Clinical research trials here in Charlotte
Here are some common questions and answers about clinical research trials.
What are clinical trials and why do people participate?
Clinical research is medical research that involves people like you. When you volunteer to take part in clinical research, you help doctors and researchers learn more about the disease and improve health care for people in the future. Clinical research includes all research that involves people.
The goal of clinical research is to determine if a new test or treatment works and is safe. Clinical trials can look at other aspects of care, such as improving the quality of life for people with chronic illnesses.
Why do people participate in a clinical trial?
People participate in clinical trials for a variety of reasons. Healthy volunteers say they participate to help others and to contribute to moving science forward. Participants with an illness or disease also participate to help others, but also to possibly receive the newest treatment and to have the additional care and attention from the clinical trial staff.
Clinical researches offer hope for many people and an opportunity to help researchers find better treatments for others in the future.
Clinical research can study:
- New drugs or new combinations of drugs
- New ways of doing surgery
- New medical devices
- New ways to use existing treatments
- New ways to change behaviors to improve health
- New ways to improve the quality of life for people with acute or chronic illnesses.
How does the research process work?
Clinical research often starts in the lab. After researchers test new treatments or procedures in the lab and animals, the most promising treatments are moved into clinical trials. As new treatments move through a series of steps called phases, more information is gained about the treatment, its risks, and its effectiveness.
What are clinical trial protocols?
Clinical trials follow a plan known as a protocol. The protocol is carefully designed to balance the potential benefits and risks to participants and answer specific research questions.
What is informed consent?
Informed consent is the process of providing you with key information about a research study before you decide whether to accept the offer to take part. The process of informed consent continues throughout the study.
Clinical research trials at top Charlotte dermatologist
Charlotte, NC residents may consider clinical research as a good option for them. Your doctor can recommend you for a trial they are aware of or you can inquire by contacting the office. If you are a good fit, you can be of great help to future patients, have successful treatments and even find cures for diseases. Contact Dermatology Specialists of Charlotte, Charlotte’s top Ballantyne and Blakeney Dermatologist, for your dermatology care and find out more about our clinical researches.