Autopsy report · 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
Cause of deathDrug or device supply
“Stopped prematurely in 2008 due to IONSYS withdrawal off the market globally”
Life of this trial
- Registered 2 months after it had already started.
- Ran for about 1 month before it stopped.
- 13 participants enrolled.
- Results were posted on the registry 4 years 5 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 4
- Sponsor
- Janssen Cilag N.V./S.A.
- Sponsor type
- Industry
- Conditions
- Pain, Postoperative
- Interventions
- Fentanyl ITS
- Participants
- 13
- Sites
- 3
- Countries
- Belgium
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.