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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00000179
Other study ID # IA0003
Secondary ID 3U01AG010483-08S
Status Completed
Phase Phase 3
First received October 29, 1999
Last updated June 23, 2005

Study information

Verified date March 2005
Source National Institute on Aging (NIA)
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 50 Years and older
Eligibility 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

Study Design

Allocation: Randomized, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Trazodone

Haloperidol


Locations

Country Name City State
United States University of Michigan Ann Arbor Michigan
United States Emory University Atlanta Georgia
United States University Hospitals of Cleveland Cleveland Ohio
United States University of Kansas Medical Center Kansas City Kansas
United States University of Kentucky Lexington Kentucky
United States University of California, Los Angeles Los Angeles California
United States University of Miami Miami Florida
United States University of Minnesota Minneapolis Minnesota
United States Mount Sinai Medical Center New York New York
United States New York University Medical Center New York New York
United States Oregon Health Sciences University Portland Oregon
United States University of Rochester Rochester New York
United States University of California, San Diego San Diego California
United States Southern Illinois University Springfield Illinois
United States University of South Florida Tampa Florida
United States University of Massachusetts Worcester Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
National Institute on Aging (NIA)

Country where clinical trial is conducted

United States, 

References & Publications (1)

Teri L, Logsdon RG, Peskind E, Raskind M, Weiner MF, Tractenberg RE, Foster NL, Schneider LS, Sano M, Whitehouse P, Tariot P, Mellow AM, Auchus AP, Grundman M, Thomas RG, Schafer K, Thal LJ; Alzheimer's Disease Cooperative Study. Treatment of agitation in — View Citation

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