Autopsy report · NCT01845974
Atrial Pressure Electrophysiology Pilot Study
Cause of deathSafety
“Interim evaluation of data after internal safety report from sponsor.”
Life of this trial
- Ran for about 3 years 7 months before it stopped.
- 13 participants enrolled.
- Results were posted on the registry 1 year 2 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- Wake Forest University Health Sciences
- Sponsor type
- University, hospital or other
- Conditions
- Atrial Fibrillation
- Interventions
- ThermoCool® SF NAV Catheter; ThermoCool® catheter
- Participants
- 13
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Timing for Removal of Chest Tubes in Adult Cardiac Surgery
“Safety interim analysis” - Ponatinib in Newly Diagnosed Chronic Myeloid Leukemia (CML) (EPIC)
“Study terminated based on evaluation of safety data.” - A Pilot Study Comparing the Safety and Efficacy of Everolimus With Other Medicines in Recipients of ECD/DCD Kidneys
“Interim results suggested a concern for patient outcomes and safety” - Study of Ataluren (PTC124) in Hemophilia A and B
“Study was terminated early due to Sponsor decision and not reflective of adverse safety findings.” - Extension Study of ACE-031 in Subjects With Duchenne Muscular Dystrophy
“This study was terminated based on preliminary safety data.”
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.