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Depression Study Clinical Trials Resources presented on Clinical Trials Search isn't meant to be a substitute for qualified health advice, visits or professional assistance with a real medical. We aren't doctors. Always consult your mD about Depression Study conditions. Clinical Trials Search.org is a website dedicated to listing clinical research studies in human subjects. Depression Study Clinical research trials and Depression Study health trials occur in a lot of of places throughout the United States of America. A clinical trial or clinical study is a research project with human volunteer subjects. Clinical drug trials and pharmaceutical clinical trials typically assess the effectivity of new does drugs. The role of the studies / projects is to resolve certain human healthcare questions. Clinical trials are a popular way for doctors, government agencies, and private sector corporations to detect remedies for all varieties of circumstances, such as Depression Study. Depression Study Clinical Trials and other clinical trials allow volunteers to obtain health treatment choices before they are available to the general public. Most times the human subjects recieve professional assistance for free of charge, and every now and again they are paid for their time. Sometimes there is a cost for a Depression Study clinical trial. Human subjects frequently get the finest healthcare available for their Depression Study condition. Risks are a reality, however, and may include extra or frequent physician visits, medical dangers (possibly life-threatening), and/or the treatment being uneffective. Trials are federally governed with strict guidelines to protect clinical trials patients.

Home > "D" Clinical Trials Conditions > Depression Study

Depression Study



Depression Study

For Condition: Major Depressive Disorder
Status: Completed
Sponsor(s): Sponsor Name Pending ,
Synopsis: A Placebo Controlled Study Evaluating Efficacy And Safety 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/65 Years
Genders: Both
Protocol Entry Criteria: Inclusion Criteria: (Patients must meet these requirements in order to be eligible for this study.) - Patients meet the diagnosis of Major Depressive Disorder (MDD) Exclusion Criteria: (Patients cannot meet these criteria in order to be eligible for this study.) - Patients with a primary diagnosis other than MDD - Patients with a history of schizophrenia, schizoaffective disorders, seizure disorders or bipolar affective disorder - Patients receiving formal psychotherapy or cognitive/behavioral therapy concurrently or in the 12 weeks prior to screening visit - Patient is actively suicidal - Patients who have a history of migraine headaches
Total Enrollment: 

Location and Contact Information:

Study Site
Austin,  Texas,  78756
United States
 

Study Site
Glen Burnie,  Maryland,  21061
United States
 

Study Site
Lake Jackson,  Texas,  77566
United States
 

Study Site
Denver,  Colorado,  80212
United States
 

Study Site
Jacksonville,  Florida,  32216
United States
 

Study Site
Kenilworth,  New Jersey,  07033
United States
 

Study Site
Nashville,  Tennessee,  37212
United States
 

Study Site
Clementon,  New Jersey,  08021
United States
 

Study Site
Richmond,  Virginia,  23294
United States
 

Study Site
El Centro,  California,  92243
United States
 

Study Site
San Marcos,  California,  92078
United States
 

Study Site
Atlanta,  Georgia,  30308
United States
 

Study Site
Miramichi,  New Brunswick,  E1V 3G5
Canada
 

Study Site
Farmington,  Connecticut,  06030
United States
 

Study Site
Salem,  Oregon,  97309
United States
 

Study Site
Marietta,  Georgia,  30060
United States
 

Study Site
Springfield,  Illinois,  62701
United States
 

Study Site
Markham,  Ontario,  L6B 1A1
Canada
 

Study Site
New Baltimore,  Michigan,  48047
United States
 

Study Site
Toronto,  Ontario,  M5T3A9
Canada
 

Study Site
Okemos,  Michigan,  48864
United States
 

Study Site
New York City,  New York,  10021
United States
 

Study Site
Lake Oswego,  Oregon,  97305
United States
 

Study Site
Irvine,  California,  92618
United States
 

Study Site
Toronto,  Ontario,  M5G 2C4
Canada
 

Study Site
Garden Grove,  California,  92845
United States
 

Study SIte
Houston,  Texas,  77007
United States
 

Study Site
Edmonton,  Alberta,  T6L 5X8
Canada
 

Study Site
Eugene,  Oregon,  97401
United States
 

Study Site
Durham,  North Carolina,  27710
United States
 

Study Site
New York City,  New York,  10024
United States
 

Study Site
Jacksonville,  Florida,  32257
United States
 

Study Site
San Antonio,  Texas,  78229
United States
 

Study Site
Quebec,  ,  G1R 2W8
Canada
 

Study Site
Winnipeg,  Manitoba,  R2H 2A6
Canada
 

Study Site
Libertyville,  Illinois,  60084
United States
 

Study Site
Sherbrooke,  Quebec,  J1H 4J6
Canada
 

Study Site
Las Vegas,  Nevada,  89146
United States
 

Study Site
Beverly Hills,  California,  90210
United States
 

Study Site
Stanford,  California,  94305
United States
 

Study Site
Lexington,  Kentucky,  40509
United States
 

Study Site
New York City,  New York,  10467
United States
 

Study Site
Kelowna,  British Columbia,  V1Y2H4
Canada
 

Study Site
Atlanta,  Georgia,  30329
United States
 

Study Site
Sydney,  Nova Scotia,  B1S2E9
Canada
 


Additional Information:
Study ID Numbers:
  NKD20006; 
Study Start Date: 
Record last reviewed: January 2004
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00048204

Other Major Depressive Disorder Studies:
1. Treatment for Adolescents With Depression Study (TADS)

2. Treatment of patients with Major Depressive disorder with an investigational compound

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

4. Study Of Adults With Depression

5. Pharmacologic Treatment of PTSD in Sexually Abused Children

Related Studies:

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Depression Study

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