Frequently Asked Questions (FAQ’s)

Many of these questions will be answered in the informed consent document associated with a specific clinical trial. This list of commonly asked questions is offered as a starting point for your discussions with our research team.

  • Who is the primary physician overseeing my medical care while I am participating in the trial?
  • Have my primary cardiologist and family doctor been consulted about this clinical trial?
  • Why do the physician-researchers involved in this study believe this new investigated treatment might be helpful?
  • Why was I selected to be a potential participant?
  • What does the “phase number” of the clinical trial mean to my participation?
  • Will I be hospitalized overnight as part of my participation?
  • Has a variation of this treatment or technique been tested before?
  • What are the possible risks, side effects and benefits of this therapy compared to my current treatment plan?
  • What are my options if I am injured by the new treatment or procedure?
  • What types of tests, appointments or procedures will be done at St. Vincent Heart Center?
  • How long will the study last?
  • Am I paid for my participation and/or reimbursed for expenses?
  • What type of long-term follow-up is planned for this study?
  • If I benefit from the new treatment, will I be allowed to continue receiving the drug medication after the trial ends?
  • When will I know the results of the clinical trial?
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