Cookies on this website
We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.
Skip to main content

The National Registry of Rare Kidney Diseases (RaDaR) is a research initiative by UK kidney specialist (the Renal Association and the UK Renal Registry). It is designed to gather information from patients with rare kidney disease and in particular women with chronic kidney disease (CKD). The group aims to look into how women with CKD cope with pregnancy and what can be done to improve care.

FULL TITLE

 Kidney disease and pregnancy. 

OVERVIEW

 National Registry of Rare Kidney Diseases (RaDaR) 

WHO CAN PARTICIPATE IN THIS STUDY? 

Women with chronic kidney disease who have, or have had, a pregnancy.

ABOUT THE STUDY 

The National Registry of Rare Kidney Diseases (RaDaR) is a research initiative by UK kidney specialist (the Renal Association and the UK Renal Registry). It is designed to gather information from patients with rare kidney disease and in particular women with chronic kidney disease (CKD). The group aims to look into how women with CKD cope with pregnancy and what can be done to improve care.

ETHICAL APPROVAL 

Ref number xxxxx

CONTACT US TO GET INVOLVED 

If you are interested in taking part, you can use our main contact form, or contact the team listed on this page.