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

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

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON41180

Enrollment

Registered

2014-06-18

Start date

2014-07-01

Completion date

Unknown

Last updated

2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

neurotrauma

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

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

Exclusion criteria

Exclusion criteria: ear infection, pregnancy

Design outcomes

Primary

Measure	Time frame
Demonstrate the HS-1000 performance and accuracy in ICP monitoring	—

Secondary

Measure	Time frame
ergonomics and functionality	—

Countries

Netherlands

Outcome results