Trialsphere

Join a Trial

Help bring novel medicines to the world by participating in one of our clinical trials.
*All of our trials are performed in CHANDLER

Current Studies

Sonusmed Hypertension Study (HIGH BLOOD PRESSURE)

Sponsored by SonusMed

Chronic Low Back Pain Study (Obesity/Overweight)

Sponsored by Eli Lilly
(GZQD |LBP | Triumph-7)

Early Alzheimer’s Study

Sponsored by Annovis

Menstrual Migraine Study

Sponsored by AbbVie (Mosaic)

Episodic/ Chronic Migraine Study

Sponsored by Ipsen (Meranti)

Upcoming Studies

Migraines

Multiple
Sclerosis

Painful Diabetic Neuropathy

Parkinson’s
Disease

Sign Up Form

Thank you for your interest in participating in one of our clinical trials. See if you may qualify by answering a few short questions. By filling out the interest form below, you consent to being contacted by our patient enrollment specialists via phone, text, or email with more information.












    FAQs

    Everything you need to know
    • Research studies that evaluate the safety and effectiveness of new medications in humans.
    • Before human testing, these potential treatments undergo rigorous lab animal testing to verify safety.
    • They are closely regulated by the US Food and Drug Administration (FDA). FDA approval is required for new treatments, ensuring they meet stringent quality and safety standards before public availability
    • In-depth Healthcare Attention: Benefit from closer health monitoring and personalized care from healthcare professionals throughout the trial.
    • Access to New Treatments: Gain early access to innovative treatments and contribute to the development of new medical therapies.
    • Complimentary Health Assessments: Receive free health screenings, lab tests, imaging, and exams, providing valuable insights into your health.
    • Contribute to Medical Advancements: Play a crucial role in advancing medical knowledge and treatments, helping to improve public health.
    • Safety and Volunteer Well-being: Enjoy the assurance of a safety-focused environment, with the option to withdraw at any time for your comfort.
    Yes, however, specific requirements and eligibility criteria exist for participating in clinical trials. Here are some key things to keep in mind about who can participate:
    • Age: There are often age minimums and maximums, depending on the study
    • Health status: To be eligible for the treatment, participants must have the medical condition that the treatment intends to alleviate. There are usually criteria around the type and severity of symptoms. Certain other health conditions may also exclude someone from participating if it could impact results
    • Gender: Some trials are limited to a single gender, especially early-stage trials testing drugs that interact differently with men vs. women
    • Prior treatments/therapies: Another criterion often considered is whether someone has undergone previous treatments related to the condition
    Ultimately, clinical trials set rigorous guidelines on age, health, gender and more. The specifics are narrowed down based on what they want to test and study for any potential new treatment. Getting enrolled can be selective.
    Benefits include:
    • Active participation in health care
    • Difficult to access and often costly treatments
    • Free testing (i.e. imaging, bloodwork, exams)
    • Assisting others by participating in trials for potential approval and public availability
    Participating in a clinical trial may carry risks your doctor will disclose. Possible risks of experimental treatment include:
    • Side effects, both known and unknown
    • Study procedures
    • Treatment ineffectiveness
    • Treatment is not practical for all patients
    Some clinical trials give patients a placebo instead of experimental treatment. Along with the risks above, the trial may need time and attention from participants, including trips to the research location, more treatments, hospital stays, or complex dosage requirements.
    Participating in a legitimate clinical study is free, and clinical studies do not require you to have health insurance in order to take part. While every effort is made to ensure that study-related costs are covered by the sponsor, unforeseen expenses may arise. For instance, if you experience side effects that require medical attention outside the study protocol, these costs may not be covered by the study. You are encouraged to discuss any questions or concerns with your health insurance provider and the research team before enrolling in the study
    Individuals who participate in clinical studies may receive compensation for their involvement. Compensation is provided for the time and effort outlined in the informed consent form, and the amounts can vary based on study length, required procedures, and participant needs. The sponsor sets the compensation amounts. Studies may also offer free medical checks, laboratory tests, and study medications. The current compensation system is not intended to incentivize taking personal risks, and any pressure to participate for payment is against ethical standards. Before enrolling in a study, the research site will disclose the compensation available for time and travel. Compensation should never be the main reason for participation; the primary goal should be helping to advance medical research.

    All potential volunteers should learn as much as possible about their disease and the clinical study they are considering. Participants are encouraged to ask questions of the research staff about the study, the care they can expect while participating, and the potential risks.

    The following questions may be helpful to discuss with the research team before enrolling:

    • What is the purpose of the study?
    • Why do the researchers believe the experimental treatment will be effective?
    • Has the treatment been tested previously?
    • What types of tests and experimental therapies will be used?
    • How do the study’s potential risks, side effects, and benefits compare to my current treatment?
    • How will my illness and the effectiveness of the treatment be tracked during the study?
    • How will this study affect my daily life?
    • How long will the study last?
    • Who will pay for the experimental treatment and other study-related costs?
    • Will I be compensated for my time, travel, or any additional expenses?
    • Will I receive the study results, and if so, when?
    • Who will be responsible for my healthcare during the study?
    • Whom should I contact on the study team if I have questions or concerns during participation?