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Study Of Adults With Depression



Study Of Adults With Depression

For Condition: Major Depressive Disorder
Status: No longer recruiting
Sponsor(s): Sponsor Name Pending ,
Synopsis: A Placebo Controlled Study Evaluating Efficacy, Safety and Tolerability of Medication in Patients with Major Depressive Disorder (MDD)
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Minimum Age/Maximum Age: 18 Years/64 Years
Genders: Both
Protocol Entry Criteria: Inclusion Criteria - Diagnosis of Major Depressive Disorder (MDD) - Duration of current depressive episode 12 weeks - 24 months - Patients can read and write at a level sufficient to provide a signed consent - If female, patients must be practicing an acceptable method of birth control Exclusion Criteria - Patients have other psychiatric disorders that would affect patient's response to treatment - Patients have not responded to two or more adequate courses of antidepressant therapy - Patients cannot be currently abusing illicit drugs or alcohol - Patients are not currently receiving psychotherapy - Patients have received electroconvulsive therapy within 6 months prior to screening - Patients are pregnant or lactating
Total Enrollment: 

Location and Contact Information:

Study Site
Lafayette,  Indiana,  47905
United States
 

Study Site
St. Charles,  Missouri,  63301
United States
 

Study Site
San Diego,  California,  92108
United States
 

Study Site
Boynton Beach,  Florida,  33437
United States
 

Study Site
Temecula,  California,  92591
United States
 

Study Site
Tampa,  Florida,  33613
United States
 

Study Site
Beverly Hills,  California,  90210
United States
 

Study Site
Rockville,  Maryland,  20852
United States
 

Study Site
Marietta,  Georgia,  30060
United States
 

Study Site
Jacksonville,  Florida,  32216
United States
 

Study Site
Nashville,  Tennessee,  37203
United States
 

Study Site
Libertyville,  Illinois,  60048
United States
 

Study Site
Winston Salem,  North Carolina,  27103
United States
 

Study Site
Washington D.C.,  District of Columbia,  20037
United States
 

Study Site
Oakbrook Terrace,  Illinois,  60181
United States
 

Study Site
Albuquerque,  New Mexico,  87108
United States
 

Study Site
Toledo,  Ohio,  43623
United States
 

Study Site
Indianapolis,  Indiana,  46202
United States
 

Study Site
San Antonio,  Texas,  78229
United States
 

Study Site
Shreveport,  Louisiana,  71101
United States
 

Study Site
Bellevue,  Washington,  98004
United States
 

Study Site
Memphis,  Tennessee,  38119
United States
 

Study Site
Cerritos,  California,  90703
United States
 


Additional Information:
Study ID Numbers:
  OHB20003; 
Study Start Date: 
Record last reviewed: January 2004
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00057226

Other Major Depressive Disorder Studies:
1. Treatment of Patients with Major Depressive Disorder with an Investigational Compound

2. Treatment of Patients with Major Depressive Disorder with an Investigational Compound

3. Brain Chemical Receptor Effects in Patients with Panic Disorder and Post-Traumatic Stress Disorder

4. Open Label Duloxetine Compassionate Use in Patients Who Have Completed a Previous Neuroscience Duloxetine Clinical Trial

5. Treatment Resistant Depression Study

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Study Of Adults With Depression

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