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The Specific Characteristics of a Clinical Trial
Understanding what it means to participate in a clinical trial, knowing your rights, and having the information you need to make an informed decision.
Why might you be invited to participate in a clinical trial?
During your treatment, your doctor may offer you the opportunity to participate in a clinical trial involving an innovative diagnostic method, treatment strategy, medication, health product, or medical device.
The goal is to advance medical knowledge and improve cancer care.
Key Takeaways
Participating in a clinical trial is an option, never an obligation. Your decision will not affect the quality of your care at Gustave Roussy.
A Free and Informed Decision
The doctor will explain the purpose of the study, how it will be conducted, any potential limitations, the expected benefits, the identified risks, and other treatment options.
You can take as much time as you need to read the documents provided, discuss them with your family and friends, and ask any questions you may have before giving your answer.
If you agree to participate, you will be asked to sign an informed consent form. You will receive a copy.
You may withdraw from the program at any time, without having to provide a reason and without any impact on the quality of your care.
Your questions are essential
Before making your decision, you might want to ask:
- What is the purpose of the study?
- Why am I being offered this trial?
- What additional tests or consultations are planned?
- What are the expected benefits and known risks?
- What other treatment options are available?
- Who should I contact if I have a question during the trial?
- What happens if I want to stop participating?
Diagnostic and Therapeutic Tests
Studies can also evaluate diagnostic procedures, management strategies, or the effects of treatments. They help us better understand the disease and improve clinical practices.
What information may be collected?
Depending on the study’s objective, the information collected may relate to your administrative status, your medical history, your diagnostic and therapeutic care, and certain aspects of your lifestyle.
When the research requires the collection of particularly sensitive data, you will be provided with specific information, and your consent will be obtained in accordance with the procedures established for the study.
Protection of Information
Access to information used for research is strictly regulated. The procedures for collecting and using your information, as well as how to exercise your rights, must be explained in the informational documents provided for the study.