Clinical Trials
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What is a clinical trial?
Clinical trials are research studies in which people volunteer to help find answers to specific health questions. When carefully conducted, they are the safest and fastest way to find new treatments and ways to improve health.
Clinical trials are conducted according to a plan, called a protocol, which describes:
- the types of patients who may enter the study
- the schedules of tests and procedures
- the drugs involved
- the dosages, or amount of the drug
- the length of the study
- what the researchers hope to learn from the study.
Why are clinical trials done?
Clinical trials are conducted for many reasons:
to determine whether a new drug or device is safe and effective for people to use.
to study different ways to use standard treatments or current, approved treatments so that they will be more effective, easier to use, or decrease certain side effects.
to learn how to safely use a treatment in a population for which the treatment was not previously tested, such as children.
Searching for clinical trials
This website initially provides limited information on individual clinical trials in the European Union and European Economic Area. It will gradually contain more information as clinical trial sponsors and regulators use it to initiate and oversee clinical trials since the launch of this website and the database underpinning this website, on 26 January 2022.
Clinical trials with a decision issued after mid-August 2022 that have deferrals of any type in the application form are currently not published on CTIS. This is a temporary measure until the functionalities of the public portal are fully restored.
Information on individual clinical trials initiated in the European Union and the European Economic Area before 26 January 2022 can be found in the European Union Clinical Trials Register.
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