Creedmoor Centre Endocrinology | 8340 Bandford Way Suite 001, Raleigh, NC 27615 | office:919.845.3332 | fax 888.714.0059 | Mon-Fri: 8a- 4:30p

Call Us: (919) 845-3332

What is Clinical Research?

Clinical research is a type of medical research that helps doctors learn better ways to prevent, diagnose, and treat health conditions. It often involves testing new medications, devices, or care approaches, or learning more about conditions that affect patients today. Clinical research follows strict safety guidelines and is carefully monitored to protect participants. 

What are the benefits of participating in a clinical trial?

Participating in clinical research can benefit patients in several ways. Some patients gain early access to new treatments that are not yet widely available, while also receiving close medical monitoring and care. Research participation helps advance medical knowledge, improve future treatments, and contributes to better care for other patients and families in the community.

What are the risks of participating in a clinical trial?

Participating in a clinical trial can involve some risks, which vary depending on the study. These may include side effects from medication, extra clinic visits, blood draws, or tests that may cause temporary discomfort. Some treatments being studied may not work as expected.

Before joining a study, the research team carefully explains all potential risks and benefits so patients can make an informed choice. Safety is carefully monitored throughout the trial, and information about your health is shared with you along the way. If at any point your doctor feels the risks outweigh the benefits, they may recommend stopping your participation.


Can I stop participating in a study once I have started?

Participation is always voluntary, and patients can choose to leave a study at any time.

I have concerns about how my rights are protected, what can I expect?

Your rights and safety are a top priority in clinical research. Before you join a study, you will go through an informed consent process where the research team explains the purpose of the study, what participation involves, and any potential risks or benefits. You will have time to ask questions and decide whether participating feels right for you.

Your personal health information is kept private, and studies are reviewed by independent oversight groups to ensure they are ethical and safe. Participation is always voluntary—you have the right to decline or leave the study at any time without it affecting your regular medical care.

Are there any costs associated with a clinical research trial, or will I be paid for my participation?

Costs and payment depend on the specific clinical research study. Most studies cover study‑related care, tests, or medications at no cost to you, and some may offer payment or reimbursement for time or travel. Before you decide to participate, the research team will clearly explain any costs and compensation so you can make an informed choice.

How do I inquire about current research taking place at CCE?

We provide a current list of trials on our website. You may also speak with our research staff by contacting us at research@ccendocrinology.comor call 919-845-3332.

Frequently Asked Questions