ProtocolDeviationPlaceboParallelStudyPhaseIPhaseIVMulticenterTrialAuditTrailFollow-up VisitClinicalEndpointBlindingControlGroupProtocolPilotStudyRegulatoryAuthorityDataLockCaseReportForm(CRF)PatientRecruitmentDouble-BlindStudyStandardOperatingProcedure(SOP)EligibilityCriteriaInvestigatorMeetingPrincipalInvestigatorTrialMonitorScreeningVisitTrialRegistryInstitutionalReviewBoard(IRB)RandomizationOpen-LabelTrialInterventionData SafetyMonitoringBoard(DSMB)SafetyProfilePhaseIIDataManagementGoodClinicalPractice(GCP)AdverseEventSponsorCrossoverStudySurrogateEndpointSourceDataVerificationClinicalStudyReport(CSR)EthicsCommitteeEndpointClinicalResearchCoordinatorDropoutRatePhaseIIIEfficacyAdaptiveDesignInformedConsentRecruitmentTargetStatisticalAnalysisPlan(SAP)ProtocolDeviationPlaceboParallelStudyPhaseIPhaseIVMulticenterTrialAuditTrailFollow-up VisitClinicalEndpointBlindingControlGroupProtocolPilotStudyRegulatoryAuthorityDataLockCaseReportForm(CRF)PatientRecruitmentDouble-BlindStudyStandardOperatingProcedure(SOP)EligibilityCriteriaInvestigatorMeetingPrincipalInvestigatorTrialMonitorScreeningVisitTrialRegistryInstitutionalReviewBoard(IRB)RandomizationOpen-LabelTrialInterventionData SafetyMonitoringBoard(DSMB)SafetyProfilePhaseIIDataManagementGoodClinicalPractice(GCP)AdverseEventSponsorCrossoverStudySurrogateEndpointSourceDataVerificationClinicalStudyReport(CSR)EthicsCommitteeEndpointClinicalResearchCoordinatorDropoutRatePhaseIIIEfficacyAdaptiveDesignInformedConsentRecruitmentTargetStatisticalAnalysisPlan(SAP)

Clinical Trials Bingo - Call List

(Print) Use this randomly generated list as your call list when playing the game. There is no need to say the BINGO column name. Place some kind of mark (like an X, a checkmark, a dot, tally mark, etc) on each cell as you announce it, to keep track. You can also cut out each item, place them in a bag and pull words from the bag.


1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
  1. Protocol Deviation
  2. Placebo
  3. Parallel Study
  4. Phase I
  5. Phase IV
  6. Multicenter Trial
  7. Audit Trail
  8. Follow-up Visit
  9. Clinical Endpoint
  10. Blinding
  11. Control Group
  12. Protocol
  13. Pilot Study
  14. Regulatory Authority
  15. Data Lock
  16. Case Report Form (CRF)
  17. Patient Recruitment
  18. Double-Blind Study
  19. Standard Operating Procedure (SOP)
  20. Eligibility Criteria
  21. Investigator Meeting
  22. Principal Investigator
  23. Trial Monitor
  24. Screening Visit
  25. Trial Registry
  26. Institutional Review Board (IRB)
  27. Randomization
  28. Open-Label Trial
  29. Intervention
  30. Data Safety Monitoring Board (DSMB)
  31. Safety Profile
  32. Phase II
  33. Data Management
  34. Good Clinical Practice (GCP)
  35. Adverse Event
  36. Sponsor
  37. Crossover Study
  38. Surrogate Endpoint
  39. Source Data Verification
  40. Clinical Study Report (CSR)
  41. Ethics Committee
  42. Endpoint
  43. Clinical Research Coordinator
  44. Dropout Rate
  45. Phase III
  46. Efficacy
  47. Adaptive Design
  48. Informed Consent
  49. Recruitment Target
  50. Statistical Analysis Plan (SAP)