June 7, 2004Evaluation Of Randomised Controlled Trials
M. J. McKeown, MD, FACOG, FACS
Objective and Ethics
Outcome Measures
Interventions
Study Population And Sample Size
Checklist For Appraising Randomized Trials
Objective and Ethics
Back to the Table of Contents
- Objective:
- What is it that makes the purpose of this study relevant?
- Ethics:
- Has the study satisfied all review boards for ethics?
Outcome Measures
Back to the Table of Contents- The primary outcome measures should be:
- 1. easy to diagnose or observe
2. free of measurement errors or ascertainment errors
3. capable of being observed independent of treatment assignment
4. clinically relevant
5. chosen before the start of data collectionInterventions
Back to the Table of Contents- The test and control treatment must be:
- 1. distinguishable from one another
2. medically justifiable
3. compatible with the health care needs of the subjects
4. acceptable to the patients and their care providers
5. there must be reasonable doubt about the efficacy of the treatment
6. it should be thought the benefits of the treatment will outweigh the risksStudy Population And Sample Size
Back to the Table of Contents- Define the exclusion and inclusion criteria and how the subjects should be sampled.
Decide how many subjects will be needed in the trialChecklist For Appraising Randomized Trials
Back to the Table of Contents- 1. Was the objective of the trial appropriately described?
2. Was a satisfactory statement given of the entry criteria to the trial.
3. Were concurrent controls used?
4. Were the treatments well defined?
5. Was random allocation to treatments used?
6. Was the potential degree of blindness used?
7. Was there a satisfactory description of outcome criteria?
8. Were the outcomes measured appropriate?
9. Was a pre-study calculation of sample size needed reported?
10. Was the duration of the post-treatment follow-up stated?
11. Were the treatment and control groups comparable?
12. Were a high proportion of the subjects followed up?
13. Were the drop-outs described by treatment and control groups?
14. Were the side-effects of treatment reported?
15. How were the ethical issues dealt with?
16. Was there a statement adequately describing the statistical procedures used?
17. What tests were used to compare the outcome in test and control patients?
18. Were 95% confidence intervals given for the main result?
19. Were additional analyses done to see whether baseline prognostic factors influenced the outcomes observed?
20. Were the conclusions drawn from the statistical analyses justified?