Clinical Trials
Your partner in finding life-changing medical treatments
Welcome to Orange County Research Center, and thank you for considering a vital role in advancing medicine. By participating in clinical trials, you’re helping to shape the future of healthcare and bring hope to countless others.
Our state-of-the-art facility in Lake Forest, California is dedicated to providing a safe, supportive, and comfortable experience for every participant. With over 30 years of experience in conducting Phase I–IV clinical trials, our expert team is here to ensure you feel informed, respected, and valued throughout your journey with us.
What is a clinical trial?
A clinical trial is a research study that uses volunteers to test new methods of screening, prevention, diagnosis, or treatment for a disease.
These trials are designed to answer key questions about new therapies or innovative uses for existing treatments. They also aim to determine whether new drugs or procedures are both safe and effective.
Carefully conducted clinical trials are the fastest and safest way to discover treatments that work for people.
Why should I participate in a clinical trial?
Clinical trials may offer alternatives when standard treatments have failed or caused intolerable side effects.
Contribute to groundbreaking research that could help others in the future.
- Take an active role in your healthcare
- Gain access to new research treatments
- Receive expert medical care for the condition being studied
- Help others by contributing to medical research
Other frequently asked questions about clinical trials
Is there financial compensation for participating in studies?
What can I expect at my first appointment?
During your initial appointment, you’ll complete administrative paperwork and a medical history review. This includes discussing your medical history — including any surgeries and/or hospitalizations — medications, and any past reactions to treatments. Please bring your current medications (prescription and over-the-counter) to the appointment.
The initial visit typically lasts between 90 minutes to 2 hours, though the exact duration may vary depending on the clinical trial you are screening for. After the evaluation, we’ll discuss available study options tailored to your medical history. You’ll also receive detailed information about the trial, including your role and responsibilities as a volunteer.
If a study interests you, we’ll provide an Informed Consent form for you to review. Feel free to ask any questions during the appointment, and you may also take the form home to discuss it with your family or doctor.
Once you decide to participate, if needed we’ll schedule your next appointment to begin the study.
