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The molecular investigation of unexplained anaemias and related congenital anaemias

Contact phone number: Dr Peter Carey/Dr Jonathan Wallis 0191 2824743

Why is this study important? 

Some rare types of anaemia (lack of blood) are inherited (passed from parent to child in genes). Some causes are known, while others are waiting to be discovered.

What is the aim of this study? 

The aim is to find the genes that cause these anaemias. This could help to diagnose patients more quickly and find new treatments.

What do people in this study have to do? 

The study is for patients who have anaemia for which no cause has been found. Checks for faulty genes would be done from blood or saliva. If you have had a bone marrow test done, we will ask if we may have any left over samples. We would collect relevant information about your anaemia from your medical notes.

What are the risks and benefits for participants? 

It is possible we could stumble upon a faulty gene, unrelated to anaemia, which could affect your health. You can choose whether you would want to know about this. You will not be recognisable in any document published by us.  You will be able to tell us whether you want any information on the results of our research by ticking a box on the following consent form.

For further information about this study please follow link

http://public.ukcrn.org.uk/search/StudyDetail.aspx?StudyID=16847

Recruitment to this study is due to end:

Nov 2018

A summary of the study findings should be available by:

We hope to publish our research results in a scientific journal, readable by physicians around the world.

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Select a trial from the list below to find out more about what it’s all about and how you can get involved in helping others.

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The information from this study may help us to increase our understanding and improve future treatment for patients with TTP.

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The study is for patients who have anaemia for which no cause has been found.

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