Autopsy report · NCT02452255
Fenofibrate and Propranolol in Burn Patients
Cause of deathOther
“Shriner's Burn Hospital closed the study and access to study-related data is unavailable. We are unable to submit the additional information or results-data”
Life of this trial
- Registered 6 months before it started.
- Ran for about 3 years 8 months before it stopped.
- 18 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 2, Phase 3
- Sponsor
- The University of Texas Medical Branch, Galveston
- Sponsor type
- University, hospital or other
- Conditions
- Burn
- Interventions
- Fenofibrate; Placebo; Propranolol
- Participants
- 18
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Propranolol in Severely Burned Children
“At the request of the study site, this study has been closed and access to study-related data is unavailable. We are unable to submit the results-data.” - Prostate-Specific Membrane Antigen (PSMA) Radionuclide Therapy
“So far, we have not been able to collect meaningful data for these patients which also led to our decision to close this study before attempting write up and publish any results” - Adipose Derived SVF for Aero-digestive & Enterocutaneous Fistulae
“Study closed due to lack of patient enrollment.” - Autoantibodies in Breast Cancer Detection
“Study closed to enrollment and data and specimen collection due to lack of funding.” - Tricyclic Antidepressants (TCAs) on Gastric Emptying
“Futility; study coordinator left and were unable to continue data collection; missing data”
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.