Imaging of Traumatic Brain Injury Metabolism Using Hyperpolarized Carbon-13 Pyruvate (HPTBI)
Primary Purpose
Traumatic Brain Injury
Status
Enrolling by invitation
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
Hyperpolarized [1-13C] Pyruvate
Hyperpolarized [2-13C] Pyruvate
Sponsored by
About this trial
This is an interventional basic science trial for Traumatic Brain Injury focused on measuring Traumatic Brain Injury, TBI
Eligibility Criteria
Inclusion Criteria:
TBI Patients
- Injury occurred within 30 days
- Documented and verified TBI by Glascow coma scal 10-15 and/or Loss of Consciousness >10 minutes.
- Head Computed Tomography at admission.
ALL Subjects:
- 18 through 60 years of age.
- Ability to understand the the willingness to sign a writteninformed consent.
- All races and ethnicities will be included; subjects must be able to read and speak either the English or Spanish language.
Exclusion Criteria:
- Non-traumatic structural brain abnormality identified on head CT.
- Metallic foreign bodies on the scalp or cranium which may interfere with MRI acquisitions.
- Penetrating TBI.
- Significant anatomic distortion of the brain identified on CT images, such as large hematomas, herniation, intraventricular hemorrhage, extensive subarachnoid hemorrhage, hydrocephalus.
- Significant polytrauma that would interfere with follow-up and outcome assessment.
- Patients on psychiatric hold.
- Major debilitating mental health disorders including, but not limited to schizophrenia and bipolar disorder that would limit compliance with study requirements.
- Major debilitating neurological disease including, but not limited to, stroke, CVA, dementia and tumor that would limit compliance with study requirements.
- Under influence of illicit drugs which are known to alter brain physiology/metabolism including, but not limited to cocaine, lysergic acid diethylamide (LSD), and marijuana at the time of MRI/MRSI scanning.
- Any contraindication per MRI Screening Form including
- Implants contraindicated at 3T, pacemakers
- Implantable Cardioverter Defibrillator (ICD)
- Claustrophobia
- Prisoners or patients in custody.
- Medically unstable including
- Heart failure
- Severe left ventricular outflow tract (LVOT) obstruction
- Unstable angina
- Pregnancy
- Lactating
- Subjects who are receiving any other investigational agents.
Sites / Locations
- UT Southwestern - Advanced Imaging Research Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Hyperpolarized [1-13C] Pyruvate
Hyperpolarized [2-13C] Pyruvate
Arm Description
Injection with hyperpolarized [1-13C] Pyruvate during MRI.
Injection with hyperpolarized [2-13C] Pyruvate during MRI.
Outcomes
Primary Outcome Measures
[1-13C]lactate-to-H13CO3- ratio from [1-13C]pyruvate or [2-13C]lactate-to-[5-13C]glutamate ratio from [2-13C]pyruvate
Product ratio maps of lactate from pyruvate in the brain of TBI patients as compared to those of healthy controls.
Secondary Outcome Measures
Full Information
NCT ID
NCT03502967
First Posted
April 11, 2018
Last Updated
September 14, 2023
Sponsor
University of Texas Southwestern Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT03502967
Brief Title
Imaging of Traumatic Brain Injury Metabolism Using Hyperpolarized Carbon-13 Pyruvate
Acronym
HPTBI
Official Title
Imaging of Traumatic Brain Injury Metabolism Using Hyperpolarized Carbon-13 Pyruvate
Study Type
Interventional
2. Study Status
Record Verification Date
September 2023
Overall Recruitment Status
Enrolling by invitation
Study Start Date
June 1, 2018 (Actual)
Primary Completion Date
June 30, 2025 (Anticipated)
Study Completion Date
June 30, 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Texas Southwestern Medical Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
This project is to evaluate sensitivity and specificity of hyperpolarized 13C-pyruvate as imaging agents of altered cerebral glycolysis and mitochondrial dysfunction and assess pyruvate utilization in mitochondria in Traumatic Brain Injury (TBI) patients.
Detailed Description
Aim 1:
Investigators will quantify changes in [1-13C]lactate and H13CO3- labeling following a bolus injection of hyperpolarized [1-13C]pyruvate during the time window of secondary injury to assess upregulated glycolysis. Due to heterogeneous presence and severity of damage by TBI, defining the injured brain region can be difficult. Therefore, the metabolite ratio maps ([product]/[pyruvate]) of TBI patients (n = 5) will be compared with those of healthy-controls (n = 3).
Hyperpolarized [2-13C]pyruvate will be examined in a separate group of TBI cohorts (n = 5) and healthy controls (n = 3), and [5-13C]glutamate, [1-13C]acetyl-carnitine, [1-13C]acetoacetate, and [1-13C]citrate from [2-13C]pyruvate will be quantified for assessing the altered mitochondrial metabolism. Imaging procedure with [2-13C]pyruvate is the same as the imaging with hyperpolarized [1-13C]pyruvate.
For both [1-13C]pyruvate and [2-13C]pyruvate studies, each subject will be imaged twice with a 45min interval for confirming the reproducibility of the methods and/or averaging to enhance the signal-to-noise ratios of 13C-metabolite maps.
Aim 2:
After the feasibility study (aim1) is completed, an intra-subject comparison study of [1-13C]pyruvate and [2-13C]pyruvate will be performed. Similar to the aim1, patients with post-TBI neurological disorders having normal or near-normal CT results (n = 6 patients) as well as normal brains of age/gender-matching healthy volunteers (n = 3) will be recruited. Each patient will be imaged twice (one with [1-13C]pyruvate and one with [2-13C]pyruvate with a 45min interval). PDH activity and the TCA cycling will be assessed from measured H13CO3- from hyperpolarized [1-13C]pyruvate and [5-13C]glutamate from [2-13C]pyruvate, respectively. The comparison of [1-13C]pyruvate and [2-13C]pyruvate will identify the detailed information of how pyruvate (and converted acetyl-CoA) is utilized in the mitochondria, and assess the utility and necessity of imaging hyperpolarized [2-13C]pyruvate in TBI, providing critical data for future grant applications and larger clinical trials.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Traumatic Brain Injury
Keywords
Traumatic Brain Injury, TBI
7. Study Design
Primary Purpose
Basic Science
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Model Description
TBI patients and healthy control subjects
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Hyperpolarized [1-13C] Pyruvate
Arm Type
Experimental
Arm Description
Injection with hyperpolarized [1-13C] Pyruvate during MRI.
Arm Title
Hyperpolarized [2-13C] Pyruvate
Arm Type
Experimental
Arm Description
Injection with hyperpolarized [2-13C] Pyruvate during MRI.
Intervention Type
Drug
Intervention Name(s)
Hyperpolarized [1-13C] Pyruvate
Other Intervention Name(s)
HP Pyruvate Injection
Intervention Description
Bolus injection of study drug
Intervention Type
Drug
Intervention Name(s)
Hyperpolarized [2-13C] Pyruvate
Other Intervention Name(s)
HP Pyruvate Injection
Intervention Description
Bolus injection of study drug
Primary Outcome Measure Information:
Title
[1-13C]lactate-to-H13CO3- ratio from [1-13C]pyruvate or [2-13C]lactate-to-[5-13C]glutamate ratio from [2-13C]pyruvate
Description
Product ratio maps of lactate from pyruvate in the brain of TBI patients as compared to those of healthy controls.
Time Frame
One visit of three hours: 2 bolus injections during MRI with 45 minute rest period between the two
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
TBI Patients
Injury occurred within 30 days
Documented and verified TBI by Glascow coma scal 10-15 and/or Loss of Consciousness >10 minutes.
Head Computed Tomography at admission.
ALL Subjects:
18 through 60 years of age.
Ability to understand the the willingness to sign a writteninformed consent.
All races and ethnicities will be included; subjects must be able to read and speak either the English or Spanish language.
Exclusion Criteria:
Non-traumatic structural brain abnormality identified on head CT.
Metallic foreign bodies on the scalp or cranium which may interfere with MRI acquisitions.
Penetrating TBI.
Significant anatomic distortion of the brain identified on CT images, such as large hematomas, herniation, intraventricular hemorrhage, extensive subarachnoid hemorrhage, hydrocephalus.
Significant polytrauma that would interfere with follow-up and outcome assessment.
Patients on psychiatric hold.
Major debilitating mental health disorders including, but not limited to schizophrenia and bipolar disorder that would limit compliance with study requirements.
Major debilitating neurological disease including, but not limited to, stroke, CVA, dementia and tumor that would limit compliance with study requirements.
Under influence of illicit drugs which are known to alter brain physiology/metabolism including, but not limited to cocaine, lysergic acid diethylamide (LSD), and marijuana at the time of MRI/MRSI scanning.
Any contraindication per MRI Screening Form including
Implants contraindicated at 3T, pacemakers
Implantable Cardioverter Defibrillator (ICD)
Claustrophobia
Prisoners or patients in custody.
Medically unstable including
Heart failure
Severe left ventricular outflow tract (LVOT) obstruction
Unstable angina
Pregnancy
Lactating
Subjects who are receiving any other investigational agents.
Facility Information:
Facility Name
UT Southwestern - Advanced Imaging Research Center
City
Dallas
State/Province
Texas
ZIP/Postal Code
75390
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
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Imaging of Traumatic Brain Injury Metabolism Using Hyperpolarized Carbon-13 Pyruvate
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