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NCT07346976: ETCO

Investigation Into the Dynamic Variations of End-Tidal Carbon Monoxide Concentration (ETCOc) in Neonates Utilizing Non-Dispersive Infrared Spectroscopy and Its Implications for Jaundice Management

Recruiting now NA Last updated 16 January 2026
What this trial tests

NA trial testing Erythrocyte Life Span Tester in Neonatal Hyperbilirubinemia in 100 participants. Currently enrolling.

Timeline
5 December 2025
Primary endpoint
1 July 2026
1 July 2027

Quick facts

Lead sponsorThe Fourth Affiliated Hospital of Zhejiang University School of Medicine
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeother
Enrollment100
Start date5 December 2025
Primary completion1 July 2026
Estimated completion1 July 2027
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

The Fourth Affiliated Hospital of Zhejiang University School of Medicine

Who can join

Adults 0 Days to 28 Days, any sex, with Neonatal Hyperbilirubinemia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of this study is to ascertain the diagnostic threshold of end-tidal carbon monoxide (ETCOc, adjusted for ambient CO levels) within the first three days postpartum, stratified by neonatal age at birth. Additionally, the study aims to evaluate the concordance of the risk range of ETCOc, as measured by non-dispersive infrared spectroscopy, with existing literature, and to assess the reliability of this technology in the management of neonatal hyperbilirubinemia.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Neonatal Hyperbilirubinemia

Currently open trials in the same condition.

Other The Fourth Affiliated Hospital of Zhejiang University School of Medicine trials

Trials by the same sponsor.

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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/NCT07346976.

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