Welcome to Fresno Clinical Research Center

Where innovation meets compassion in the fight against fatty liver disease.

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The Fresno Clinical Research Center is at the forefront of fatty liver research, making significant contributions both nationally and within the Central California Valley. Our commitment to advancing medical knowledge has established us as a leading site for Phase 2, Phase 3, and Phase 4 clinical trials. With a strong track record of consistently ranking among the top enrolling sites in MASH, we are dedicated to understanding and addressing the complexities of fatty liver disease. We take pride in being a vital part of the evolving landscape of clinical research in this critical area of liver and gastrointestinal health.

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    FAQ(Frequently Asked Questions)

    The ethical and legal codes that govern medical practice also apply to clinical trials. Furthermore, most clinical research is federally regulated and includes built-in safeguards to protect participants. Each trial follows a carefully controlled protocol, which is a detailed plan outlining the researchers' actions throughout the study. As clinical trial progresses, researchers report the results at scientific meetings, in medical journals, and to various government agencies. Individual participants' names will remain confidential and will not be disclosed in these reports.

    Side effects are any undesired actions or effects resulting from the experimental drug or treatment. Adverse effects can include symptoms such as headaches, nausea, hair loss, skin irritation, or other physical issues. It is essential to evaluate experimental treatments for both immediate and long-term side effects.

    Benefits
    Well-designed and well-executed clinical trials offer eligible participants several advantages:
    • Active Role in Healthcare: Participants can take an active role in their own health care.
    • Access to New Treatments: They gain access to new research treatments before these options are widely available.
    • Expert Medical Care: Participants receive expert medical care at leading healthcare facilities during the trial.
    • Contribution to Medical Research:By participating, they help advance medical research and contribute to the wellbeing of others.
    Risks
    While there are many benefits, participating in clinical trials also involves certain risks:
    • Side Effects: Participants may experience unpleasant, serious, or even life-threatening side effects from the experimental treatment.
    • Effectiveness: The experimental treatment may not be effective for the participant.
    • Time and Commitment: The trial protocol may require more time and attention than standard treatments, including additional trips to the study site, more treatments, potential hospital stays, or complex dosage requirements.

    The clinical trial process varies depending on the type of trial being conducted (see “What are the different types of clinical trials?”). The clinical trial team typically includes doctors, nurses, and other healthcare professionals. They assess the participant's health at the beginning of the trial, provide specific instructions for participation, monitor the participant closely throughout the trial, and maintain communication after the trial is completed.

    Some clinical trials may involve more tests and doctor visits than what a participant would typically experience for their illness or condition. In all types of trials, participants work closely with the research team. Successful participation in a clinical trial relies on following the protocol carefully and maintaining frequent contact with the research staff.

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