The clinical trial of portable capnometer for mechanically ventilated preterm infants immediately after birth

The clinical trial of portable capnometer for mechanically ventilated preterm infants immediately after birth - The clinical trial of portable capnometer for mechanically ventilated preterm infants immediately after birth

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000040569

Enrollment

Registered

2020-05-29

Start date

2019-04-01

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Preterm infants

Interventions

Monitoring with portable end-tidal carbon dioxide monitor

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Infants born at Osaka Women's and Children's Hospital and from 26 to 32 weeks' gestation and intubated at resuscitation room or delivery room from 1st of April 2019 to 30th of September 2020 (extend as needed)

Exclusion criteria

Exclusion criteria: Infants with congenital anomalies that significantly affect their respiratory or circulatory status

Design outcomes

Primary

Measure	Time frame
Either partial pressure of arterial carbon dioxide on admission in neonatal intensive care unit or that of two hours after birth	—

Secondary

Measure	Time frame
Longitudinal development and complications	—

Countries

Japan

Contacts

Public ContactMasahi Hotta

Osaka Women's and Children's Hospital Department of Neonatal Medicine

spyf88d9@yahoo.co.jp0725-56-1220

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026