Scientists hunt for brain injury fingerprints in blood and spit
NCT ID NCT01171131
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study looked for protein markers in the blood and saliva of 96 people with long-term traumatic brain injury (TBI). Researchers compared samples from blast injury and non-penetrating injury patients to find common changes. The goal is to better understand the lasting effects of head trauma and identify new targets for treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could point toward new targets for treating long-term effects of traumatic brain injury.
- What could go wrong
- This is a small pilot study (96 people) that only looks for markers, not a treatment. The findings may not lead to any new therapies.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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96 people
The number who actually took part.
- Started
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Apr 2010
- Finished
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Mar 2016
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
TIRR Clinics
- Ages
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18 to 70 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Chronic TBI patients: Inclusion Criteria Have a history of head trauma manifesting in one or more of the following: * Loss of consciousness * Post-traumatic amnesia * Focal neurologic deficits, seizure * Persistent symptoms of increased arousal (e.g. difficulty falling or staying asleep, anger and hypervigilance) * Impairment in social, occupational, or other important areas of functioning (e.g. problems with work and relationships.) Exclusion Criteria Inability to obtain informed consent and if they are non-communicative (i.e. in a vegetative state). Healthy volunteers: Inclusion Criteria * No significant medical history * Take no medications (other than birth control pills) * Fever free * No history of head trauma or recent injury/infection * No history of neurological or psychiatric disorders or alcohol or drug dependency. Exclusion Criteria * Inability to provide informed consent * age/gender match not available in TBI cohort
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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TIRR
Houston, Texas, 77030, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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