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.
The CRPS Registry was set up in 2008. It now holds over 600 records and has contributed to eleven 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 - please note our new address
One of our Network members has recently established a new website for the CRPS Forum, which is aimed at providing support for people with CRPS and their healthcare providers. Features include a CRPS screening tool for use in an outpatient setting, posters and leaflets. More information can be found at http://crpsforumcork.com, or you can watch their "Keep Moving, Keep Using" hand exercise video below:
(Site updated 24/01/2020)