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Clinical Trial Summary

The objective of the SafeBoosC-IIIv trial is to evaluate cerebral oximetry added to usual care versus usual care in mechanically ventilated newborns. The hypothesis is that the intervention will decrease a composite outcome of death or moderate to severe neurodevelopmental disability and/or increase the mean PARCA-R non-verbal cognitive score at two years of corrected age.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05907317
Study type Interventional
Source Copenhagen Trial Unit, Center for Clinical Intervention Research
Contact
Status Not yet recruiting
Phase Phase 3
Start date February 1, 2024
Completion date February 1, 2029

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