Autopsy report · NCT02538822
Risk of Rupture of Aneurysms of the Thoracic Ascending Aorta (ATA) From the Dynamic Imaging
Cause of deathSlow enrollment
“low inclusion rates”
Life of this trial
- Registered 11 months after it had already started.
- Ran for about 3 years 11 months before it stopped.
- 31 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- Centre Hospitalier Universitaire de Saint Etienne
- Sponsor type
- University, hospital or other
- Conditions
- Aortic Aneurysm, Thoracic
- Interventions
- dynamic imaging; mechanical testing
- Participants
- 31
- Sites
- 1
- Countries
- France
Trials that died the same way
- The Dutch Asymptomatic Mitral Regurgitation Trial
“low inclusion rate” - PET / CT With 18F-FDG: Does it Optimize the I 123-MIBG Imaging Results in the Search for Discriminating Factors for the Implementation of an Implantable Defibrillator?
“Inclusion rate too slow / infeasible.” - Dexmedetomidine Pharmacokinetics-pharmacodynamics in Mechanically Ventilated Children With Single-organ Respiratory Failure
“Poor inclusion rate.” - Video-Assisted Thoracoscopic Pulmonary Vein Isolation Versus Percutaneous Catheter Ablation in Atrial Fibrillation Trial
“Inclusion rate insufficient” - Respiratory Variations for Assessing Blood Withdrawal 2
“insufficient inclusion rate”
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.