MANAGING HEPATITIS -- Clinical Trial Information

 

Informed consent is the process of learning the key facts about a clinical trial before you decide whether or not to participate. These facts include:

  • Why the research is being done.
  • What the researchers want to accomplish.
  • What will be done during the trial and for how long.
  • What risks are involved in the trial.
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  • What benefits can be expected from the trial.
  • What other treatments are available.
  • Your right to leave the trial at any time.

It is a good idea to take the consent documents home and discuss them with family members or friends. Talking about your options can help you feel comfortable with your decision. If you decide to join the clinical trial, be sure to ask for a copy of the informed consent documents so you can review them at any time.

Remember, informed consent is more than signing a form. It is a process that continues through the study. You should feel free to ask the research team questions before, during, and after the study. Informed consent continues as long as you are in the study.


All information provided in this site is offered for educational purposes only, and it is not intended nor implied to be a substitute for professional medical advice. Always consult your own physician or healthcare provider with any questions you may have regarding a medical condition.