A clinical trial is a research study that helps evaluate new medications, devices, or treatments. Participants volunteer to help researchers understand how these options work and whether they are safe and effective

Clinical trials move through several phases, each designed to answer different questions about a new medication or treatment:

• Phase 1: Tests a new treatment in people for the first time. Focuses on safety, side effects, and how the body processes the medication. Usually involves a small number of participants.

• Phase 2: Looks at whether the treatment works for a specific condition. Helps determine the best dose and continues monitoring safety. Includes more participants than Phase 1.

• Phase 3: Compares the new treatment to the current standard of care. Confirms effectiveness, monitors safety in a larger population, and gathers the data needed for FDA approval.

• Phase 4: Conducted after a treatment is approved and available to the public. Evaluates long‑term safety and real‑world effectiveness.

Your safety is our top priority. Every study is reviewed by an independent ethics board, monitored by medical professionals, and follows strict federal guidelines. You are closely monitored throughout the entire process.

Many studies offer compensation for your time and travel. The amount varies by study and will be communicated to you before you decide whether to participate.

Visit length depends on the study. Some visits take 15 minutes, while others may take 60 minutes or longer, dependent on the procedures that are required. We’ll give you a clear schedule before your first visit

No. Health insurance is not required to participate in clinical research. Study‑related care and procedures are provided at no cost.

Your first visit usually includes informed consent, a review of your medical history, and screening procedures to confirm eligibility. You’ll have plenty of time to ask questions before anything begins.

Yes. Participation is completely voluntary. You may withdraw at any time for any reason. We will ask for a reason if you decide to withdraw.

Absolutely. We follow HIPAA guidelines and so all of your personal information stored securely. Only authorized study staff and medical professionals have access to your records.

You’ll work with a dedicated coordinator, a board-certified investigator, and our clinical support team. We make sure you see familiar faces at each visit.

Your information will be reviewed and entered into our secure database. If there is missing information or questions, we will contact you for additional information. Once you are a match for a study, you will receive a call, email or text asking if you are interested in the study.

You may participate in multiple studies over time, but not at the same time. We’ll help you understand when you’re eligible for your next study.

We conduct a variety of clinical trials, including medication studies and device studies for chronic conditions and general health. These consist of, but not limited to:

Arthritis

Chronic Pain

Diabetes

Gout

High Blood Pressure

High Cholesterol

Heart Disease

IBS

Kidney Disease

Low Testosterone

Weight Loss

New studies open regularly. Joining our database is the best way to be notified when a study matches your profile

Some studies require changes to your current medications, while others do not. We will review your medication list and explain any requirements before you decide to participate.

Life happens. If you miss a visit, contact us as soon as possible. We’ll help you get back on schedule and keep your participation on track.

No. You can continue seeing your regular doctors. We can also share study‑related information with them if you choose.

Most procedures are simple and routine, such as blood draws, EKGs and vital signs. If a study includes anything more involved, we’ll explain it clearly before you decide.