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Clinical Trial Summary

The purposes of the study are to: 1) evaluate the short-term efficacy and safety of modafinil in atypical depression; and 2) to evaluate the efficacy of modafinil in preventing relapse of atypical depression. The hypothesis is that modafinil is safe and effective in the treatment of atypical depression.


Clinical Trial Description

This study on the safety and efficacy of modafinil on atypical depression has an initial 12-week open label treatment period with modafinil that is followed by a 12-week double-blind, randomized parallel treatment period with either modafinil or matching placebo. Patients who demonstrate at least minimal improvement after 12 weeks are randomly assigned to either continuing treatment at their current dose or switched to matching placebo for 12 weeks. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00215176
Study type Interventional
Source Duke University
Contact
Status Completed
Phase Phase 2/Phase 3
Start date February 2003
Completion date April 2005

See also
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Completed NCT00610506 - Escitalopram (Lexapro®) In Patients With Major Depression With Atypical Features Phase 3
Completed NCT00296699 - A Pilot Study Assessing Duloxetine's Efficacy in Atypical Depression Phase 4
Completed NCT00861978 - St. John's Wort Extract LI 160 for the Treatment of Atypical Depression Phase 3
Completed NCT00477854 - Effects of Chromium Picolinate on Food Intake N/A