Latest Research in Ethics in Clinical Research

60 research papers · 2026 median publication year

Top Research Topics in Ethics in Clinical Research

Highest-Cited Papers

  1. Who Benefits From Medical Innovation? Global Representation, Affordability, Safety and Regulatory Equity in Alzheimer's Disease and Cancer Research
  2. Educational quality of YouTube cartoon videos on children’s tooth brushing: a cross-sectional content analysis
  3. Who Benefits From Medical Innovation? Global Representation, Affordability, Safety and Regulatory Equity in Alzheimer's Disease and Cancer Research
  4. Evidence-informed trial recruitment planning: an integrative review of infectious disease trials in Africa
  5. Rigorous, transparent and inconclusive: what Europe’s first joint clinical assessment reveals about a framework trying to serve everyone
  6. Regulatory and organisational barriers to non-commercial clinical trials in European nuclear medicine: Results from an EANM survey
  7. Perspectives on adverse events reporting in hybrid implementation science (IS) clinical trials of approved medications in Sub-Saharan Africa
  8. Rethinking rare: mitochondrial disease as a model for health system innovation and reform
  9. Dynamic Pooling and Regional Participation in Deceased-Donor Organ Allocation
  10. U.S. FDA REGULATORY GUIDELINES AND VALIDATION OF DIGITAL THERAPEUTICS
  11. Strategies to improve recruitment to randomised trials
  12. Indirect Estimation of the Number of Prevalent Cases – Relaxing the Steady State Assumption
  13. Demographic Classifications for Register Research: Syntax Documentation from the Insurance Medicine All Sweden (IMAS) Project.
  14. Projected Health Expenditures of Precision Medicine Under a Value-Based Pricing Framework
  15. Hemophilia care in the Netherlands: identification and visualization of the care pathway for young children with hemophilia
  16. Population Identity Preservation Prevents False Aggregation in Reanalysis of BACE1-Inhibitor Trials in Alzheimer's Disease
  17. Can discussions with patients and the public clarify missing data mechanisms for digital outcome measures?
  18. Demographic Classifications for Register Research: Syntax Documentation from the Insurance Medicine All Sweden (IMAS) Project.
  19. Policy Targeting with Binary Classification Trees: an Application to Rural Hospital Closures
  20. Forecasting Demand Under Limited Data: Benchmark Models for Workforce Capacity Planning in Translation Services
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L3 Region - - 2026 Sep Q3

Ethics in Clinical Research

60 papers

Top Topics (10)

Ethics in Clinical Research7
Health Systems, Economic Evaluations, Quality of Life5
Insurance, Mortality, Demography, Risk Management2
Hemophilia Treatment and Research2
Global Maternal and Child Health2
Carcinogens and Genotoxicity Assessment2
Health Literacy and Information Accessibility1
Health Policy Implementation Science1
Mitochondrial Function and Pathology1
Theoretical Economics1

Top Publications (20)

1.Who Benefits From Medical Innovation? Global Representation, Affordability, Safety and Regulatory Equity in Alzheimer's Disease and Cancer Research2.Educational quality of YouTube cartoon videos on children’s tooth brushing: a cross-sectional content analysis3.Who Benefits From Medical Innovation? Global Representation, Affordability, Safety and Regulatory Equity in Alzheimer's Disease and Cancer Research4.Evidence-informed trial recruitment planning: an integrative review of infectious disease trials in Africa5.Rigorous, transparent and inconclusive: what Europe’s first joint clinical assessment reveals about a framework trying to serve everyone6.Regulatory and organisational barriers to non-commercial clinical trials in European nuclear medicine: Results from an EANM survey7.Perspectives on adverse events reporting in hybrid implementation science (IS) clinical trials of approved medications in Sub-Saharan Africa8.Rethinking rare: mitochondrial disease as a model for health system innovation and reform9.Dynamic Pooling and Regional Participation in Deceased-Donor Organ Allocation10.U.S. FDA REGULATORY GUIDELINES AND VALIDATION OF DIGITAL THERAPEUTICS11.Strategies to improve recruitment to randomised trials12.Indirect Estimation of the Number of Prevalent Cases – Relaxing the Steady State Assumption13.Demographic Classifications for Register Research: Syntax Documentation from the Insurance Medicine All Sweden (IMAS) Project.14.Projected Health Expenditures of Precision Medicine Under a Value-Based Pricing Framework15.Hemophilia care in the Netherlands: identification and visualization of the care pathway for young children with hemophilia16.Population Identity Preservation Prevents False Aggregation in Reanalysis of BACE1-Inhibitor Trials in Alzheimer's Disease17.Can discussions with patients and the public clarify missing data mechanisms for digital outcome measures?18.Demographic Classifications for Register Research: Syntax Documentation from the Insurance Medicine All Sweden (IMAS) Project.19.Policy Targeting with Binary Classification Trees: an Application to Rural Hospital Closures20.Forecasting Demand Under Limited Data: Benchmark Models for Workforce Capacity Planning in Translation Services
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