Clinical Trials
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Welcome - Adults
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What are Phase 1 clinical trials?
What are Phase 2 clinical trials?
What are Phase 3 clinical trials?
What does “post marketing surveillance” – also known as Phase 4 trials – mean?
What is a “placebo”?
Who is allowed to set up a clinical trial?
Who regulates clinical trials?
When and how is a trial approved?
What is an “informed consent”?
What will I find in an informed consent document?
What are “eligibility criteria”?
What are “inclusion criteria”?
What are “exclusion criteria”?
What does “blinding” mean?
What does “bias” mean?
What are “randomised” trials?
What is an “open label” trial?
What are the different types of clinical trials that I can participate in?
How can I find out which clinical trials are going on?
How can I volunteer and participate in a clinical trial?
Can I contact a company directly to volunteer in a clinical trial?
Will I be compensated or paid for participating in a clinical trial?
Why should I participate in a clinical trial?
What questions should I ask before volunteering?
What will happen to me during a clinical trial?
My physician won’t put my name forward. What should I do?
Will taking part in a clinical trial affect the care I receive from my doctors?
Who decides whether elderly, incapacitated or children participate in a clinical trial?
Will I have to stop taking my current medication? What are the risks and benefits of participating in a clinical trial?
Can I withdraw from a trial?
Will taking part in a clinical trial adversely affect the care I receive from my doctor?
Will I find out the results?
What will happen to my samples or information about me during and after the trial? Will others be able to look at it or use it for further research?
Is there someone I can ask if I have questions or problems that arise while I am in the trial?
If the treatment works, will I be able to carry on getting it after the trial has ended?
What is the Declaration of Helsinki?
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