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Duloxetine Versus Placebo in the Prevention of Relapse of Major Depressive Disorder



Duloxetine Versus Placebo in the Prevention of Relapse of Major Depressive Disorder

For Condition: Depressive Disorder
Status: Completed
Sponsor(s): Eli Lilly and Company ,
Synopsis: The purpose of this study is to determine if duloxetine is effective when compared to placebo in preventing recurrence of major depressive disorder in patients who have responded to open-label duloxetine treatment.
Details:
Eligibility:
Study Type:
  Interventional, Treatment
Minimum Age/Maximum Age: 18 Years/
Genders: Both
Protocol Entry Criteria: Inclusion Criteria: - Signed the informed consent - Meet criteria for major depressive disorder without psychotic features. - Have a level of understanding sufficient to provide informed consent and to communicate with the investigator and site personnel. - Have had at least one other major depressive episode prior to the one being experienced at study entry. - You are reliable and agree to keep all appointments for clinic visits, tests and procedures required by the protocol. Exclusion Criteria: - You have had treatment with a drug within the last 30 days that has not received regulatory approval at the time of study entry. - Any women who are pregnant or breast feeding. - If you have any serious medical illnesses other than major depressive disorder. - If you have previously participated in a clinical trial for duloxetine. - Any previous or current diagnosis of bipolar, schizophrenia, or other psychotic disorders.
Total Enrollment: 

Location and Contact Information:

For information on a site near you, call our call center at 1-877-CTLILLY (1-877-285-4559)
Durham,  North Carolina, 
United States
 


Additional Information:
Study ID Numbers:
  4445; 
Study Start Date: May 2002
Record last reviewed: March 2003
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00036309

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