Brain Trauma

5

Review clinical trials related to Brain Trauma. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

BRIDGE-US: Bridging Readiness in Deployed Neurotrauma Gaps for Excellence

The purpose of this research study is to prospectively collect biospecimens, imaging, and clinical data from patients with penetrating brain injuries across high-volume PBI sites in the US (including UChicago). Biospecimens will undergo biomarker analysis - biomarker data specific to PBI is extremely limited, and could provide critical insight to outcome identification and clinical decision making. This data will be used to build the first comprehensive PBI Data Commons, biorepository, and imaging repository which will create the infrastructure necessary to close critical knowledge gaps, advance biomarker discovery specific to PBI, and provide the foundation for future research aimed at improving prognostication and treatment for patients with this devastating injury.

Participants needed: 270
Trial details
Age: 16+Biological sex: AllType: ObservationalSponsor: University of ChicagoUpdated: Jun 9, 2026Locations: 1Duration: 7 Days
Eligibility criteria

Age: Subjects aged 16 years and older [+2]

Dead on Arrival (DOA): Patients who receive CPR with no return of pulse [+4]

Status: Recruiting

Remotely Supervised tDCS+ for Complex Attention in mTBI (Cognetric)

The proposed study will evaluate a new approach to cognitive rehabilitation of mTBI using a brain stimulation technique called "Remotely Supervised Transcranial Direct Current Stimulation combined with Cognitive Training" (RS-tDCS+) which has shown promise for improving complex attention in both healthy and clinical populations. RS-tDCS+ is a home-based, low-risk, non-invasive technique that is designed to boost cognitive training by enhancing learning and the brain's ability to reorganize connections. This study will evaluate RS-tDCS+ for improving complex attention in Active Duty Service Members (ADSM) and Veterans with a history of mTBI. Different tests of complex attention and symptom questionnaires will be used to determine the effects of real versus sham (placebo) RS-tDCS+. Second, the investigators will investigate electrical and connectivity changes in the brain associated with RS-tDCS+ using electroencephalogram (EEG) and magnetic resonance imaging (MRI). Third, the investigators will investigate the lasting effects of any observed changes by evaluating participants at 1 and 6 weeks post-treatment. Lastly, the investigators will explore the impact of individual differences (e.g., PTSD, depression, sleep quality, time since injury, baseline impairment, age, sex, ADSM versus Veteran) on treatment outcome.

Participants needed: 160
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: United States Naval Medical Center, San DiegoUpdated: Nov 12, 2025Locations: 2
Eligibility criteria

Active-Duty Service Members. [+6]

Presence of a medical, psychiatric, physical or non-physical disease, disorder,... [+8]

Status: Recruiting

Biofeedback for Hemianopia Vision Rehabilitation

Patients with brain injury secondary to stroke, surgery, or trauma frequently suffer from homonymous hemianopia, defined as vision loss in one hemifield secondary to retro- chiasmal lesion. Classic and effective saccadic compensatory training therapies are current aim to reorganize the control of visual information processing and eye movements or, in other words, to induce or improve oculomotor adaptation to visual field loss. Patients learn to intentionally shift their eyes and, thus, their visual field border, into the area corresponding to their blind visual field. This shift brings the visual information from the blind hemifield into the seeing hemifield for further processing. Patients learn, therefore, to efficiently use their eyes "to keep the 'blind side' in sight". Biofeedback training (BT) is the latest and newest technique for oculomotor control training in cases with low vision when using available modules in the new microperimetry instruments. Studies in the literature highlighted positive benefits from using BT in a variety of central vision loss, nystagmus cases, and others.The purpose of this study is to assess systematically the impact of BT in a series of cases with hemianopia and formulate guidelines for further use of this intervention in vision rehabilitation of hemianopia cases in general.

Participants needed: 32
Trial details
Age: 18-90Biological sex: AllType: InterventionalSponsor: University Health Network, TorontoUpdated: May 9, 2025Locations: 1
Eligibility criteria

hemianopia cases previously diagnosed accordingly by microperimetry and other te... [+2]

previous or current treatment for low vision rehabilitation [+4]

Status: Not yet recruiting

Characterization of the Sleep-Wake Cycle in Traumatic Brain Injury Patients with a Disorder of Consciousness

Each year in France, 160,000 peoples suffer from a mild or severe traumatic brain injury (TBI). Sleep plays a crucial role in the process of brain plasticity, which is essential for neurological and cognitive recovery. However, the sleep-wake cycle is rarely, if ever, evaluated in patients with TBI and consciousness disorders within Post-Resuscitation Rehabilitation Units (SRPR). Caregivers develop, on a daily basis, an intuitive understanding of the patient's overall condition. This expertise deserves to be validated using objective sleep assessment tools (actigraphy). If proven accurate, it could lead to the implementation of a sleep-wake cycle evaluation protocol within SRPRs.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Hospices Civils de LyonUpdated: Jan 9, 2025Locations: 1
Eligibility criteria

Admission to the Post-Resuscitation Rehabilitation Unit or the Neurological Inte... [+5]

Admission for status epilepticus [+3]

Status: Not yet recruiting

VisAR Augmented Reality Navigation of Ventriculostomy

This study is intended to evaluate the feasibility of using VisAR augmented reality surgical navigation during placement of an external ventricular drain (EVD). The investigators are interested in confirming the design of the VisAR headset is compatible with this bedside procedure.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Dartmouth-Hitchcock Medical CenterUpdated: Aug 7, 2024
Eligibility criteria

Adult patients, 18 years and older, determined to need an external ventricular d...

Patients less than 18 years of age. [+2]