Clinical trial

Study to Evaluate the Efficacy of Modafinil Treatment in Patients With Attention…

NCT00343811 · Cephalon, Industry · Completed

Key facts

NCT number NCT00343811
Title Study to Evaluate the Efficacy of Modafinil Treatment in Patients With Attention Deficit Hyperactivity Disorder (ADHD) Who Are Responders to Modafinil Treatment
Official title A 6-week, Double-Blind, Placebo-Controlled, Parallel Group Randomized Withdrawal Study to Evaluate the Continued Efficacy of Modafinil Treatment in Dosages up to 425mg/Day in Patients With Attention-Deficit/Hyperactivity Disorder Who Are Responders to Modafinil Treatment, Followed by a 12-Month…
Lead sponsor Cephalon, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Attention Deficit Hyperactivity Disorder
Intervention type Drug
Interventions Modafinil
Enrollment 120
Start date Jun 1, 2006
Completion Sep 1, 2006
First posted Jun 23, 2006
Last update posted May 9, 2014
Countries United States

At a glance

  • 10–99 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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