The COherence of Scatter Identification and Exclusion Algorithm Study
Non-alcoholic fatty liver disease (NAFLD) is currently the most common liver condition worldwide; approximately 55% of the world population will have NAFLD by 2040. NAFLD is an unwanted side effect of common cancer therapies, such as chemotherapy. Ultrasound can detect NAFLD via measurement of the backscatter coefficie
| Condition(s) | Steatohepatitis, Nonalcoholic |
|---|---|
| Status | Recruiting |
| Study type | Observational |
| Summary | Non-alcoholic fatty liver disease (NAFLD) is currently the most common liver condition worldwide; approximately 55% of the world population will have NAFLD by 2040. NAFLD is an unwanted side effect of common cancer therapies, such as chemotherapy. Ultrasound can detect NAFLD via measurement of the backscatter coefficient (BSC). It is an attractive technique because of its low cost and availability, potentially enabling earlier detection of NAFLD in a larger population through screening. This approach has shown promise in detecting NAFLD but is limited by variability in measurement due to several factors. Measurement of the BSC requires assumptions about the nature of the tissue being measured; if these assumptions are incorrect, they can lead to inaccurate BSC measurements. To improve accu |
| Who can participate | Inclusion Criteria: Healthy Volunteers: * Healthy male or female adults (18 or above). * Volunteers must consider themselves fit and healthy. * RMH and/or ICR employees. Patients: * Patients undergoing liver MRI as part of clinical standard of care with evidence of steatosis on preceding MRI. * Aged 18 and above. Exclusion Criteria: Healthy Volunteers: * Volunteers that are under investigation or planning to consult their GP to seek investigation for an undiagnosed condition, particularly regarding pelvic or abdominal disease or injury. * Healthy volunteers who do not have an NHS number or who are not registered with a GP will be excluded. Patients: • Severe liver fibrosis (fibrosis stage F4) or severe cirrhosis. |
| Ages | 18 Years |
| Sex | All |
| Accepts healthy volunteers | Yes |
| Lead sponsor | Institute of Cancer Research, United Kingdom |
| Locations | London, Greater London, United Kingdom |
| Start date | 2024-08-27 |
| NCT ID | NCT06975579 |
| Official listing | https://clinicaltrials.gov/study/NCT06975579 |