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Duloxetine Versus Placebo in the Prevention of Relapse of Major Depressive Disorder Clinical Trials Info presented on Clinical Trials Search isn't intended to be a substitute for qualified medical advice, visits or professional assistance by using a real mD. We are not docs. Always confer with your physician about Duloxetine Versus Placebo in the Prevention of Relapse of Major Depressive Disorder conditions. Clinical Trials Search.org is a website committed to listing clinical research studies in human subjects. Duloxetine Versus Placebo in the Prevention of Relapse of Major Depressive Disorder Clinical research trials and Duloxetine Versus Placebo in the Prevention of Relapse of Major Depressive Disorder health trials occur in many of cities throughout the US. A clinical trial or clinical study is a research project with human volunteer subjects. Clinical drug trials and pharmaceutical clinical trials generally evaluate the effectivity of new does drugs. The intent of the studies / undertakings is to resolve particular human health questions. Clinical trials are a popular way for physicians, government agencies, and private sector companies to detect remedies for all sorts of conditions, including Duloxetine Versus Placebo in the Prevention of Relapse of Major Depressive Disorder. Duloxetine Versus Placebo in the Prevention of Relapse of Major Depressive Disorder Clinical Trials and other clinical trials permit volunteers to obtain healthcare treatment alternatives before they are available to the masses. Most times the participants undergo professional assistance for without cost, and occasionally they are compensated for their time. Occasionally there is a cost for a Duloxetine Versus Placebo in the Prevention of Relapse of Major Depressive Disorder clinical trial. Test subjects typically receive the most expert healthcare available for their Duloxetine Versus Placebo in the Prevention of Relapse of Major Depressive Disorder condition. Dangers are a reality, however, and may include more or frequent mD visits, healthcare dangers (perhaps life-endangering), and/or the treatment being ineffectual. Trials are federally regulated with rigid guidelines to protect clinical trials patients.

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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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