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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03968445
Other study ID # IRB-300003221 R19-045
Secondary ID
Status Active, not recruiting
Phase Phase 1
First received
Last updated
Start date October 17, 2019
Est. completion date July 24, 2025

Study information

Verified date February 2024
Source University of Alabama at Birmingham
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to see if positron emission tomography and magnetic resonance imaging (PET/MRI) with an investigational drug called [18F]DPA-714 will show inflammation in the brain after a heart attack. This study may help physicians and researchers better understand the role of brain inflammation in heart disease and develop new treatments to protect the brain.


Description:

The primary objective of this study is to measure the concentration and the regional brain distribution of activated brain microglia/macrophages using the PET ligand [18F]DPA-714 in individuals with recent AMI. The basic premise is that AMI leads to systemic inflammation that includes inflammation in the brain. The PET tracer [18F]DPA-714 binds to the 18 kDa translocator protein (TSPO, also known as the peripheral benzodiazepine receptor) in the mitochondria of activated microglia/macrophages and provides a non-invasive measure of neuroinflammation. The estimates of brain TSPO binding in patients with recent AMI will be compared to a matched group of patients who have undergone a recent elective PCI procedure.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 6
Est. completion date July 24, 2025
Est. primary completion date October 24, 2024
Accepts healthy volunteers No
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria: 1. Participation in UAB IRB protocol "Neuroinflammation After Acute Myocardial Infarction" (IRB-300002751, PI Lazar). 2. 21 years of age or older 3. . English speaking with at least 8th grade education 4. High or mixed affinity binder for TSPO ligands based on genotyping for single nucleotide polymorphism (SNP) rs6971. 5. Admission to UAB Hospital for ST-elevation acute myocardial infarction (AMI) and treatment with percutaneous coronary intervention (PCI) OR Undergoing elective percutaneous coronary intervention (PCI) Exclusion Criteria: 1. Contraindication to MRI 2. Pregnancy 3. Lactation 4. Serious medical co-morbidity that may interfere with participation 5. Prior myocardial infarction 6. Severe anemia 7. Prior coronary artery bypass grafting 8. Prior angioplasty and/or coronary artery stent placement (PCI group only) 9. History of traumatic head injury defined by a loss of consciousness =30 minutes or seizure at the time of injury 10. Diagnosis of major depression 11. Diagnosis of dementia 12. Low affinity binder for TSPO ligands based on genotyping for SNP rs6971.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
[18F]DPA-714-PET/MRI
[18F]DPA-714-PET/MRI

Locations

Country Name City State
United States University of Alabama at Birmingham Medical Center Birmingham Alabama

Sponsors (1)

Lead Sponsor Collaborator
University of Alabama at Birmingham

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary TPSO-PET measurement of neuroinflammation after acute myocardial infarction The regional brain concentrations of [F-18]DPA-714, a PET imaging marker of neuroinflammation, will be compared between study participants who have recently been hospitalized for acute myocardial infarction (AMI) and a control group undergoing elective percutaneous coronary interventions (PCI). 2 years
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