CompletedNCT02612207
Point-of-Care System for Determination of Bilirubin Capacity in Neonates
Studying Chronic bilirubin encephalopathy
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Stanford University
- Principal Investigator
- Vinod K Bhutani, MDPI
- Intervention
- Bilirubin Binding Capacity by Hematofluorometry Validation(device)
- Enrollment
- 161 enrolled
- Eligibility
- All sexes
- Timeline
- 2015 – 2018
Study locations (2)
- Lucile-Packard Children's Hospital at Stanford, Stanford, California, United States
- AVIV Biomedical, Inc., Lakewood, New Jersey, United States
Collaborators
Aviv Biomedical, Inc.
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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