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Clinical Trial Summary

The goal of this clinical trial is to test a modified smart soft contact lens in neonates and infants at risk of developing hydrocephalus. The main questions it aims to answer are: - Can the device distinguish between intracranial pressure variations in neonates and infants diagnosed with hydrocephalus and those without - Can the device compare pressure dynamics between pre- and post-operative periods in neonates and infants who undergo surgical treatments Participants will undergo standard of care evaluations for hydrocephalus (anterior fontanelle assessment and head circumference measurement) and wear the device during standard of care evaluation; pre- and post- ventricular reservoir taps, as applicable; and/or pre- and post-operatively, as applicable.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06310213
Study type Interventional
Source Indiana University
Contact Clinical Research Coordinator
Phone 317-944-6201
Email mkillin@iu.edu
Status Not yet recruiting
Phase N/A
Start date April 1, 2024
Completion date July 1, 2028

See also
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