What to Expect

Clinical Trial Expectations

• What will my responsibilities be as a participant?

  Our research and clinical trials are made possible by brilliant minds from multiple disciplines, all driven toward a common goal; improving healthcare for all. See the faces behind the latest innovations and get to know our research teams.

  There are some general responsibilities as a clinical trial participant. You will:

  • Make sure your contact information is accurate.
  • Attend all the scheduled appointments or inform the research staff in advance if you cannot attend an appointment.
  • Arrange your own transportation during the study.
  • Follow the directions of the researchers.
  • Reveal your past and present medical history if it is relevant to the study.
  • Discuss any questions or concerns with the researchers at any point throughout the trial.
  • Inform the research staff of any adverse events you experience while enrolled in the study.
  • Inform the Institutional Review Board Office if you feel your rights as a participant have been violated.

  Since every clinical trial is different, you might be asked to complete additional specific requirements if you choose to participate in a clinical trial.

• What will be my rights as a participant?

  You will have rights if you choose to participate in a clinical trial. You will have the right to:

  • Be treated with respect at all times.
  • Know the risk involved with the study participation.
  • Know what alternatives are available.
  • Withdraw from the study without any penalty.
  • Receive a sufficient amount of time to decide on participation.
  • Be informed of the name, credentials, and contact information of the principal investigator.
  • Be informed of the purpose of the study.
  • Be informed of who will have access to your information.
  • Be informed of what procedures may be performed and what drugs may be used.
  • Feel comfortable asking questions during any time of the study.