CTRP application users can ignore this page altogether; it is simply a wiki shortcut.
This page displays links to subject matter that is included, in context, in many of the web pages that constitute the CTRP application user's guides.
Getting Help
This page contains select topics that help you to understand and use the NCI CTRP Protocol Abstraction Site. You can find more comprehensive documentation in the NCI Clinical Trials Reporting Program Protocol Abstraction User's Guide.
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Logging In and Out of Protocol Abstraction v3.9.1
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Searching for Trials in the Clinical Trials Reporting Program v3.9.1
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Searching for Persons in PA v3.9.1
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Searching for Organizations in PA v3.9.1
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Viewing Trial Identification Details v3.9.1
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Main Steps for Validating Submitted Trials v3.9.1
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Validating Trial-Related Documents v3.9.1
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Validating Trial Status Details v3.9.1
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Validating Funding Details v3.9.1
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Validating Trial IND/IDE Details v3.9.1
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Validating Regulatory Information v3.9.1
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Validating Participating Sites v3.9.1
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Processing Trial History Information v3.9.1
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Processing Trial Milestones v3.9.1
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Processing On-Hold Information v3.9.1
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Abstracting General Trial Details v3.9.1
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Abstracting NCI-Specific Information v3.9.1
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Abstracting Regulatory Information v3.9.1
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Abstracting Human Subject Safety Information v3.9.1
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Abstracting IND/IDE Information v3.9.1
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Abstracting Trial Status Information v3.9.1
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Abstracting Funding Information v3.9.1
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Abstracting Participating Site Information v3.9.1
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Abstracting Collaborator Information v3.9.1
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Abstracting Trial-Related Documents v3.9.1
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Abstracting Trial Descriptions v3.9.1
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Abstracting Interventional Trial Outcome Measures v3.9.1
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Abstracting Non-Interventional Trial Outcome Measures v3.9.1
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Abstracting Interventional Trial Eligibility Criteria v3.9.1
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Abstracting Non-Interventional Trial Eligibility Criteria v3.9.1
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Abstracting Diseases/Conditions v3.9.1
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Abstracting Interventions v3.9.1
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Abstracting Arm Information v3.9.1
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Abstracting Group and Cohort Information v3.9.1
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Abstracting Sub-Groups v3.9.1
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Adding Summary 4 Anatomic Site Information v3.9.1
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Abstracting Markers v3.9.1
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Adding Markers v3.9.1
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Validating Abstractions v3.9.1
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Processing Requests for Admin Rights in the In Box v3.9.1
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Managing Accrual Access v3.9.1
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Managing Trial Record Ownership v3.9.1
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Viewing Audit Trails v3.9.1
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Processing New Marker Requests v3.9.1
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Accessing Registered User Details v3.9.1
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Abstracting Interventional Trial Design Details v3.9.1
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Abstracting Non-Interventional Trial Design Details v3.9.1
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Viewing Check-Out History Records v3.9.1
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Using the Administrative Abstractor's Dashboard v3.9.1
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Using the Scientific Abstractor's Dashboard v3.9.1
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Using the Administrative and Scientific Abstractor's Dashboard v3.9.1
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Using the Super Abstractor's Dashboard v3.9.1
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Managing Your Protocol Abstraction Account v3.9.1
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Creating Trial Associations v3.9.1
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Viewing Trial Summary Reports v3.9.1
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Managing Trial Record Ownership v3.9.1
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