Paid Traumatic Brain Injury Clinical Trials in Tampa, FL – Now Enrolling
Traumatic brain injuries (TBI) range from mild concussions to severe trauma. Santos Research Center in Tampa is now enrolling participants for a clinical trial. Qualified individuals may receive study-related care at no cost and be compensated for time and travel.
Now Enrolling – Traumatic Brain Injury Clinical Trial
Traumatic brain injury (TBI) affects millions of people each year and may impact cognitive function, emotional health, and quality of life. Symptoms can range from dizziness and fatigue to altered consciousness, memory issues, or difficulty concentrating.
In some cases, TBI may lead to complications such as intracerebral hemorrhage, cerebral edema, or encephalopathy. Ongoing research seeks to better understand brain recovery, evaluate potential therapies, and improve long-term outcomes.
Areas of study may include:
- » Biomarkers such as glial fibrillary acidic protein (GFAP)
- » Neuroimaging and intracranial pressure monitoring
- » Management of post-TBI depression, fatigue, and pain
- » Predictive tools using machine learning and cohort data
Disclaimer: The information in this section is provided for general educational purposes only. Specific details about the TBI clinical trial at Santos Research Center will be reviewed during the informed consent process.
Traumatic Brain Injury
A mild traumatic brain injury (TBI) can temporarily affect brain neurons, while more severe ones can cause complicated long-term physical damage to the brain.
A TBI can have wide-ranging physical and psychological effects. Some symptoms may appear right after the traumatic event, while others may appear days or weeks later.
Details
- Start Date: August 2021
- Phase: Phase 2
- Study Type: Interventional
- Insurance: No insurance is needed
- Benefits: Compensation up to $2,000 for time and travel
Eligibility
- From 18 to 75 years of age
- History confirmed by evidence from medical information
- Must have had no further head trauma in the last 6 months
- Must have TBI
Excluding
- Progressive dementia
- Penetrating head trauma
- Significant symptoms of a depressive disorder
- Significant ongoing psychiatric or substance abuse problems
- Clinically significant or unstable systemic disease
Why Join a TBI Clinical Trial?
Clinical trials are vital to improving patient outcomes and shaping the future of neuroscience and intensive care medicine.
By joining, you contribute to:
- » Developing new therapies and brain recovery protocols
- » Advancing research in ICU monitoring, intracranial pressure, and oxygen therapy
- » Understanding post-TBI symptoms like depression, headache, or fatigue
- » Informing national research programs like TRACK-TBI or DECRA
All clinical trials adhere to safety guidelines established by the Food and Drug Administration (FDA) and reviewed by institutional review boards (IRBs). Every protocol is explained in full detail during the consent process to ensure you’re comfortable with your participation.
What to Expect
Participating in a clinical trial can feel unfamiliar, especially if it’s your first time. At Santos Research Center, the team is committed to making the process clear, supportive, and respectful from start to finish.
Here’s a step-by-step look at what you can typically expect when you join a TBI clinical study.
Pre-Screening Call
A coordinator will discuss your medical history and check your initial eligibility.
Clinic Visit
You’ll meet with a physician, review the informed consent, and complete exams related to cognition, blood tests, or neuroimaging.
Treatment & Monitoring
If eligible, you may receive investigational medication or therapies. Throughout the trial, clinicians monitor your progress, response to treatment, and any side effects.
The steps described here are typical in many clinical trials but may vary. Your participation will follow the specific protocol reviewed with you during the consent process.
Why Patients Trust Santos Research Center
Patients across Central Florida choose Santos Research Center, Corp. for more than just access to clinical trials—they choose us for trust, transparency, and compassionate care rooted in clinical excellence.
Join a TBI Clinical Trial in Tampa Today
Help advance brain health and recovery through TBI clinical research. By joining a traumatic brain injury study, you support medical science while accessing no-cost, study-related care. Compensation for time and travel may be available. Participation is always voluntary.
Why Participants Choose Us:
- » 400+ Clinical Studies Completed: A strong track record in advancing research across neurology, infectious disease, and more.
- » IRB & FDA-Compliant: Every study follows strict ethical and safety standards approved by regulatory bodies.
- » Bilingual Staff: Spanish and English-speaking team members ensure clear communication for all patients.
- » Convenient Tampa Location: Easy access, free parking, and flexible scheduling make participation simple.
- » Trusted by the Community: Patients praise our professionalism, clean facilities, and caring staff. Your comfort and safety are always our top priorities.
Also Enrolling at Santos Research Center
What Participants Say About Santos Research Center
Patients trust Santos Research Center for our compassionate care, professional staff, and clean, welcoming environment.
These testimonials reflect our ongoing commitment to putting patient safety, comfort, and quality of care first.
Frequently Asked Questions
The following answers provide general information about traumatic brain injury (TBI) clinical trials and current medical research. Specific eligibility, procedures, and risks vary by study and are fully explained during the informed consent process.
What are the new treatments for TBI?
New studies are testing medications, personalized therapies, and noninvasive techniques like neuromodulation. Some clinical trials explore drug efficacy, pain management, and ways to improve cognition, inflammation, and quality of life after brain injury.
What is the average life expectancy after a TBI?
It depends on factors like injury severity, medical care received in the emergency department or intensive care unit, and underlying health conditions. Researchers are using cohort studies, biomarkers, and clinical data to better understand survival rates and long-term outcomes.
Can someone fully recover from a severe traumatic brain injury?
Some people make a full recovery, while others may face chronic symptoms such as fatigue, stress, confusion, or impaired consciousness. Clinical research helps clinicians and physicians improve treatment plans and long-term management strategies.
What are biomarkers and why do they matter in brain injury studies?
Biomarkers, such as glial fibrillary acidic protein (GFAP), are measurable substances in the blood or cerebrospinal fluid that help detect, monitor, or predict outcomes after a brain injury. They are key to early diagnosis, especially in ICU or hospital settings.
Will I be compensated for participating?
Many clinical trials, including this one, offer compensation for time, travel, and study-related visits. The amount may vary based on the study’s design, procedures, and duration.
What are the DECRA and TRACK-TBI trials?
These are large national clinical trials funded by organizations like the National Institutes of Health. They use observational and randomized data to evaluate treatments like decompressive craniectomy, transcranial Doppler, and intracranial pressure monitoring in TBI patients.
Is participating in a clinical trial safe?
Yes. All medical studies follow guidelines set by the Food and Drug Administration (FDA) and are reviewed by an Institutional Review Board (IRB). These protections help reduce risk and ensure ethical standards in emergency medicine, neurology, and intensive care research.
Can I leave the study after enrolling?
Yes. Your participation is voluntary. You can withdraw at any time, for any reason, without affecting your access to health care or support services.
How is my personal health information protected?
All clinical trial data is handled in compliance with HIPAA policies and stored securely. Studies use strict protocols to protect patient privacy, especially when collecting data from labs, questionnaires, blood samples, or imaging during the study.
Glossary
Acute Phase:
The early stage right after an injury or when symptoms first appear. In TBI, this is when doctors begin urgent care.
Biomarker:
A measurable substance in the body (like a protein in your blood) that can help doctors detect or track a disease or injury.
Cerebral Edema:
Swelling in the brain caused by a buildup of fluid, which can occur after a traumatic brain injury.
Clinical Trial:
A medical study that tests how safe and effective a treatment, drug, or therapy is in people. Participation is always voluntary.
Cognition:
The brain’s ability to think, remember, focus, and make decisions. TBI can affect cognition in different ways.
Cohort Study:
A type of research where a group of people (a "cohort") is followed over time to observe health outcomes.
Encephalopathy:
A general term for changes in brain function that can cause confusion, memory loss, or problems thinking clearly.
Glial Fibrillary Acidic Protein (GFAP):
A protein found in the brain that can be measured in blood after a TBI. It’s a type of biomarker.
Institutional Review Board (IRB):
A group that reviews and approves clinical trials to make sure they are ethical and protect participants’ safety.
Intracerebral Hemorrhage:
Bleeding inside the brain, which can happen after a serious head injury.
Intracranial Pressure Monitoring:
A way to measure the pressure inside the skull, often used in patients with severe TBI.
Observational Study:
A research study where doctors observe what happens over time without giving a new treatment.
TRACK-TBI / DECRA:
Major national studies that collect data from TBI patients to better understand how injuries are treated and how patients recover.