Actively Recruiting

Phase 1
Age: 18Years - 70Years
All Genders
Healthy Volunteers
NCT06920628

PET Imaging of Cyclooxygenase-1 in Participants With Neurological Manifestations of Post-Acute Sequelae of SARS-CoV-2 Infection (PASC)

Led by National Institute of Mental Health (NIMH) · Updated on 2026-03-03

60

Participants Needed

1

Research Sites

192 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Background: SARS-CoV-2 is the virus that causes COVID-19. Some people who recover from COVID-19 have long-term symptoms that affect the brain. These include headaches; loss of taste and smell; sleep problems; thinking problems; depression; and anxiety. Researchers want to know if a tracer (a substance that is injected into a person s body before an imaging scan) can help identify inflammation in people with these brain disorders. Objective: To see if a radioactive tracer (\[11C\]PS13) can highlight brain inflammation in those who had COVID-19 but still have symptoms that affect the brain. Eligibility: Adults aged 18 to 70 years with post COVID-19 brain disorders who are enrolled in protocol 000089 or 000711. Healthy volunteers are also needed. Design: Participants will have up to 5 clinic visits. Participants will be screened. They will have blood tests and a test of their heart function. They will have imaging scans: Magnetic resonance imaging (MRI): They will lie on a table that slides into a metal tube. Pictures will be taken of the brain. Positron emission tomography (PET): A needle attached to a thin tube will be inserted into a vein in the arm. The tracer will be injected through the tube. Another needle attached to a thin tube will be inserted into the wrist or inside of the elbow of the other arm to draw blood. They will lie still on a bed while a machine captures images of their brain. The scan will last about 2 hours. Study involvement is 11 to 14 weeks....

CONDITIONS

Official Title

PET Imaging of Cyclooxygenase-1 in Participants With Neurological Manifestations of Post-Acute Sequelae of SARS-CoV-2 Infection (PASC)

Who Can Participate

Age: 18Years - 70Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18 to 70 years
  • In good general health based on medical history and physical exam
  • Able to understand and consent to all required tests and examinations
  • For Neuro-PASC participants: enrolled in specific protocols and diagnosed with Neuro-PASC
  • Have adequate ulnar collateral blood flow and no metal or foreign objects in both wrists
  • Agree to follow lifestyle considerations
  • For healthy volunteers: aged 18 to 70 years, able to consent, good general health with no cognitive impairment
  • No active SARS-CoV-2 infection; at least six weeks since symptom onset with no fever for at least one week
  • Report at least one prior SARS-CoV-2 infection
  • Enrolled in specified healthy volunteer protocols
  • Have adequate ulnar collateral blood flow and no metal or foreign objects in both wrists
  • Agree to follow lifestyle considerations
Not Eligible

You will not qualify if you...

  • Clinically significant abnormalities on EKG or laboratory tests, including elevated creatinine (>1.3 mg/dL)
  • Use of NSAIDs within two weeks prior to PET scan
  • Use of corticosteroids or immunosuppressants within one month prior to PET scan
  • Substance use disorder or alcohol use disorder that impairs daily life
  • Unstable medical conditions making participation unsafe
  • Unable to travel to NIH
  • Recent exposure to research-related radiation exceeding limits
  • Inability to lie flat and still for at least two hours (including claustrophobia or weight limits)
  • Unable to have MRI due to implanted devices or metal fragments
  • Pregnancy or breastfeeding
  • HIV infection

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

National Institutes of Health Clinical Center

Bethesda, Maryland, United States, 20892

Actively Recruiting

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Research Team

T

Tara N Turon, C.R.N.P.

CONTACT

R

Robert B Innis, M.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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