Autopsy report · NCT00315458
Buprenorphine Transdermal Patch in Subjects With Osteoarthritis Pain Requiring Opioids. Includes a 52-Week Safety Extension.
Cause of deathStaffing, sites or logistics
“Administrative reasons.”
Life of this trial
- Registered 2 years 4 months after it had already started.
- Ran for about 1 year 3 months before it stopped.
- 107 participants enrolled.
- Results were posted on the registry 5 years 6 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 3
- Sponsor
- Purdue Pharma LP
- Sponsor type
- Industry
- Conditions
- Osteoarthritis
- Interventions
- Buprenorphine transdermal patch; Placebo transdermal patch
- Participants
- 107
- Sites
- 48
- Countries
- United States
Trials that died the same way
- An Exploratory Study of BPS804 Treatment in Adult Patients With Type I, III or IV Osteogenesis Imperfecta
“Administrative Reason” - A Study to Evaluate the Efficacy and Safety of Micafungin Against Invasive Candidiasis or Candidemia
“Due to administrative reasons” - RP2/RP3 in Combination With Atezolizumab and Bevacizumab for the Treatment of Patients With CRC
“Business reasons.” - Clinical and Cost Effectiveness of Different Dressing Materials in Diabetic Foot Ulcers
“Due to administrative reason” - Effect of Timing of Tumor-Treating Fields Plus Short-Course Radiation
“Organizational reasons”
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.