: Completed
Sponsor(s): National Institute on Aging (NIA) ,
Synopsis: Agitation affects 70 to 90 percent of patients with AD. Signs of agitation include verbal and physical aggressiveness, irritability, wandering, and restlessness. These behaviors often make caring for patients at home very difficult. Trazodone and haldol are two of the most commonly prescribed drugs for agitation in AD patients. Behavior management, a non drug approach, has been effective in reducing signs of agitation. Researchers have yet to compare the effectiveness of drug versus non drug therapy to treat agitation in AD patients and determine which is the best treatment. The Alzheimer's Disease Cooperative Study, with funding from the National Institute on Aging, is conducting an agitation treatment program at 21 sites in 16 States. This study will assess which of the above treatments is most effective.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Randomized, Double-Blind, Placebo Control
Minimum Age/Maximum Age: 50 Years/
Genders: Both
Protocol Entry Criteria: Inclusion Criteria: - Memory problem consistent with a probable diagnosis of Alzheimer's disease (AD) - Agitation symptoms for at least the past 2 weeks - Patient has caregiver who can participate - Patient lives in the same household as the caregiver
Total Enrollment: 

Location and Contact Information:

Overall Study Official:
LeonThal,  Principal Investigator,  University of California, San Diego

University of Miami
Miami,  Florida,  33140
United States
 

University Hospitals of Cleveland
Cleveland,  Ohio,  44120
United States
 

University of Rochester
Rochester,  New York,  14620
United States
 

University of Michigan
Ann Arbor,  Michigan,  48109
United States
 

Oregon Health Sciences University
Portland,  Oregon,  97201-3098
United States
 

Southern Illinois University
Springfield,  Illinois,  62702
United States
 

Mount Sinai Medical Center
New York City,  New York,  10029
United States
 

University of California, Los Angeles
Los Angeles,  California,  90095
United States
 

New York University Medical Center
New York City,  New York,  10016
United States
 

University of South Florida
Tampa,  Florida,  33162
United States
 

University of Kansas Medical Center
Kansas City,  Kansas,  66160
United States
 

University of Minnesota
Minneapolis,  Minnesota,  55455
United States
 

University of Massachusetts
Worcester,  Massachusetts,  01665
United States
 

University of California, San Diego
San Diego,  California,  92093-0949
United States
 

University of Kentucky
Lexington,  Kentucky,  40536
United States
 

Emory University
Atlanta,  Georgia,  30329
United States
 


Additional Information:
Study ID Numbers:
  IA0003;  3U01AG10483-08S2
Study Start Date: 
Record last reviewed: November 2002
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00000179

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