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Participating in Medical Research      |      Rights, Expectations and Resources
 
 

Rights and Expectations

As a research study participant, you have the right to:

  • Ask any questions you may have about the research study at any time
  • Have information about this research study provided in language that is understandable to you
  • Be told of the known potential side effects and adverse reactions of the investigational medicine
  • Receive a copy of the informed consent document
  • Stop participating in this research study at any time by withdrawing your consent

As a research study participant, you will be expected to:

  • Follow your research study team’s instructions, or notify them if you are unable to follow your instructions
  • Keep appointments with your research study team, or notify your team and reschedule if you cannot keep an appointment
  • Notify your research study team of any changes in your life that may make you ineligible to continue participation
  • Report any unexpected or severe side effects of the investigational medicine

RESOURCES

www.digestive.niddk.nih.gov
National Digestive Diseases Information Clearinghouse

www.ciscrp.org
Center for Information & Study on Clinical Research Participation

To view a map of all participating sites, CLICK HERE.

To view a map of all participating sites, CLICK HERE.
 
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