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Deprexil in Subjects With Signs and Symptoms of Depression

Depression Clinical Trial

Official title:
Efficacy of Deprexil Administration in Subjects With Signs and Symptoms of Depression.

Clinical Trial Summary

The purpose of the study is to assess the efficacy of DEPREXIL administration in combination with relaxation psychotherapy in the treatment of patients with signs and symptoms of depression. The duration of this double-blind placebo controlled phase 3 clinical trial will be 24 weeks. The estimated number of persons to be recruited and randomized for the study is 200.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01043367
Study type Interventional
Source Catalysis SL
Contact
Status Completed
Phase Phase 3
Start date January 2010
Completion date January 2011
View Details
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