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N/A N=477 Other

Advanced MRI Applications for Mild Traumatic Brain Injury-Phase 2

Concussion · Traumatic Brain Injury

Enrolled (actual)
477
Serious AEs
0.0%
Results posted
Sep 2019
Primary outcome: Primary: MRI Image Data Sets — 79; 150; 290; 111 Images collected

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
MRI (Procedure)
Age
Pediatric, Adult · 15+ yrs
Sex
All
Sponsor
GE Healthcare
Primary completion
Jan 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
MRI Image Data Sets
79; 150; 290; 111; 240; 105
PRIMARY
Neuropsychological Assessments
84; 152; 303; 114; 244; 107

Summary

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.

Eligibility Criteria

Inclusion Criteria

Subjects included as mTBI patients (Segment 1) will:

  • Be aged ≥15 and ≤50 years old at the time of enrollment;
  • Be diagnosed with mTBI according to the standard diagnostic procedures at the investigational site in a timeframe that meets enrollment criteria for enrollment within 72 hours (Visit 1) or 7±2 days (Visit 3) from injury.
  • Be capable of sufficiently clear communication and language fluency to allow the subject to provide written informed consent, or assent with parental or guardian consent for minors, and to complete study assessments (as per Section 6.3 - Protection of Vulnerable Subjects) for participation in all parts of the study.

Subjects included as non-mTBI controls (Segment 2) will:

  • Be aged ≥15 and ≤50 years old at the time of enrollment;
  • Are of similar characteristics as the mTBI population in terms of gender, age, handedness, educational level, and scanner criteria (as per Section 6.1.1 Enrollment of non-mTBI controls)
  • Be capable of sufficiently clear communication and language fluency to allow the subject to provide written informed consent, or assent with parental or guardian consent for minors, and to complete study assessments (as per Section 6.3 - Protection of Vulnerable Subjects), for participation in all parts of the study.

Exclusion Criteria

Subjects will be excluded that have: mTBI

  • Loss of consciousness (LOC) ≥5 minutes;
  • Posttraumatic amnesia lasting ≥24 hr following mTBI;
  • Current or prior (within past 10 years) moderate to severe TBI
  • Diagnosis of mTBI within the past 6 months;
  • Epilepsy with recurring seizures in past 10 years;
  • Drug abuse (except marijuana) in past 10 years based on DAST-10 screening;
  • Alcohol abuse based on AUDIT-C screening;
  • Current primary Axis I or II psychiatric disorders, except for disorders classified as minor and not expected to impact study conduct or integrity (as detailed in Appendix C - Screening Axis I/II Disorders):
  • History of brain mass, neurosurgery, stroke, white matter disease, and/or dementia;
  • Known cognitive dysfunction or structural brain disease/malformation;
  • Structural brain injury on prior neuroimaging findings;
  • Been prescribed antipsychotic/antiepileptic medications;
  • Unable (such as due to urgent medical care needs) or unwilling to complete study procedures accurately or have any conflict of interest that could affect study results, in the opinion of the investigator;
  • Contraindications to MRI scanning, including:
  • Current or suspected pregnancy, per site practice;
  • Other conditions that may constitute a hazard to the subject during study participation, per investigator;
  • Inability to comply with any part of the site's MR safety policy.

Subjects will be excluded that have:- non-TBI (controls)

  • Diagnosis of mTBI within the past 6 months;
  • Prior (within past 10 years) moderate to severe TBI (GCS <13);
  • Epilepsy with recurring seizures in past 10 years;
  • Drug abuse (except marijuana) in past 10 years based on DAST-10 screening;
  • Alcohol abuse based on AUDIT-C screening;
  • Current primary Axis I or II psychiatric disorders, except for disorders classified as minor and not expected to impact study conduct or integrity (as detailed in Appendix C - Screening Axis I/II Disorders):
  • History of brain mass, neurosurgery, stroke, white matter disease, and/or dementia;
  • Known cognitive dysfunction or structural brain disease/malformation;
  • Structural brain injury on prior neuroimaging findings;
  • Been prescribed antipsychotic/antiepileptic medications;
  • Unable (such as due to urgent medical care needs) or unwilling to complete study procedures accurately or have any conflict of interest that could affect study results, in the opinion of the investigator;
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02556177). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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