None listed
Conditions
Brief summary
To try to develop a less risky method for measuring brain fluid pressure.
Interventions
Subjects who have invasive intracranial pressure monitors in place will have recordings of central retinal vein pulsation pressure by ophthalmodynomometry 4 times over 24 hours.
Sponsors
Sir Charles gairdner Hospital
Study design
Allocation
Non-randomised trial
Primary purpose
Diagnosis
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Healthy volunteers
No
Inclusion criteria
subjects who have intracranial pressure monitors in place who are conscious and able to provide informed consent.
Exclusion criteria
subjects who cannot sit up. subjects who cannot tolerate mydriatic eye drops.
Outcome results
None listed