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Study of Duloxetine in Elderly Patients with Major Depressive Disorder - Article


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Duloxetine

Cymbalta


Clinical Trial: Study of Duloxetine in Elderly Patients with Major Depressive Disorder

This study is no longer recruiting patients.

Sponsored by: Eli Lilly and Company
Information provided by: Eli Lilly and Company

Purpose

A study of the safety and efficacy of duloxetine in elderly patients (greater than 65 years old) with major depressive disorder

Condition Treatment or Intervention Phase
Depression, Cognition
 Drug: Duloxetine
 Drug: "Investigational Drug"
Phase III

MedlinePlus consumer health information 

Study Type: Interventional
Study Design: Treatment

Eligibility

Ages Eligible for Study:  65 Years and above,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria: 1. You must be able to visit the doctor's office for clinic visits, tests, and procedures. 2. You must have been diagnosed with major depression, and have had at least one other episode in the past.

Exclusion Criteria: 1. You have a current or previous major psychiatric disorder other than depression, such as bipolar disorder, schizophrenia, or other psychotic disorder. 2. You have taken a drug within the last 30 days that has not been approved for use by governmental authorities.


Location Information


California
      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Chula Vista,  California,  United States

      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Rosemead,  California,  United States

      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Beverly Hills,  California,  United States

      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Menlow Park,  California,  United States

      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., San Francisco,  California,  United States

Connecticut
      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Cromwell,  Connecticut,  United States

      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Hamden,  Connecticut,  United States

Florida
      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Clearwater,  Florida,  United States

      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., St. Petersburg,  Florida,  United States

      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Winter Park,  Florida,  United States

      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Port Charlotte,  Florida,  United States

      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY(1-877-285-4559) or speak with your personal physician., West Palm Beach,  Florida,  United States

Indiana
      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Indianapolis,  Indiana,  United States

Kansas
      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Wichita,  Kansas,  United States

Louisiana
      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., New Orleans,  Louisiana,  United States

Maryland
      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Baltimore,  Maryland,  United States

Massachusetts
      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Belmont,  Massachusetts,  United States

      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Boston,  Massachusetts,  United States

Missouri
      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Chesterfield,  Missouri,  United States

      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Kansas City,  Missouri,  United States

      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., St. Louis,  Missouri,  United States

New Jersey
      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Clementon,  New Jersey,  United States

      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Toms River,  New Jersey,  United States

New Mexico
      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Albuquerque,  New Mexico,  United States

New York
      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Olean,  New York,  United States

Oklahoma
      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Oklahoma City,  Oklahoma,  United States

Pennsylvania
      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Philadelphia,  Pennsylvania,  United States

Rhode Island
      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Warwick,  Rhode Island,  United States

Tennessee
      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Johnson City,  Tennessee,  United States

      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Nashville,  Tennessee,  United States

Texas
      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Austin,  Texas,  United States

      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Houston,  Texas,  United States

      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Lake Jackson,  Texas,  United States

      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY(1-877-285-4559) or speak with your personal physician., Dallas,  Texas,  United States

Utah
      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Salt Lake City,  Utah,  United States

Washington
      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Seattle,  Washington,  United States

Wisconsin
      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., West Allias,  Wisconsin,  United States

      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Middleton,  Wisconsin,  United States

Puerto Rico
      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY (1-877-295-4559) or speak with your personal physician., Santurce,  Puerto Rico

      For additional information regarding investigative sites for this trial, contact the Clinical Trials Support Center at 1-877-CTLILLY(1-877-285-4559) or speak with your personal physician., Ponce,  Puerto Rico

More Information

Study ID Numbers:  6091
Record last reviewed:  July 2004
Last Updated:  October 13, 2004
Record first received:  June 10, 2003
ClinicalTrials.gov Identifier:  NCT00062673
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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August 21, 2008



Page Updated: June 1, 2005
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