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NOT YET RECRUITING
NCT07060911
NA
Pivotal Study to Assess Safety and Performance of Neola®, a Novel Lung Monitoring Device for Neonates
Sponsor: Neola Medical Inc
View on ClinicalTrials.gov
Summary
Pivotal study to assess safety and performance of Neola®, a novel lung monitoring device for neonates
Key Details
Gender
All
Age Range
1 Day - 44 Weeks
Study Type
INTERVENTIONAL
Enrollment
22
Start Date
2026-03
Completion Date
2027-02
Last Updated
2025-07-11
Healthy Volunteers
No
Interventions
DEVICE
Lung monitoring with the Neola device
Lung monitoring with the Neola device
Locations (2)
Stanford Lucile Packard Children's Hospital Neonatal Intensive Care Unit
Palo Alto, California, United States
Cooper Health System
Camden, New Jersey, United States