Sacramento, CANCT06014515Now EnrollingIRB Ready

Healthy Subjects Clinical Trial in Sacramento, CA

Access cutting-edge healthy subjects treatment through this clinical trial at a research site in Sacramento. Study-provided care at no cost to qualified participants.

Sponsored by University of California, Davis

Quick Self-Assessment

See if you qualify for this Sacramento location

Preparing your pre-screening questions…

Expert Care in Sacramento

Access healthy subjects specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related healthy subjects treatment provided free

Apply for This Sacramento Location

Check if you qualify for this healthy subjects clinical trial in Sacramento, CA

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Sacramento

    Convenient for CA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Sacramento site if eligible
  4. 4Begin participation

About This Healthy Subjects Study in Sacramento

The overarching goal of this project is to develop and evaluate a single-tracer multiparametric positron emission tomography (PET) imaging solution for simultaneous imaging of blood flow and glucose metabolism using 18F-fluorodeoxyglucose (FDG) alone. The investigators working hypothesis is that quantitative blood flow can be extracted from dynamic 18F-FDG PET data by use of tracer kinetic modeling, in addition to glucose metabolism that 18F-FDG is conventionally used for.

Sponsor: University of California, Davis

Who Can Participate

Inclusion Criteria

Adults (age ≥ 18 years old)
Ability to understand and willingness to sign an informed consent form
Ability to adhere to the study visit schedule and other protocol requirements.
Willing and able to fast for at least 6 hours before and for the duration of the scan
No strenuous exercise for 24 hours prior to being scanned
Willing to lie on the scanner bed for up to 60 minutes
Free of active COVID-19 symptoms
Patients with clinically acute or chronic conditions such as cardiovascular, cardiometabolic, or cardiopulmonary diseases, which may include but are not limited to ischemic heart disease, myocarditis, arrhythmias, heart failure, nonalcoholic fatty liver disease, COVID-related sequala, diabetes, hypertension, or renal disease that would result in changes in normal tissue perfusion and/or metabolism.

Exclusion Criteria

Participants are not eligible if they meet ANY of the following criteria:
Self-reported history of dysphoria or anxiety in closed spaces
Body weight \>240 kg due to limitations of the scanner bed
Pregnant or breast-feeding (due to risks of ionizing radiation; urine pregnancy test will be administered prior to start of each PET/CT session for all participants between 18 to 60 years old who are able to get pregnant, unless documented hysterectomy or bilateral ovarian removal is available)
Blood glucose greater than 200 as assessed by fingerstick method before injection of 18F-FDG
Concurrent or prior enrollment in a separate research study involving a PET scan performed within the last 12 months for research purposes only.
Any condition that would prevent the understanding or rendering of informed consent.
Any comorbidity that, in the opinion of the investigator, could compromise protocol objectives.

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 (NCT06014515) 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.

Healthy Subjects Treatment Options in Sacramento, CA

If you're searching for healthy subjects treatment options in Sacramento, CA, this clinical trial (NCT06014515) 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 healthy subjects 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 healthy subjects clinical trials near you to find additional studies recruiting in your area.

More Carpal Tunnel Trials in Sacramento, CA

See all carpal tunnel clinical trials recruiting in Sacramento — not just this study.

Browse Carpal Tunnel Trials in Sacramento

Browse More Trials by Condition

Ready to Join in Sacramento?

Take the first step toward participating in this groundbreaking clinical trial

Secure · Expert Care · Sacramento, CA