Clinical trial

Study to Evaluate the Efficacy and Safety of OraVescent Fentanyl Citrate…

NCT00343733 · Cephalon, Industry · Completed

Key facts

NCT number NCT00343733
Title Study to Evaluate the Efficacy and Safety of OraVescent Fentanyl Citrate Treatment for the Management of Breakthrough Pain in Opioid-Tolerant Patients With Noncancer-Related Chronic Pain
Official title A 12-Week Open-Label Study With 3 Within-Patient Double-Blind Placebo-Controlled Periods to Evaluate the Efficacy and Safety of OraVescent Fentanyl Citrate Treatment for the Management of Breakthrough Pain in Opioid-Tolerant Patients With Noncancer-Related Chronic Pain
Lead sponsor Cephalon, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Pain
Intervention type Drug
Interventions OraVescent Fentanyl
Enrollment 120
Start date Aug 1, 2006
Completion Jul 1, 2007
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.

About ClinicalTrials.gov studies

ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.

Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

Browse all ClinicalTrials.gov studies