Attention Celerion eReg Portal Users:
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Clinical Trial Participant Responsibilities

Clinical Trial Participant Responsibilities

  • Completely read the consent form and ask the study staff any questions you may have. You should understand what will happen to you during the study before you agree to participate.
  • Follow all of the study restrictions and instructions.
  • Report to the clinic at assigned times.
  • Carefully weigh the possible benefits (if any) and risks of being in the study.
  • Talk to the study staff if you want to stop being part of the research study.
  • Report to the study staff immediately any and all problems you may be having with the study drug/procedure/device.
  • Do not become pregnant while participating in the study.
  • Do not get your partner pregnant while participating in the study.
  • Answer all questions honestly.