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Clinical Trial of Noninvasive Intracranial Pressure Measurement

Clinical Trial of Noninvasive Intracranial Pressure Measurement

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs032200074
Enrollment
60
Registered
2020-07-29
Start date
2020-07-29
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

disease in neurosurgical field

Interventions

External auditory canal pressure is recorded by the original headset placed on the external auditory canal.

Sponsors

Goto Tetsuya
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. patient who have a disease in neurosurgical field 2. age: over 1 year 3. sex: not concern 4. informed consent from patient him/herself or legal representative when the patient is under 20 years or loss of consciousness. 5. patient of increased ICP state 6. patient of intact middle and external auditory canal 7. patient who had a radiological examination just before examination 8. patient who can keep resting state over 30 minutes. 9. patient who is safe against occlusion of a ventricular drainage over 30 minutes.

Exclusion criteria

Exclusion criteria: 1. past history: ottitis 2. past history: pyramidal bone fracture 3. severe facial and head laceration 4. patient who is considered to be inappropriate for inclusion to this research

Design outcomes

Primary

MeasureTime frame
This research is for the refinement of the analogical program in the non-invasive intracranial pressure apparatus.

Secondary

MeasureTime frame
not arranged.

Contacts

Public ContactTetsuya Goto

St.Marianna University School of Medicine Hospital

tegotou@marianna-u.ac.jp+81-44-977-8111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026