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You must include each of the following types of documents in order to register your Complete trial:
- Complete protocol document
- Participating sites (if not included in the protocol document). Multi-site trials require a list of participating sites and contact information.
Informed Consent (complete trials only, if not included in the protocol document)
Info If the Informed Consent and/or Participating Sites are not included as part of the protocol document, upload them separately as "Trial-Related Documents."
Currently you are required to supply your documents as Microsoft Word (.doc, .docx, or .docm), Adobe PDF, Microsoft Excel (.xls, .xlsx, .xlsm, or .xlsb), and/or WordPerfect files. Use the .xls format for template files.
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Adobe PDF files require special processing. Please see the information about creating PDFs in Converting Documents to PDFs . |
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Add Trial Page – Trial Related Documents for Abbreviated Trials
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The CTRO no longer supports Abbreviated trial templates. Please register Abbreviated trials in the CTRP Clinical Trial Registration application, and use the "Add my Site" feature instead of the Abbreviated Trial Participating Sites Template. |
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