Please be sure to bring the proper identification to your initial visit. During this visit you will be given an Informed Consent Form. You will sit in a private room with the doctor or a study coordinator to discuss the purpose of the study, the risks, benefits, known side effects, as well as all procedures that will take place during the clinical trial.
Once the consent form has been explained, discussed and signed by all applicable parties (some clinical trials require a caregiver or other such person to be present during this process) you will begin the procedures of the actual study or be scheduled to come in another day depending study requirements.