If you take part in a clinical trial you may be one of the first people to benefit from a new treatment. It may turn out to be no better, or to be worse, than the standard treatment.
Many people choose to take part in clinical trials because it helps researchers to understand more about a particular disease or condition, which may benefit them or others like them in the future.
Finding out about clinical trials
If you are ill and interested in taking part in a clinical trial, your doctor or other health professionals may know of research going on that may be right for you. Few health professionals know of all the trials going on in their clinical area. There could be dozens or even hundreds.
Searching the registers
You can look for information on the registers of clinical trials, such as the World Health Organization (WHO) International Clinical Registry Platform. This collects information from different registers but it is currently designed for use by scientists and funders of clinical trials and is not easy for members of the public to use.
You can also find out about research studies registered in the UK at the UK Clinical Trials Gateway (external link)
You will probably need to talk to your doctor or specialist nurse about any information on trials that you have found in the registers.
For some conditions, you can find out about trials from patient organisations. CancerHelp (the patient information arm of Cancer Research UK) has clear information on nearly all the cancer clinical trials happening in the UK.
Other health charities also have user-friendly information about some clinical trials. Charities that are not listed may not formally publish lists of clinical trials but may know of some that are relevant to particular conditions.
Questions to ask
When you express interest in a trial, a doctor or nurse is likely to tell you something about it in person. You will also be given some information to take away.
You may come back with some questions that you feel have not been answered.
The UK Clinical Research Collaboration is a partnership of organisations that are establishing the UK as a world leader in clinical research. It suggests a number of general and practical questions you may want to ask:
- What is the aim of the trial and how will it help people?
- Who is funding the trial?
- What treatment will I get if I do not take part in the trial?
- How long is the trial expected to last and how long will I have to take part?
- How long will it be before the results of the trial are known?
- What will happen if I stop the trial treatment or leave the trial before it ends?
- How much of my time will be needed?
- What extra tests or appointments will I have?
- Will I need to take time off work?
- Will I need extra help from family or friends?
- Will you cover the costs of my travel to take part in the trial?
- If the trial is testing a new drug, will I have to collect it from the hospital, will it be sent to me by post, or will I get it through my doctor?
- Will I have to keep a questionnaire or keep a diary?
- What are the possible side effects of my treatment?
- How may the treatments affect me physically and emotionally?
- Who can I contact if I have a problem? Will someone be available 24 hours a day?
- How do I find out the results of the trial?
Advantages of being in a clinical trial
The main reason for carrying out trials is to determine whether a new treatment is more effective than previous ones. So an advantage of being involved in a trial is that you may be given a new treatment that is better for your condition.
During the trial your treatment and progress may be monitored more closely than if you were receiving the standard treatment.
After completion of the trial, health professionals will be able to offer you the most appropriate and effective treatment for you.
Trials are very important in helping to find the best possible treatments. By being involved in a trial, you will obtain information and evidence that may be helpful to you in the future, as well as helping the NHS to give people the best possible standard of care.
Disadvantages of being in a clinical trial
The disadvantages are:
- You cannot be sure of the outcome.
- You may be given a new treatment that is not as effective as the standard treatment.
- It is possible that you will experience unexpected side effects.
- You may have to visit your place of treatment more often, or have more tests, treatments or monitoring than you would if you were receiving the standard treatment.
You cannot be entered into a trial if you don't want to be. If you're asked to take part, you're free to say yes or no at any time. For children and those under 18, a parent or guardian has to give permission.
The doctor organising your treatment will usually talk to you about being involved. They should explain the possible risks and benefits.
Make sure you are happy with the trial and have been given all the information you want before you give your consent. This may mean taking some time to think about it and talk it over with family or friends, unless a decision is needed urgently because of your medical condition. You should be given the time to do this.
If you do decide to take part, you will be asked to sign a form to say that you are agreeing to take part in a trial and have understood what that will involve. This is called giving your informed consent.
Sometimes it is not possible for you to be involved in a particular trial.
Before you join a trial, you may need to have tests to see if you can take part. You may have to be tested to see if you have raised levels of a particular hormone.
This will allow the researchers to know more about your health before you start treatment, so at the end of the trial they can tell if there's been improvement.
During the trial, you may have more tests to see whether the treatment is working. It may be possible for the tests to be carried out as part of your routine care, or you may have to make more visits than usual to your GP or hospital clinic.
Leaving a trial
You may decide to stop taking part in a trial if your condition is getting worse or if you feel the treatment is not helping you. You can also choose to leave at any point without giving a reason, and without it affecting the care you receive.
If there are signs that the treatment in a trial could be unsafe, the research team or the regulators will stop the trial.
Last updated: 04 October 2011
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