What Happens During a Study?

Participating in a clinical trial is similar to a regular visit to your doctor. During your visits to HRHR you will initially meet with a research coordinator. The coordinator will discuss the study with you and explain in detail what to expect during the trial including your responsibilities. You will be presented facts about the study drug(s) and an informed consent form to read and sign. This is required by law to make sure you understand what is involved in a trial. Your medical history will be reviewed. If you qualify for study participation, you will be given a physical exam, blood and urine samples may be taken, and other specialized tests performed. The coordinator will also review your current medications. Depending on test results, which may not be known until after multiple visits, you will receive the investigational medication with detailed instructions on how to take it. As the study progresses you will meet with your study coordinator and physician at scheduled visits to discuss what has happened since your previous visit. This offers you the opportunity to ask questions and allows the coordinator to review your compliance with taking the medication and following the study requirements.