Optical Detection Infiltration/Extravasation in Neonates (ODINE) (ODINE)
Extravasation Injury, Infant, Premature, Diseases
About this trial
This is an interventional prevention trial for Extravasation Injury
Eligibility Criteria
Inclusion Criteria: Term and pre-term infants; birth weight > 1.5 kg; need for continuous IV therapy with an expected duration > 24 hours. Exclusion Criteria: birth weight </= 1.5 kg; non continuous IV therapy; IV therapy expected duration </= 24 hours; skin disorders.
Sites / Locations
- FPGemelliIRCCS
Arms of the Study
Arm 1
Experimental
Sensor Group
The first half sample size Peripheral intravenous canula will be enrolled in a non-alarming group. ivWatch will monitor the Peripheral intravenous canula insertion site collecting data without notifications. The goals of the study on the nonalarming group are: a) to evaluate ivWatch sensitivity to detect infiltration in comparison with nurse standard of care; b) to estimate the difference in terms of time to detection of ivWatch in comparison with nurse standard of care