Expired Study
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Durham, North Carolina


Purpose:

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.


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.


NCT ID:

NCT00036309


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Durham, North Carolina
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: December 16, 2017

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