Keywords
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Table of contents
  1. 1. Clinical Trial
  2. 2. Routine Documentation
  3. 3. Registry/Cohort Study
  4. 4. Quality Assurance
  5. 5. Data Standard
  6. 6. Patient-Reported Outcome
  7. 7. Medical Specialty
Selected data models

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- 9/24/15 - 1 form, 9 itemgroups, 72 items, 1 language
Itemgroups: Stratification, PATIENT CRITERIA, Consents I, Exclusion Criteria, Organ Function - Non Hematological, Organ Function - Hematological, Inclusion Criteria, Stratification II, CONSENT FOR RESEARCH STUDIES
- 8/4/15 - 1 form, 12 itemgroups, 70 items, 1 language
Itemgroups: Header module, Visit, Protocol Administration, Patient Demographics/Pre-Treatment Characteristics, KRAS Results Contact, KRAS Results Contact (alternate), Eligibility Check, Contraindications, Pre-Randomization Check, The following will also be recorded:, The following will also be recorded:, Protocol Design