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Optimal target range of closed loop inspired oxygen support in preterm infants

Optimal target range of closed loop inspired oxygen support in preterm infants - OPTICLIO study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON38580
Enrollment
41
Registered
2013-09-12
Start date
2014-01-18
Completion date
Unknown
Last updated
2024-04-23

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

Conditions

Hypoxie en hyperoxie bij prematuriteit Neonatal hypoxie and hyperoxia

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
2 Years to 11 Years

Inclusion criteria

Inclusion criteria: Born with a gestational age between 24-32 weeks Birth weight between 0.4 and 2 kg Recieving NCPAP or NIPPV with supplemental oxygen for more than 18 hours per day

Exclusion criteria

Exclusion criteria: Lack of parenteral informed consent Congenital malformation Requiring vasopressors 48 hours before enrollment Culture proven infection 72 hours before enrollment

Design outcomes

Primary

MeasureTime frame
The main outcome parameter will be the proportion of time spent within the saturation ranges used in clinical setting, being 86-94%.

Secondary

MeasureTime frame
Secondary outcomes will be the proportion of time being in hypoxia or hyperoxemia, the distribution of SpO2 between the different periods, and the duration of episodes with hypoxia or hyperoxemia.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)