Autopsy report · NCT00445263
Comparison of Two Treatment Strategies in Patients With an Acute Coronary Syndrome Without ST Elevation
Cause of deathSlow enrollment
“Because of inclusion delay”
Life of this trial
- Ran for about 6 years 4 months before it stopped.
- 170 participants enrolled.
- Results were posted on the registry 1 year 7 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 4
- Sponsor
- Hospital Avicenne
- Sponsor type
- University, hospital or other
- Conditions
- CORONARY DISEASE
- Interventions
- TIROFIBAN; CORONAROGRAPHY
- Participants
- 170
- Sites
- 1
- Countries
- France
Trials that died the same way
- Relapse Prevention With Escitalopram or Nortriptyline Following Electro-Convulsive Treatment (DUAG-7)
“Slow inclusion” - 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.” - Evaluating the Necessity of TOT Implantation in Women With Pelvic Organ Prolapse and Occult Stress Urinary Incontinence
“lack of inclusion” - Development of a Predictive Score for Local Complications of Femoral Bifurcation Surgery
“lack of inclusions” - Cutting Balloon Versus Non-cutting Balloon for the Treatment of Venous Stenosis in the Fistulas of Hemodialyzed Patients
“Inclusion curve too slow.”
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.