drugset / Trial / NCT00779038

Safety and Efficacy Study of Fentanyl Iontophoretic Transdermal System (ITS) for Management of Moderate to Severe Acute Pain in Participants Who Have Undergone Elective Spine or Orthopedic Surgery

NCT00779038 ↗

Phase 4 Terminated 13 enrolled Janssen Cilag N.V./S.A.
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate in daily clinical practice the safety and efficacy of fentanyl Iontophoretic Transdermal (through the skin) System (ITS) for management of moderate (medium level of seriousness) to severe (very serious) acute (a quick and severe) pain in participants who have undergone elective spine or orthopedic (related to bones) surgery.

Timeline

Start
2008-08
Primary completion
2008-09
Completion
2008-09

Outcome

Outcome not reported

Stopped: “Stopped prematurely in 2008 due to IONSYS withdrawal off the market globally”

Drugs

EvaluationDrugModalityDoseRoute
Subject Fentanyl Other / unclassified 40 ug Other

Indications

No indication recorded.