Determination of SpO2 differences between different SpO2 sensors, approved for monitoring of premature and newborn infants

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00027285

Enrollment

Registered

2021-11-25

Start date

2021-10-14

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

Clinical monitoring (SpO2)

Interventions

Group 1: Simultaneous SpO2 measurement with 3 different sensors (LNCS, RD & PPG) on 3 different extremities. Rotation of the sensors every 2h (during meal) with a total measuring time of 6h.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: - Premature infants 0.21 (combinations possible)) - Echocardiographically excluded open ductus arteriosus botalli with bi-directional or right-left shunt.

Exclusion criteria

Exclusion criteria: - Palliative care situation - Less than 12 meals a day

Design outcomes

Primary

Measure	Time frame
Average percentage deviation of the determined SpO2 values ??between LNCS sensors and PPG or RD sensors	—

Secondary

Measure	Time frame
- Mean deviation in the SpO2 ranges 95%. -% time in target (SpO2 90-95%),% time above target,% time below target, -% time with hypoxemia (SpO2 97%)	—

Countries

Germany

Contacts

Public ContactChristian A. Maiwald

Abteilung für Neonatologie

christian.maiwald@med.uni-tuebingen.de07071 29 81418

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 7, 2026