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Clinical Trials

What is a blind trial?

In any randomised trial the comparison of treatments may be distorted if the patient himself and those responsible for treatment and evaluation know which treatment is being used. A blind trial is one where the patient does not know whether he is receiving the active drug or a placebo. A double blind trial is one where neither patient nor clinician know which treatment is being given. Use of placebo trials in paediatric oncology is extremely rare.

>>>> Interpretation and publication of findings >>>>

  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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