Houston, TXNCT06828107Now EnrollingIRB Ready

Traumatic Brain Injury Clinical Trial in Houston, TX

Access cutting-edge traumatic brain injury treatment through this clinical trial at a research site in Houston. Study-provided care at no cost to qualified participants.

Sponsored by Sense Diagnostics, LLC

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Expert Care in Houston

Access traumatic brain injury specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related traumatic brain injury treatment provided free

Apply for This Houston Location

Check if you qualify for this traumatic brain injury clinical trial in Houston, TX

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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 Houston

    Convenient for TX 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 Houston site if eligible
  4. 4Begin participation

About This Traumatic Brain Injury Study in Houston

The study population will consist of 3 mutually-exclusive sets of patients and subjects: * TBI patients with intracranial bleeding * TBI patients without intracranial bleeding * Control subjects with normal brain health. Research subjects ages 22 and older will be enrolled. All TBI patients must be monitored with the SENSE Device within 6 hours of a diagnostic head CT scan ordered by a treating clinician and within 24 hours of injury.

Sponsor: Sense Diagnostics, LLC

Who Can Participate

Inclusion Criteria

• Male or female adults age 22 and older
Patients with TBI who have a head CT scan obtained in the mobile stroke unit, emergency department, or hospital, ordered by a treating clinician OR control subjects with normal brain health.
For patients with traumatic intracranial hemorrhage, blood is visible on ≥ 3 consecutive axial CT slices.
Signed written informed consent by study subject or, if subject is unable, by subject's next of kin or legally authorized representative.
Willingness and ability to comply with schedule for study procedures.

Exclusion Criteria

• Female patients who are pregnant or lactating.
SENSE Device is unable to be placed within 6 hours of a standard of care head CT and within 24 hours of injury.
Open skull fracture (closed skull fracture is not an exclusion).
Metallic intracranial clip, coil, or device (such as metallic ICP monitor).
Presence or history of any other condition or finding that, in the investigator's opinion, makes the patient unsuitable as a candidate for the SENSE Device monitoring or study participation or may confound the outcome of the study.
Planned placement of an intraventricular catheter prior to study enrollment.
Planned intracranial surgery prior to study enrollment.
Current participation in a medical or surgical interventional clinical trial.
Use of continuous EEG monitoring at the time of enrollment.
Clinical uncertainty about the presence or absence of hemorrhage on the enrolling head CT.
Control subjects with normal brain health will have no known history of seizure, stroke, brain tumor, TBI requiring emergency room evaluation, concussion within the previous 6 months, hydrocephalus, intracranial vascular malformation, other structural brain disease, or intracranial surgery. Benign headache disorders (e.g. migraine headache, tension headache), and mild concussion \> 6 months prior to enrollment are not exclusions.

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 Houston?

Yes, this clinical trial (NCT06828107) has an active research site in Houston, TX 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.

Traumatic Brain Injury Treatment Options in Houston, TX

If you're searching for traumatic brain injury treatment options in Houston, TX, this clinical trial (NCT06828107) 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 Houston research site is actively enrolling participants for this clinical trial. You'll receive care from experienced traumatic brain injury 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 traumatic brain injury clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Houston, TX