Understanding how a wrist fracture heals and why some people develop long-lasting pain
Official title: PERCIPIENT - An Evaluation of Pain Biomarkers and Body Representation Outcomes After Distal Radius Fracture
Run by Cambridge University Hospitals NHS Foundation Trust · NCT07777081 · Data updated 2026-11-12
This study tests whether genetic markers, blood signals, heart-rate patterns, and brain body maps can predict which patients will have persistent pain after a distal radius fracture.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 200 (estimated) |
| Sponsor | Cambridge University Hospitals NHS Foundation Trust Academic / other |
| Locations | 1 site (Cambridge, Cambridgeshire) |
| Status | Recruiting |
| Started | August 12, 2026 |
| Main results expected | August 12, 2031 |
| Study ends | August 12, 2032 |
| Registry record updated | August 20, 2026 |
| Trial ID | NCT07777081 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18 years and older with a distal radius fracture within the past 6 weeks or individuals with chronic CRPS who can consent and comply with study procedures.
✕Probably not a fit
Patients unlikely to benefit are those unable to complete consent processes, with multiple traumas or significant neurological disorders that preclude participation, or with conditions that interfere with study measurements.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational cohort follows adults with recent distal radius fractures and a smaller group with chronic CRPS to explore biological and neurophysiological factors that influence recovery. Researchers will collect genetic data, blood biomarkers, wearable autonomic signals, and functional MRI to study body representation in the brain after injury. The goal is to identify early indicators that distinguish those at risk for chronic pain and CRPS, enabling targeted support in the future. The study plans to recruit about 250 participants over four years across Cambridge-area sites. Analyses will focus on linking multi-domain phenotypes with long-term outcomes to generate new hypotheses about pain mechanisms.
Why it matters
Potential benefit: If successful, findings could lead to earlier identification of patients at risk for chronic pain and CRPS after a wrist fracture, potentially guiding personalized monitoring and interventions.
How similar studies have gone: Previous work in this area has shown promise linking biomarkers and brain mapping with pain trajectories, but this exact multi-domain approach in distal radius fracture recovery is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: Distal radius fracture (DRF) within past 6 weeks 18 and older Willing and competent to complete the informed consent process Exclusion Criteria: Inability to understand the informed consent process (Language, competence) Multiple trauma Significant neurological disease (multiple sclerosis, previous traumatic brain injury, previous stroke or cerebral haemorrhage and substantial tremor - including Parkinson's, significant resting tremor, or other aetiology) Amputation or medical confirmation of unilateral sensory deficit
Where it's running
-
Addenbrooke's Hospital
Cambridge, Cambridgeshire, United Kingdom Recruiting
Study contacts
- Study coordinator: Neal Chauhan, MBBS
- Email: neal.chauhan@nhs.net
- Phone: 01223 216182
Similar studies
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.