Autopsy report · NCT05633797
The Occurrence of Atrial Fibrillation After Totally Endoscopic Cardiac Surgery
Cause of deathStaffing, sites or logistics
“After the passing of the principal investigator, the clinical trial could not be continued.”
Life of this trial
- Registered 4 months before it started.
- Ran for about 1 year 8 months before it stopped.
- 152 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- Jessa Hospital
- Sponsor type
- University, hospital or other
- Conditions
- Atrial Fibrillation
- Interventions
- FibriCheck
- Participants
- 152
- Sites
- 1
- Countries
- Belgium
Trials that died the same way
- Novel Triple-dose Tuberculosis Retreatment Regimens: How to Overcome Resistance Without Creating More
“Feasibility of the clinical trial could not be confirmed at the different sites.” - A Dose Range Finding Study of JNJ-38518168 in Patients With Active Rheumatoid Arthritis in Spite of Treatment With Methotrexate
“The decision was made to prematurely discontinue this trial due to lack of efficacy.” - Accuracy of Robotically Assisted Cranial Biopsies
“The clinical study could not be commenced due to the Principal Investigator's limited availability, which has significantly impacted the feasibility of continuing the study as planned. No safety concerns or adverse events were detected.” - Acute Effects Of Donepezil On Brain Perfusion And Memory In Subjects With Cognitive Impairment And Mild Alzheimer's Disease
“The study was terminated because of slow enrollment. The decision to terminate the trial was not based on any safety or efficacy concerns.” - Study of a Melanoma Vaccine in Stage IIb, IIc, and III Melanoma Patients
“After interim analysis the study was halted to redesign a pivotal trial.”
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.