Washington Dc, DCNCT06368648Now EnrollingIRB Ready

Intracranial Pressure Clinical Trial in Washington Dc, DC

Access cutting-edge intracranial pressure treatment through this clinical trial at a research site in Washington Dc. Study-provided care at no cost to qualified participants.

Sponsored by CoMind Technologies Limited

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Expert Care in Washington Dc

Access intracranial pressure specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related intracranial pressure treatment provided free

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Check if you qualify for this intracranial pressure clinical trial in Washington Dc, DC

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Washington Dc

    Convenient for DC residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Washington Dc site if eligible
  4. 4Begin participation

About This Intracranial Pressure Study in Washington Dc

The purpose of this research, which has been determined as non-significant risk by the central IRB overseeing the study, is to obtain information to help further develop a machine (a medical device) to measure the pressure around the brain from the outside (this pressure is called intracranial pressure or ICP). Monitoring and managing ICP is an important part of care for patients with conditions such as Traumatic Brain Injury (TBI). However, the current way of measuring ICP requires surgery to drill a hole into the skull, and therefore can introduce additional risks such as infections and pain. Recent research has shown it may be possible to measure ICP without needing surgery. This technology is in development, but large amounts of data is required to build these new devices. Through collecting a large database of information from patients who have both the routine surgical device and the research device applied to their head, the research team will work to develop and test an effective and potentially safer way of monitoring patient ICP.

Sponsor: CoMind Technologies Limited

Who Can Participate

Inclusion Criteria

Male or female sex at birth, and aged 18 years or older on the date of enrollment.
Receiving continuous invasive ICP monitoring (Bolt or EVD) as part of standard care.
Invasive ICP monitor catheter penetrating the parenchyma or ventricles.
Receiving continuous invasive ABP monitoring as part of standard care.

Exclusion Criteria

Presence of any implant (cosmetic or otherwise) in the frontal bone in such proximity to the CoMind One EFS Sensor that they might physically touch.
Open wounds on the forehead such that CoMind One EFS Sensor cannot be safely placed over an area of intact skin
Presenting with radiographic evidence of a non-intact skull at the recording site on admission.
If patient is enrolled in an intervention/study that may interfere with SoC ICP measurements or the CoMind One EFS device measurement then the patient is ineligible.
Patients with decompressive craniectomy will be excluded unless a CoMind One EFS recording can be made from intact skull.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Washington Dc?

Yes, this clinical trial (NCT06368648) has an active research site in Washington Dc, DC that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Intracranial Pressure Treatment Options in Washington Dc, DC

If you're searching for intracranial pressure treatment options in Washington Dc, DC, this clinical trial (NCT06368648) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Washington Dc research site is actively enrolling participants for this clinical trial. You'll receive care from experienced intracranial pressure specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all intracranial pressure clinical trials near you to find additional studies recruiting in your area.

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