The CRPS UK Clinical & Research Network was established in 2006 and is a research collaboration between a number of UK NHS trusts and academic institutions with an interest in Complex Regional Pain Syndrome. A primary aim of the CRPS Network is to raise awareness and understanding of Complex Regional Pain Syndrome amongst health professionals, patients and the general public. We maintain a national CRPS Registry database as part of a long-term research study.
2018 was the 10th anniversary year of the CRPS Registry, which now holds 584 records and has contributed to nine different national and international research studies.
Our website offers a variety of information and resources, including:
- Details about the Registry and how to become a recruiting centre
- Summaries of our research and how to apply to access Registry data for your studies
- Links to our research publications
- Copies of our newsletters
- A downloadable resource library of leaflets, guidance and other useful links
- Frequently Asked Questions for patients
- How to get in touch with us
(Site updated 13/08/2019)