Is NCT07076862 recruiting in Sacramento, CA?

Yes, NCT07076862 is currently recruiting participants at its Sacramento, CA location. This pasc post acute sequelae of covid-19 clinical trial is actively enrolling qualified participants.

Is participation in this Sacramento clinical trial free?

Yes, all study-related care is provided at no cost to qualified participants. Many studies also offer compensation for time and travel expenses.

PASC Post Acute Sequelae of COVID-19 Clinical Trial in Sacramento, CA

Q: How do I join the pasc post acute sequelae of covid-19 clinical trial in Sacramento?

To join this clinical trial in Sacramento, complete the eligibility form on this page. A study coordinator will contact you to discuss next steps and determine if you qualify.

About This PASC Post Acute Sequelae of COVID-19 Study in Sacramento

This study uses total-body \[¹⁸F\]F-AraG PET/CT imaging to investigate immune activation and vascular changes in individuals with post-acute sequelae of SARS-CoV-2 infection (PASC), also known as Long COVID. Participants will undergo dynamic PET/CT imaging along with blood biomarker assessments and symptom evaluations. The study aims to characterize sites of immunological perturbation, correlate PET imaging findings with peripheral blood markers, and evaluate longitudinal changes in tissue-based immune activity in relation to symptom patterns over time. Data from this study will improve understanding of tissue-level immune dysregulation in PASC and support future clinical tools for assessing and managing this condition.

Sponsor: University of California, Davis

Who Can Participate

Inclusion Criteria

Age ≥ 18 years

Ability to understand the purposes and risks of the trial and willingness to sign an IRB-approved informed consent form.

Willingness and ability to comply with all protocol required procedures.

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.

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.

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.

Ability to travel to our research sites in San Francisco and Sacramento.

Laboratory evaluations obtained within 60 days prior to entry:

Hemoglobin ≥ 8g/dL

Platelet count ≥ 75,000 cells/mm3

Absolute neutrophil count (ANC) \> 1000 cells/mm3

Aspartate aminotransferase (AST) \< 3 × ULN units/L

Alanine aminotransferase (ALT) \< 3 × ULN units/L

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)

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 )

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

Serious comorbidities (nonmalignant disease or other conditions) that in the opinion of the investigator could compromise protocol objectives.

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).

Received vaccination of any type, including a SARS-CoV-2 vaccine, within 30 days of imaging

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).

Participants who have had prior allogeneic stem cell or solid organ transplant.

Previously diagnosed myelodysplasia syndrome or history of lymphoproliferative disease prior to study entry.

Active systemic autoimmune diseases not related to COVID-19.

Self-reported history of dysphoria or anxiety in closed spaces (i.e., uncontrolled claustrophobia).

Concurrent or prior enrollment in a separate research study involving a PET scan performed within the last 12 months for research purposes only.

Body weight is more than 240 kg (529 pounds)

Life expectancy \< 24 months

Recent use of medication including guanosine or cysteine analogs.

Any other criteria which would make the participant unsuitable for enrollment to this study, as determined by the Principal Investigator.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Sacramento?

Yes, this clinical trial (NCT07076862) has an active research site in Sacramento, CA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

PASC Post Acute Sequelae of COVID-19 Treatment Options in Sacramento, CA

If you're searching for pasc post acute sequelae of covid-19 treatment options in Sacramento, CA, this clinical trial (NCT07076862) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Sacramento research site is actively enrolling participants for this clinical trial. You'll receive care from experienced pasc post acute sequelae of covid-19 specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all pasc post acute sequelae of covid-19 clinical trials near you to find additional studies recruiting in your area.

PASC Post Acute Sequelae of COVID-19 Clinical Trial in Sacramento, CA

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