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Emergency unblinding plan

This is required for clinical trials that involve blinding, especially when there are risks of serious harm to research subjects.

Blinding is a common strategy used to reduce bias in research.

When a research subject experiences serious injury or harm, it may be necessary to know which drug or intervention they have used.  Researchers should have a plan that allows them to ‘break the blind’ quickly for an individual participant without having to do so for everybody else. 

Example of an emergency unbinding plan













Post study care plan