Autopsy report · NCT00808990
The Effect of Probiotics on Non Alcoholic Fatty Liver Disease
Cause of deathStaffing, sites or logistics
“Time table was unfulfilled due to incompetent research coordinator. Inaccurate results and No conclusions can be withdrawn”
Life of this trial
- Registered 4 years 2 months before it started.
- Ran for about 2 years 7 months before it stopped.
- 38 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1
- Sponsor
- Rabin Medical Center
- Sponsor type
- University, hospital or other
- Conditions
- Liver Disease
- Interventions
- BioFemale
- Participants
- 38
- Sites
- 1
- Countries
- Israel
Trials that died the same way
- Efficacy of Flomax to Improve Stone Passage Following Shock Wave Lithotripsy
“Due to frequent turnover of research coordinators and thus poor study accrual.” - Pembrolizumab + Idelalisib for Lung Cancer Study
“The study was terminated due to poor accrual.” - Safety and Tolerability of PNT001 in Patients With Acute Traumatic Brain Injury (TBI)
“The study was terminated due to administrative, non-safety related reasons.” - 24-hour IOP Fluctuation Profile Recorded With SENSIMED Triggerfish in Primary Open-angle Glaucoma (POAG) Patients After Cataract Surgery
“Due to staff departures we were unable to execute this study” - Maxi-Analgesic Osteoarthritis (OA) Study
“The study was withdrawn for administrative reason”
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.