Autopsy report · NCT02662036
Analgesic Efficacy of Liposomal Bupivacaine vs. Bupivacaine HCL as a Tap Block After Abdominally Based Autologous Breast Reconstruction
Cause of deathFutility
“Interim analysis showed that there was no difference between the two drugs”
Life of this trial
- Registered 1 month before it started.
- Ran for about 2 years before it stopped.
- 70 participants enrolled.
- Results were posted on the registry 11 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 4
- Sponsor
- Washington University School of Medicine
- Sponsor type
- University, hospital or other
- Conditions
- Mammaplasty
- Interventions
- Bupivicaine HCL; Liposomal bupivacaine
- Participants
- 70
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Study of Immune Response Modifier in the Treatment of Hematologic Malignancies
“Drug was not available.” - Effectiveness of Periocular Drug Injection in CATaract Surgery
“Results of interim analysis: stop the trial due to one group being significantly different from the other three groups. Furthermore, shortage of study medication.” - Iontophoresis in Psoriasis
“FDA did not provide approval of the use of the drug for the study” - Bicalutamide and RO4929097 in Treating Patients With Previously Treated Prostate Cancer
“Drug was no longer available” - A Study of Maprotiline in Combination With Tamoxifen and Temozolomide for Recurrent Glioblastoma
“One of the drugs for the study is not commercially available.”
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.