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Clinical trials of vaccines and drugsInterpreting results of clinical trials

Clinical trials of vaccines and drugs are carried out to show that they are safe and effective. Tests are randomised, use control groups given placebos, and are carried out double-blind to avoid bias.

Part of Human BiologyNeurobiology and immunology

Interpreting results of clinical trials

When interpreting results following clinical trials, researchers must ensure that the subject groups are of a suitable size to reduce the magnitude of experimental error.

A small subject group increases the chance that an unknown factor could affect the result. It is less likely to pick up on variation between individuals. The subject groups need to be of a large enough size in order to have some relevance when applying the data to the wider population.

It is important that subject groups have sufficient diversity so that the results of the trial reflect the population and avoid bias. Care needs to be taken to properly reflect age, gender, ethnicity, class, and geographic spread.

The results from all groups are then compared to determine if there are any statistically significant differences between the results.

When the results of clinical trials are displayed as a graph, they often feature error bars that can help show the spread of data around the mean value. A small error bar means a smaller from the mean value. Larger bars mean that there is a wider spread of data from the mean value.

A bar graph showing an example of a clinical trial using phosphate, oxalate and uric acid.