An interventional study of MRI in Concussion and Traumatic Brain Injury, sponsored by GE Healthcare. Completed at 7 sites in United States. Open to participants aged 15 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-09-10.
Sponsored by GE Healthcare · Not applicable, Interventional, and Other
This is an open-label, non-randomized, prospective, multi-site, parallel group (segment), hypothesis-generating study designed to collect data that will aid in future scientific and engineering exploration of correlations between clinical neuropsychological assessments and GE Research Pack II advanced MR imaging in mTBI patients. The results are primarily intended for scientific inquiry and engineering development purposes, and may be used in future regulatory submissions.
This data-driven study is being conducted for hypothesis generation in population of mild traumatic brain injury (mTBI) patients using advanced applications for magnetic resonance imaging (MRI) developed by the Sponsor, GE Healthcare (GEHC), and corresponding clinical neuropsychological assessments. This data is intended for future use in development of specialized MR acquisition, reconstruction, and processing software intended to identify mTBI biomarkers.
550 studies on the registry are indexed under Brain Concussion; 154 are open to participants now.
This study's enrollment of 477 is above the median of 64 across 376 interventional studies indexed under Brain Concussion.
Browse Brain Concussion studies →GE Healthcare is the lead sponsor of 175 studies on the registry; 20 are open to participants now.
Of its 19 completed or terminated interventional studies of FDA-regulated products, 16 (84%) have results posted.
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Subjects included as mTBI patients (Segment 1) will:
Subjects included as non-mTBI controls (Segment 2) will:
Exclusion Criteria:
Subjects will be excluded that have: mTBI
Contraindications to MRI scanning, including:
Subjects will be excluded that have:- non-TBI (controls)
1.5T or 3.0T MRI brain scanning with research sequences at 3 to 4 intervals in the acute period, with psychological cognitive evaluations at each MR visit Patients in the acute period following recent diagnosis of mild traumatic brain injury (mTBI)
Procedure: MRI
Control subjects with no recent mild traumatic brain injury. 1.5T or 3.0T MRI brain scanning with research sequences at 3 to 4 intervals in the acute period, with psychological cognitive evaluations at each MR visit
Procedure: MRI
MRI scanning
MRI Image Data Sets
MRI image data sets collected from subjects who completed the study.
Time frame: Per patient scanning over 3 months
Neuropsychological Assessments
Neuropsychological assessments collected from subjects who completed the study.
Time frame: Per patient scanning over 3 months
| Milestone | mTBI Patient Group (Segment 1) | Non-TBI Patients (Segment 2) |
|---|---|---|
| Started | 325 | 152 |
| Completed | 42 | 91 |
| Not completed | 283 | 61 |
| Withdrew: Subjects did not complete all 4 visits | 283 | 61 |
MRI image data sets collected from subjects who completed the study.
| Images collected | mTBI Patient Group (Segment 1) | Non-TBI Patients (Segment 2) |
|---|---|---|
| Study Visit 1 images collected | 79 | 150 |
| Study Visit 2 images collected | 290 | 111 |
| Study Visit 3 images collected | 240 | 105 |
| Study Visit 4 images collected | 218 | 118 |
| Total number of images collected | 827 | 484 |
Neuropsychological assessments collected from subjects who completed the study.
| Neuropsychological assessments | mTBI Patient Group (Segment 1) | Non-TBI Patients (Segment 2) |
|---|---|---|
| Visit 1 Neuropsychological assessments | 84 | 152 |
| Visit 2 Neuropsychological assessments | 303 | 114 |
| Visit 3 Neuropsychological assessments | 244 | 107 |
| Visit 4Neuropsychological assessments | 222 | 119 |
| Total number of Neuropsychological assessments | 853 | 492 |
Collected over Each visit lasted approximately 90 minutes.. Non-serious events are listed at a 0% frequency threshold.
| Group | Deaths | Serious | Other |
|---|---|---|---|
| mTBI Patient Group (Segment 1) | 0/325 (0%) | 0/325 (0%) | 22/325 (6.8%) |
| Non-TBI Patients (Segment 2) | 0/152 (0%) | 0/152 (0%) | 1/152 (0.7%) |
| Event | mTBI Patient Group (Segment 1) | Non-TBI Patients (Segment 2) |
|---|---|---|
| ClaustrophobiaNervous system disorders | 7/325 | 1/152 |
| Peripheral Nerve StimulationNervous system disorders | 5/325 | 0/152 |
| PainGeneral disorders | 3/325 | 0/152 |
| ConcussionNervous system disorders | 3/325 | 0/152 |
| HeadacheGeneral disorders | 2/325 | 0/152 |
| AnxietyPsychiatric disorders | 1/325 | 0/152 |
| ACL tearMusculoskeletal and connective tissue disorders | 1/325 | 0/152 |
Segment 1 consisted of adolescent and adult mTBI patients who recently sustained head injury. Segment 2 consisted of subjects who were enrolled as a control population.
| Age, Categorical(Participants) | mTBI Patient Group (Segment 1) | Non-TBI Patients (Segment 2) | Total |
|---|---|---|---|
| <=18 years | 168 | 76 | 244 |
| Between 18 and 65 years | 149 | 63 | 212 |
| >=65 years | 0 | 0 | 0 |
| Sex: Female, Male(Participants) | mTBI Patient Group (Segment 1) | Non-TBI Patients (Segment 2) | Total |
|---|---|---|---|
| Female | 141 | 76 | 217 |
| Male | 176 | 63 | 239 |
| Race and Ethnicity Not Collected(Participants) | mTBI Patient Group (Segment 1) | Non-TBI Patients (Segment 2) | Total |
|---|---|---|---|
| Count of participants | — | — | 0 |
| Region of Enrollment(participants) | mTBI Patient Group (Segment 1) | Non-TBI Patients (Segment 2) | Total |
|---|---|---|---|
| United States | 325 | 152 | 477 |
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