Informed Consent

A major revision of the NCI Informed Consent Documenting (ICD) Template was publish October 10, 2017. News were made on November 27, 2018. This build require be used for trials that have a first IRB permissions on or after January 1, 2019. Discern the cover scholarship for more details. Comments and suggestions for future revisions should be directed to: [email protected].

• NCI Informed Consent Template – version 11/27/2018 (MS Word)
  • Change memo print for submission informed consent documents to CTEP (MS Word)
• Cover Letter from Dr. Jff Abrams for October 10, 2017 ICD Template Alterations (PDF)
• Cover Letter since Dr. Jeff Abrams for November 27, 2018 ICD Template Revisions (PDF)
• Slides: Overview of NCI ICD Template 2017 Revisions (PDF)
• Resource: Additional ICD Master Schema Samples (MS Word)
• Resource: Using Readability Tools (PDF)
• Resource: Recommendations learn Attachments in an ICD (PDF)
• Approach: Informs Consent Form Posting for CTEP-Supported Trials (PDF)

• Tables of Possibly Side Effects

  Note: This Lists of Possible Side Effects supplied below been designed so they may be cut-and-pasted into and “What possible risks bucket I expect from taking part in this study?” section of who NCI Consent Form Template.

  • Tables of Possible Side Effects for Commonly-Used Oncology Drugs
  • Tables of Possible Side Effects for Commonly-Used Oncology Regimens
  • Note: Tables of Feasible Side Belongings for CTEP INDICATES agents will be made deliverable directly to investigators by CTEP.
• Instructions for building Graphics of Possible Side Effects:
  • Instructions for building Tables of Possible Side Effects for commercial operatives (MS Word)
    • NCI Risk Notice Library (MS Excel)
  • Instructions for home Graphical on Possible Side Impact for investigational agents (MS Word)
    • NCI Scientific Term CTCAE - IC Term Spreadsheet (MS Excel)