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Clinical Trials

How is trial data analysed/evaluated?

Data analysis is complex but may be used to show, for example, survival data. For clinical trials into potentially fatal diseases, eg cancer, the main evaluation of patient outcome is whether the patient dies or not, and the time from entry into the trial until death. Alternatively, patient outcome may be the time to some other measure of patient relapse, ie disease recurrence. According to the specific requirements of the trial protocol, both interim and final analysis may be carried out.

>>>> What are pharmacokinetic studies? >>>>

  1. Introduction
  2. What is a Clinical Trial?
  3. Clinical Trial procedure
  4. The role of the Chief Investigator
  5. The Protocol
  6. How is the size of a clinical trial determined?
  7. What is a multi-centre trial?
  8. Role of coordinating centre/Trials Unit
  9. What is randomisation?
  10. How is a patient randomised for a particular trial?
  11. What is a control in clinical trials?
  12. Forms and data management
  13. Statistics in clinical trials
  1. The role of the trial coordinator
  2. Follow up
  3. How is the trial data analysed/evaluated?
  4. What are pharmacokinetic studies?
  5. Ethical issues
  6. Conduct of Clinical Trials/Research
  7. What is a blind trial?
  8. Interpretation and publication of findings
  9. Survival Curves
  10. UKCCSG Protocols – development and approval process
  11. References
  12. Download PDF
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