Autopsy report · NCT03858647
Electrode Placement and Audiologic Outcomes With the Advanced Bionics HiFocus L23 Electrode
Cause of deathStaffing, sites or logistics
“device under study complication-due to PI departure, study closed and will not reopen”
Life of this trial
- Ran for about 2 years 10 months before it stopped.
- 16 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Sponsor
- Vanderbilt University Medical Center
- Sponsor type
- University, hospital or other
- Conditions
- Sensorineural Hearing Loss
- Participants
- 16
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Noninvasive Cardiac Output Measurements in Patients With Pulmonary Hypertension Undergoing Right Heart Catheterization With Acute Vasodilator Testing
“The PI closed this study and went to another institution.” - Randomized Controlled Trial (RCT) Umbilical Hernia Repair (UHR) Absorbable vs Non-absorbable Synthetic Mesh
“study was never opened and PI now leaving institution” - Autologous Platelet Gel in Wound Healing of Coronary Artery Bypass Grafting (CABG) Patients
“Study closed with no subjects accrued. PI decided to stop study.” - Assessment of Primary and Metastatic Brain Tumor Hypoxia With Fluoromisonidazole, FDG and Water
“PI retired, study closed” - Non-Invasive Measurement of Cardiac Output and Stroke Volume in PE
“Study device no longer available”
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.