Prospective evaluation of the non-invasive ICP Headsense monitor in TBI patients undergoing invasive ICP monitoring

Completed

• Conditions: neurotrauma; 10021666

• Registration Number: NL-OMON41180
• Lead Sponsor: Sint Elisabeth Ziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 15

Inclusion Criteria

severe traumatic brain injury, age18-85 years, ICU admitted, invasive ICP monitor

Exclusion Criteria

ear infection, pregnancy

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Demonstrate the HS-1000 performance and accuracy in ICP monitoring </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>ergonomics and functionality</p><br>