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NCT06637917

Pulse Oximetry Performance Comparison in Newborns

Completed Last updated 12 March 2026
What this trial tests

trial testing OxySoftN™ Neonatal-Adult SpO2 Sensor with N600X Nellcor™ Patient Monitoring System in Newborn in 120 participants. Completed in 18 September 2025.

Timeline
10 September 2024
Primary endpoint
18 September 2025
18 September 2025

Quick facts

Lead sponsorMedtronic - MITG
StatusCompleted
Study typeOBSERVATIONAL
Enrollment120
Start date10 September 2024
Primary completion18 September 2025
Estimated completion18 September 2025
Sites3 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Medtronic - MITG — full company profile →

Who can join

29 Weeks and older, any sex, with Newborn or Birth, Preterm. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The overall purpose is to directly compare pulse rate (PR) acquisition and oxygen saturation performance between two pulse oximeters (PO) in newborns.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Newborn

Currently open trials in the same condition.

Other Medtronic - MITG trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06637917.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing