Getting-Started

Whatever the reason you have for wanting to participate in a clinical trial, Advanced Clinical Care is here to answer all of your questions. During the initial visit, you will meet with your research physician and go over your rights, disease or condition, and information about the clinical study.

During your meeting with the research physician, you will have an opportunity to ask as many questions you have. It’s our job to get you as informed as possible with your patient rights and clinical trial study and protocol. Additionally, you will be educated about your disease or condition and the goal of the clinical trial.

At this time, your research physician will go over the informed consent form. The informed consent form is a written agreement that is required by the FDA for all participants enrolling in a clinical trial. The form outlines information about the study including potential benefits and risks, the treatment plan, testing to be completed, patient rights and other information. It is important that you fully understand everything outlined in the form, so if you require additional time to go over the information, or would like to review with a family member or loved one, you will have as much time as you need. Any doubts, concerns or questions that arise during or after the initial meeting, you may call us and we will be glad to assist you.

If you are interested in participating in one of our clinical trials, please call or fill out the form on our website and we will help get you started.