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NCT00214955 · ClinicalTrials.gov registry record · Phase 3

Study to Evaluate the Efficacy and Safety of ORAVESCENT Fentanyl Citrate for the Management of Breakthrough Pain

A Phase 3 study, sponsored by Cephalon.

Completed
Registry status
Phase 3
Development phase
120
Enrollment target

NCT00214955: Completed Phase 3 study, sponsored by Cephalon.

NCT00214955 is a Phase 3 study that has completed, run by Cephalon. The registered enrollment target is 120 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (84% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00214955, a Phase 3 study, has completed, sponsored by Cephalon.

COMPLETED
Registry status
Phase 3
Development phase
120 participants
Enrollment target

Study Summary

A Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Efficacy and Safety of ORAVESCENT Fentanyl Citrate for the Management of Breakthrough Pain in Opioid-Tolerant Patients with Chronic Neuropathic Pain

Interventions

  • DRUG ORAVESCENT Fentanyl Citrate

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2005-09
Phase Phase 3
Cephalon

64 total trials

What the finished NCT00214955 record still lists

NCT00214955 is an interventional study that assigns participants to a tested intervention. The registered 120 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (84% lower).

The record links to 0 conditions, and to 1 intervention - of which ORAVESCENT Fentanyl Citrate is the first listed.

NCT00214955 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00214955 about?

NCT00214955 is a clinical study titled "Study to Evaluate the Efficacy and Safety of ORAVESCENT Fentanyl Citrate for the Management of Breakthrough Pain". A Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Efficacy and Safety of ORAVESCENT Fentanyl Citrate for the Management of Breakthrough Pain in Opioid-Tolerant Patients with Chronic Neuropathic Pain

What is the current status of trial NCT00214955?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 120 participants. The study started on 2005-09.

What interventions are being tested in trial NCT00214955?

The interventions under investigation include: ORAVESCENT Fentanyl Citrate (DRUG).

Who is sponsoring clinical trial NCT00214955?

This trial is sponsored by Cephalon, which has 64 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00214955's enrollment target sits among peer trials

120 1619th of 2000 higher than 361 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00214955, the US trial registry maintained by the National Library of Medicine. NCT00214955 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.