Full-Body scans reveal hidden immune clues in long COVID
NCT ID NCT07076862
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study uses a special full-body PET/CT scan to look for signs of immune system activity in people with Long COVID. Researchers will compare scans from 51 participants with and without Long COVID to see where the body might be inflamed. The goal is to better understand what causes Long COVID symptoms and find ways to measure and treat it in the future.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- [¹⁸F]F-AraG (a radioactive tracer for PET imaging)
- What this could lead to
- If successful, this could lead to better ways to diagnose and monitor Long COVID by identifying where immune problems are happening in the body.
- What could go wrong
- This is a very early, small study (51 people) that is only looking at imaging, not testing a treatment. It may not find clear patterns or lead directly to new therapies.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Early phase 1
The earliest testing in people: a first look at safety, in a very small group.
- Participants
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About 51 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2025
- Expected to finish
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Dec 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age ≥ 18 years 2. Ability to understand the purposes and risks of the trial and willingness to sign an IRB-approved informed consent form. 3. Willingness and ability to comply with all protocol required procedures. 4. For participants of reproductive potential, defined as individuals who have not been post-menopausal for at least 24 consecutive months (i.e., who have had menses within the preceding 24 months), or women who have not undergone surgical sterilization, specifically hysterectomy and/or bilateral oophorectomy or bilateral salpingectomy, willingness to use effective double barrier contraceptive methods (excluding withdrawal or timing methods) during the study and up to 1 day after the last administration of the radiotracer. 5. Previous diagnosis of SARS-CoV-2 infection as defined by a prior positive SARS-CoV-2 nucleic acid-based diagnostic test performed in a clinical laboratory on one or more nasopharyngeal or respiratory secretion samples or from an FDA-approved rapid antigen test at home. Documentation of the positive test will be requested but not required; if not available the participant will be asked to attest to the presence of a positive test. 6. Onset of COVID-19 symptoms (or if no symptoms, time of initial nucleic acid or antigen-based diagnostic test) at least 3 months prior to the baseline study visit. 7. Ability to travel to our research sites in San Francisco and Sacramento. 8. Laboratory evaluations obtained within 60 days prior to entry: 1. Hemoglobin ≥ 8g/dL 2. Platelet count ≥ 75,000 cells/mm3 3. Absolute neutrophil count (ANC) \> 1000 cells/mm3 4. Aspartate aminotransferase (AST) \< 3 × ULN units/L 5. Alanine aminotransferase (ALT) \< 3 × ULN units/L 6. Calculated creatinine clearance (CrCl) ≥ 60mL/min as estimated by the Cockcroft-Gault equation: For men, (140 - age in years) × (body weight in kg) ÷ (serum creatinine in mg/dL × 72) = CrCl (mL/min)\* \*For women, multiply the result by 0.85 = CrCl (mL/min) 9. For PASC participants only: Reporting at least 2 unexplained symptoms, with at least 1 symptom in the fatigue domain and at least 1 symptom in either cardiopulmonary or neurocognitive domains, that last for at least 2 months and cannot be explained by an alternative diagnosis. Symptoms may be new onset after initial COVID-19 recovery or persist from the initial acute phase and may fluctuate or relapse over time. (According to World Health Organization definition of PASC http://www.WHO.int ) 10. For control participants only: Individuals who have made full clinical recovery within 4-12 weeks of acute COVID-19 infection with no newly developed symptoms or changes in health after recovery. Exclusion Criteria: 1. Serious comorbidities (nonmalignant disease or other conditions) that in the opinion of the investigator could compromise protocol objectives. 2. Any condition that alters the function of their immune system or any conditions caused by malfunction of their immune system and would interfere with imaging, including known underlying inflammatory or immune disorders, systemic malignancy, or other chronic viral infections (such as HIV, hepatitis B and hepatitis C). 3. Received vaccination of any type, including a SARS-CoV-2 vaccine, within 30 days of imaging 4. Pregnant or nursing individuals. A urine or HCG serum pregnancy test with a sensitivity of at least 25 mIU/mL will be performed at screening and on the day of PET/CT imaging at no charge to all participants of reproductive potential (see definition above). 5. Participants who have had prior allogeneic stem cell or solid organ transplant. 6. Previously diagnosed myelodysplasia syndrome or history of lymphoproliferative disease prior to study entry. 7. Active systemic autoimmune diseases not related to COVID-19. 8. Self-reported history of dysphoria or anxiety in closed spaces (i.e., uncontrolled claustrophobia). 9. Concurrent or prior enrollment in a separate research study involving a PET scan performed within the last 12 months for research purposes only. 10. Body weight is more than 240 kg (529 pounds) 11. Prisoners 12. Life expectancy \< 24 months 13. Recent use of medication including guanosine or cysteine analogs. 14. Any other criteria which would make the participant unsuitable for enrollment to this study, as determined by the Principal Investigator.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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UC Davis EXPLORER Molecular Imaging Center
RECRUITINGSacramento, California, 95816, United States
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University of California San Francisco
RECRUITINGSan Francisco, California, 94110, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Magnetic pulses may clear long COVID brain fog
- Could a common supplement ease long COVID in teens?
- Sniffing out COVID: new At-Home smell test could spot infections early
- Scientists hunt for hidden COVID remnants in long COVID patients
- Scientists probe brain fatigue in long COVID survivors
- Magnetic pulses to the brain may lift long COVID fog