Autopsy report · NCT02484287
Quality Control: A Prospective Analysis of EVD Effectiveness
Cause of deathStaffing, sites or logistics
“PI left institution prior to study completion”
Life of this trial
- Registered 10 months before it started.
- Ran for about 2 years 3 months before it stopped.
- 60 participants enrolled.
- Results were posted on the registry 5 years after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- University of Oklahoma
- Sponsor type
- University, hospital or other
- Conditions
- Catheter Related Infections
- Interventions
- The Integra External Drainage Catheter.; The Ventriclear EVD Antibiotic Catheter; The Codman Bactiseal EVD Catheter Set
- Participants
- 60
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Fabrication of Naso-alveolar Molding (NAM) Appliance in Cleft Lip and Palate (CLP) From Digital Magnetic Resonance Imaging (MRI) Face Scan
“PI left institution” - Determining if the Buzzy® Personal Pain Relief Device Reduces Injection Pain of Propofol as Much as Intravenous Lidocaine in Children
“PI left institution and study activity was not continued (enrollment not complete)” - Oscillatory Versus Non-Oscillatory Nasal Continuous Airway Pressure Neonatal Respiratory Support
“PI has left Institution” - RCT of SPG Blocks for Post-dural Headache
“Both Study PI's left the institution”
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.