Stroke Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You are male or female (by birth) and are 18 years old or older at the time of joining the trial.
- You are already receiving continuous brain pressure monitoring through an invasive device (such as a bolt or drain) as part of your normal medical care.
- The brain pressure monitoring device goes into the brain tissue or the fluid-filled spaces of the brain.
- You are already receiving continuous blood pressure monitoring through an invasive device as part of your normal medical care.
Who may not be able to join:
- You have any implant (for cosmetic or other reasons) in the forehead bone that is close enough to potentially touch the study's sensor device.
- You have open wounds on your forehead that would prevent the study's sensor from being safely placed on unbroken skin.
- Scans taken when you were admitted to hospital show that the skull at the area where the sensor would be placed is not fully intact.
- You are taking part in another study or receiving a treatment that could interfere with your standard brain pressure monitoring or with the study's sensor device.
- Your skull has had a section surgically removed, unless the study's sensor can be placed on a part of the skull that is still intact.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Ramani Balu, MD, PhD, Inova Fairfax Hospital
Phone: 305-290-1680
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
A test of the difference in estimation errors between two non-invasive ICP estimation models: one trained with ABP and CoMind One EFS CBFi, and one trained only using ABP; Models trained using CoMind CBFi and ABP will be evaluated based on their limits of agreement (LOA) with invasive ICP.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 5 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.