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CompletedNCT01072929

A Study to Evaluate the Efficacy and Safety of Armodafinil Treatment as Adjunctive Therapy in Adults With Major Depression Associated With Bipolarity type I

Medication studyAges 18–65United States
The study in practice

Understand this study

Who was this study for?

This study was for people with depression. Listed age limits: 18 years to 65 years. Other eligibility criteria applied.

Listed locations
Birmingham and 39 more locationsSee all locations and recruitment
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Study clarity

Study information

Study start dateJanuary 2010
Recruitment status
Completed
Enrollment listed in the registry
433
Sponsor
Cephalon
Sponsor type
Unknown or unclear
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
United States
Age range
From 18 Years to 65 Years
Official registry ID
NCT01072929
Official title
Show the full official title

A Double-Blind, Placebo-Controlled, Parallel-Group, Fixed-Dosage Study to Evaluate the Efficacy and Safety of Armodafinil Treatment (150 and 200 mg/Day) as Adjunctive Therapy in Adults With Major Depression Associated With Bipolar I Disorder

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Recruitment & locations

Completed

Birmingham · Beverly Hills · Garden Grove

36 more locations
  • Imperial
  • Irvine
  • Oceanside
  • San Diego
  • Santa Ana
  • Temecula
  • Coral Springs
  • Fort Myers
  • Gainesville
  • Jacksonville
  • Lauderhill
  • Orlando
  • Tampa
  • Atlanta
  • Roswell
  • Naperville
  • Oak Brook
  • Park Ridge
  • Baltimore
  • Fall River
  • St Louis
  • Mount Laurel
  • Albuquerque
  • Brooklyn
  • New York
  • Rochester
  • Staten Island
  • Raleigh
  • Beachwood
  • Dayton
  • Salem
  • Media
  • Scranton
  • Charleston
  • Austin
  • Bellevue
FAQ

Questions about this study

Who is behind this study?

The study sponsor is Cephalon.

Did this study involve medication?

Yes. The study involved medication, including Armodafinil and Placebo.

Who was this study for?

This study was for people with depression. Listed age limits: 18 years to 65 years. Other eligibility criteria applied.

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