Autopsy report · NCT00839488
Comparison of Intravenous Pantoprazole and Famotidine for Stress Ulcer Prophylaxis
Cause of deathStaffing, sites or logistics
“the chief of GS left the hopsital and the successor did't want to keep on this study”
Life of this trial
- Registered 10 months after it had already started.
- Ran for about 1 year before it stopped.
- 6 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 4
- Sponsor
- Far Eastern Memorial Hospital
- Sponsor type
- University, hospital or other
- Conditions
- Stomach Ulcer
- Interventions
- pantoprazole 40 mg iv; famotidine 20 mg iv
- Participants
- 6
- Sites
- 1
- Countries
- Taiwan
Trials that died the same way
- Study of GSK3845097 in Previously Treated Participants With Advanced Synovial Sarcoma and Myxoid/Round Cell Liposarcoma
“The study was terminated due to a change in GSK's R\&D priorities.” - Lactobacillus Lozenges as Preventative Care in Low-grade Dysplasia
“The study did not start as a key co-investigator left the institution.”
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.