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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