Umbilical cord oximetry for measuring heart rate in neonatates at birth: a feasibility study

Umbilical cord oximetry for measuring heart rate in neonatates at birth: a feasibility study - U-COUNT study

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON49437

Enrollment

Registered

2020-01-21

Start date

2020-01-31

Completion date

Unknown

Last updated

2024-04-15

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

Conditions

neonatal changes from intrauterine to extrauterine life neonatal transition

Interventions

None listed

Eligibility

Age

2 Years to 11 Years

Inclusion criteria

Inclusion criteria: Infants born between 26-42 weeks gestational age where stabilisation at birth is anticipated.

Exclusion criteria

Exclusion criteria: Infants participating in the ABC3 trial, who are randomized to physiological based cord clamping and are stabilised on the Concord resuscitation table.

Design outcomes

Primary

Measure	Time frame
The time needed to obtain an accurate HR signal after sensor placement. An accurate signal will be defined as a stable display of HR with a good plethysmograph signal, without low signal alarms.	—

Secondary

Measure	Time frame
* Proportion of infants in whom the PO sensor can successfully be placed on the umbilical cord. * Proportion of infants with an accurate HR signal. * HR (umbilical and right hand ) at 2 second intervals during the first 10 min after birth.	—

Countries

Netherlands

Outcome results