What to Expect

 These rules are used to find people who may benefit, keep out people who may be harmed, and help researchers find the information they need. If you are found eligible, the investigator will then sit with you to explain the details of the clinical trial, particularly describing the risks and benefits of the study, the type of procedures or tests during the study and the number of visits involved throughout the study period. Once you fully understand of the clinical study, you will be required to sign a consent form. Patient will also be provided a summary of the Consumer Bill of Rights and Responsibilities that was adopted by the US Advisory Commission on Consumer Protection and Quality in the Health Care Industry in 1998. It is also known as the Patient’s Bill of Rights. This will also be signed by each study subject.