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Assessment of CSF Shunt Flow With Thermal Measurements A

NCT05015751 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 44

Last updated 2024-12-19

Study results available
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Summary

This study evaluates the performance of a non-invasive thermal measurement device for assessing CSF shunt flow. Patients with an existing implanted shunt and symptoms of shunt malfunction will be evaluated with the study device.

Conditions

  • Hydrocephalus

Interventions

DEVICE

Thermal Anisotropy Measurement Device

A wireless device for non-invasively assessing CSF shunt flow.

Sponsors & Collaborators

  • Rhaeos, Inc.

    lead INDUSTRY

Principal Investigators

  • Sandi Lam · Ann & Robert H Lurie Children's Hospital of Chicago

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-08-25
Primary Completion
2022-07-13
Completion
2022-07-13
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05015751 on ClinicalTrials.gov