Wiki99/clinical trials

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Key terms[edit]

To make Wikidata content more accessible in more languages, the following are suggested key Wikidata items for translation (demo).

These terms are arbitrarily chosen! If anyone has a glossary of key terms for international translation of clinical trials, then please share!

Basics[edit]

Clinical trials[edit]

Alternative collections[edit]

Glossary of Common Site Terms, a ClinicalTrials.gov guide[edit]

ClinicalTrials.gov Glossary of Common Site Terms (Q106891230) is a publication of ClinicalTrials.gov. As it is a work of the United States Federal Government, the text is in the public domain. Here are the list of terms matched to corresponding Wikidata items.

  1. Accepts healthy volunteers
  2. Active comparator arm
  3. Adverse event
  4. Age or age group
  5. All-cause mortality
  6. Allocation
  7. Arm
  8. Arm type
  9. Baseline characteristics
  10. Canceled submission
  11. Certain agreements
  12. Certification
  13. certification (Q374814)
  14. Certification/extension first posted
  15. Certification/extension first submitted
  16. Certification/extension first submitted that met QC criteria
  17. City and distance
  18. distance (Q126017)
  19. Clinical study
  20. Clinical trial
  21. ClinicalTrials.gov identifier (NCT number)
  22. Collaborator
  23. Condition/disease
  24. Contact
  25. Country
  26. Cross-over assignment
  27. Data Monitoring Committee (DMC)
  28. Early Phase 1 (formerly listed as Phase 0)
  29. Eligibility criteria
  30. Enrollment
  31. Exclusion criteria
  32. Expanded access
  33. Expanded access status
  34. Expanded access type
  35. Experimental arm
  36. Extension request
  37. Factorial assignment
  38. FDAAA 801 Violations
  39. First posted
  40. First submitted
  41. First submitted that met QC criteria
  42. Food and Drug Administration Amendments Act of 2007, Section 801 (FDAAA 801)
  43. Funder type
  44. Gender-based eligibility
  45. Group/cohort
  46. Human subjects protection review board
  47. Inclusion criteria
  48. Informed consent
  49. Informed consent form (ICF)
  50. Intervention model
  51. Intervention/treatment
  52. Interventional study (clinical trial)
  53. Investigator
  54. Last update posted
  55. Listed location countries
  56. Location terms
  57. Masking
  58. NCT number
  59. No intervention arm
  60. Observational study
  61. Observational study model
  62. Other adverse event
  63. Other study IDs
  64. Other terms
  65. Outcome measure
  66. Parallel assignment
  67. Participant flow
  68. Patient registry
  69. Phase
    1. Phase 1
    2. Phase 2
    3. Phase 3
    4. Phase 4
  70. Phase Not Applicable
  71. Placebo
  72. Placebo comparator arm
  73. Primary completion date
  74. Primary outcome measure
  75. Primary purpose
  76. Principal investigator (PI)
  77. Protocol
  78. Quality control (QC) review
  79. Randomized allocation
  80. Recruitment status
    1. Not yet recruiting
    2. Recruiting
    3. Enrolling by invitation
    4. Active, not recruiting
    5. Suspended
    6. Terminated
    7. Completed
    8. Withdrawn
    9. Unknown
    10. Withheld (?)
  81. Registration
  82. Removed location countries
  83. Reporting group
  84. Responsible party
  85. Results database
  86. Results delayed
  87. Results first posted
  88. Results first submitted
  89. Results first submitted that met QC criteria
  90. Results returned after quality control review
  91. Results submitted to ClinicalTrials.gov
  92. Secondary outcome measure
  93. Serious adverse event
  94. Sex
  95. Sham comparator arm
  96. Single group assignment
  97. Sort studies by
  98. Sponsor
  99. State
  100. Statistical analysis plan
  101. Status
  102. Study completion date
  103. Study design
  104. Study documents
  105. Study IDs
  106. Study record
  107. Study registry
  108. Study results
  109. Study start date
  110. Study type study type (Q78088984)
  111. Submitted date
  112. Title title (Q783521)
  113. Title acronym
  114. U.S. Agency for Healthcare Research and Quality United States Agency for Healthcare Research and Quality (Q4692008)
  115. U.S. Food and Drug Administration
  116. Unknown

See also[edit]