Autopsy report · NCT03212716
Efficiency of Antagonist Drugs of the Cellular Transcriptomic Signature of Influenza A Virus Infection.
Cause of deathStaffing, sites or logistics
“rate of inclusion and study affected by covid-19 epidemic”
Life of this trial
- Registered 6 months before it started.
- Ran for about 4 years 4 months before it stopped.
- 85 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 2
- Sponsor
- University Hospital, Lille
- Sponsor type
- University, hospital or other
- Conditions
- Flu
- Interventions
- Oseltamivir; Diltiazem; Placebos
- Participants
- 85
- Sites
- 19
- Countries
- France
Trials that died the same way
- Ivermectin in Adults With Severe COVID-19.
“Lack of severe COVID-19 cases in the place of study” - The Use of a Point-of-care Thoracic Ultrasound Protocol for Hospital Medical Emergency Teams
“Slow inclusion rate (partly due to Covid-19)” - Novel SARS-CoV-2 Point-of-care Testing
“failure in enrolling eligible subjects during COVID-19 outbreaks” - Characterizing Biomarkers of Early Parkinson's Disease Progression (TREG)
“COVID-19 Research Restrictions” - High-frequency vs. Low-frequency vs. Sham DMPFC-rTMS for Bulimia and Anorexia Nervosa
“COVID-19 pandemic restrictions.”
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.