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Clinical Trial Summary

Implementing target ranges for regional cerebral saturations in extremely preterm infants in the first week of life may improve neurodevelopmental outcomes at 22-26 months corrected age compared to those without targeted cerebral saturations (Csat) using near-infrared spectroscopy (NIRS). Infants will be randomized to a targeted cerebral saturation monitoring group with visible reading of Csat or to a control group with cerebral saturation monitoring, but with blinded Csat measures. Those in the targeted Csat group will follow a treatment guideline to maintain cerebral oxygenation in the target range. The primary outcome is neurodevelopmental outcome as determined by Bayley III cognitive scale score.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04439968
Study type Interventional
Source Stanford University
Contact
Status Active, not recruiting
Phase N/A
Start date August 10, 2021
Completion date December 31, 2025

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