Who is eligible for clinical trial NCT07527130?

Participants must meet protocol criteria for COVID-19. Confirm exact inclusion and exclusion requirements with the study coordinator.

Does clinical trial NCT07527130 provide travel or cost reimbursement?

Check with the site coordinator at the participating facility for travel and lodging stipend availability, and for which routine-care costs are covered.

🏛️ Verified NIH Record • Updated 2026-07-16

C11 ER176 PET in Evaluating Neuroinflammation in Patients With Post-COVID Syndrome (NCT07527130)

🟡 Not Yet Recruiting Interventional Protocol 📊 Observational Clinical Research Sponsor: Mayo Clinic

🩺 Plain-English Summary (8th-Grade Level)

The purpose of this research is to find out if Positron Emission Tomography (PET) imaging with an investigational drug called C-11 ER176 can help us learn more about Post-COVID Syndrome.

Who can join: To join this study, participants generally need to meet the listed inclusion criteria (3 items) and avoid the listed exclusions (12 items).

Location: Mayo Clinic — Rochester, Minnesota

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Check every box below. If you can check all of them, you may meet the study's basic screening requirements (final eligibility is confirmed by the site team).

Mayo Clinic patients with a previously confirmed infection with the novel SARS-CoV-2 virus who have been seen in the Post COVID Clinic through GIM Integrative Medicine \& Health Section or approval by MAGPIES research group.
Be able to participate fully in all aspects of the study.
Have understood and signed study informed consent.

Usually NOT eligible if any of the following apply:

Exclusion Criteria:
Lacking the capacity to consent.
Prisoners and institutionalized individuals.
Reports being currently pregnant, lactating, or are of child-bearing potential or are likely to become pregnant during the LLLT treatment phase and are unwilling to use a reliable form of contraception. o Acceptable forms include:
Hormonal methods, such as birth control pills, patches, injections, vaginal ring, or implants
Barrier methods (such as a condom or diaphragm) used with a spermicide (a foam, cream, or gel that kills sperm)
Intrauterine device (IUD)
Total hysterectomy or tubal ligation
Abstinence (no sex).
Those patients that have implants that would prevent them from having a PET Scan.
Patients that have claustrophobia.
Have a known history of any condition or factor judged by the investigator to preclude participation in the study or which might hinder adherence.

🔍 Extracted verbatim from the official NIH eligibility criteria. Always confirm with the study coordinator.

📍 All Participating Trial Locations (1 Sites)

Mayo Clinic — Rochester, Minnesota

💰 Cost, Insurance & Patient Rights

100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

🏛️ View Official NIH Record ↗