Patient Information

 Participating in a clinical trial offers several potential benefits, including access to cutting-edge treatments and therapies, expert medical care, and the opportunity to contribute to the advancement of medical knowledge. Clinical trials also offer hope for individuals with conditions for which there are currently limited treatment options. 

 Before participating in a clinical trial, it's important to understand what to expect. Clinical trials involve carefully planned research studies that follow strict scientific standards. Participants may receive investigational treatments or placebos, and their health will be closely monitored throughout the study. 

 We understand that participating in a clinical trial can be a significant decision. That's why we provide resources and support to help you make an informed choice. Visit our Resources page for helpful information about clinical trials and what to expect as a participant. 

 nformed consent is a critical part of participating in a clinical trial. Before enrolling in a study, you will be provided with detailed information about the study, including its purpose, procedures, risks, and benefits. You will have the opportunity to ask questions and decide whether or not to participate. Your decision to participate is voluntary, and you can withdraw from the study at any time. 

 Protecting your privacy and confidentiality is a top priority. Your personal information and medical records will be kept confidential and will only be accessed by authorized personnel involved in the study. Your identity will be protected in all study-related publications and presentations. 

 Your safety is our top priority. Clinical trials are closely monitored to ensure that participants are not exposed to unnecessary risks. Safety measures are in place to minimize any potential risks, and your health will be closely monitored throughout the study 

 Participating in a clinical trial is typically free of charge for participants. In some cases, you may be reimbursed for your time and travel expenses. It's important to discuss any financial considerations with the research team before enrolling in a study. 

 As a research participant, you have certain rights and responsibilities. These include the right to receive clear and accurate information about the study, the right to ask questions and have them answered, and the responsibility to follow the study protocol and attend all study visits as required. 

 If you have any concerns or questions about your participation in a clinical trial, you can speak with a patient advocate. Patient advocates are available to help you understand your rights as a participant and address any concerns you may have.