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The Complex Regional Pain Syndrome (CRPS) and Chronic Pain Research Study Trials Tracker was designed to bring together details of any CRPS and chronic pain trials currently recruiting in the UK. This will enable you to find RCT clinical trials and research studies that you might be eligible to take part, both local to you or further afield.
If you have any questions about taking part in research studies or clinical trials, you can contact us or get in touch with the clinical trial or research study team directly (contact details are included in the opportunity's listing).
If you are a researcher and you would like to include your research study or clinical trial, please send the details by email.
The aim of this study is to gain an understanding of the treatment priorities and preferences of CRPS patients and therapists regarding conservative treatments. It is open to patients who have been diagnosed with CRPS and therapists who treat CRPS patients.
A study from a team of neuroscientists at the University of Cambridge who are developing a new Minimally Invasive Spinal Cord Stimulator (MI-SCS), looking to recruit an advisory group of 6-8 people with lived experience of chronic neuropathic pain to work with the research team.
Trial participants required for a research study into the treatment of Phantom Limb Pain (PLP).
Do you experience Phantom Limb Pain (PLP)? Are you over 18 and live in the UK? Do you experience PLP at least 2 days a week, and rate that pain as more than 4 on 0-10 Scale? If you do, you are invited to find out more about taking part in this research study.
This study is looking to test how different emotional or cognitive variable (such as stress, brain fog, etc.) influence whether patients with CRPS will get worse in the near future. The study is looking for adult patients with Complex Regional Pain Syndrome and can be conducted remotely at the patients' home.
This study aims to develop clinical recommendations that will expecite patient access to therapy-led treatment across the CRPS care pathway. Participation will involve an online workshop to discuss experiences of therapies received and any changes noticed as a result of receiving this care.
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