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Clinical Trial Summary

This study evaluates the performance of a thermal anisotropy measurement device for non-invasively assessing CSF shunt flow. Patients with an existing implanted shunt and symptoms of shunt malfunction who require shunt revision surgery will be evaluated with the study device to assess flow in CSF shunts as confirmed by surgical outcomes at 7 days. If successful, this study will show that the study device accurately distinguishes between functioning (flowing) and non-functioning (non-flowing) shunts.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06409286
Study type Observational
Source Rhaeos, Inc.
Contact Anna Lisa Somera
Phone 855-814-3569
Email info@rhaeos.com
Status Not yet recruiting
Phase
Start date May 2024
Completion date December 2024

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