Status:
NOT_YET_RECRUITING
Advanced Fibrosis Detection for MASLD in Primary Care
Lead Sponsor:
Medical University of South Carolina
Collaborating Sponsors:
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
National Institutes of Health (NIH)
Conditions:
Metabolic Dysfunction-associated Steatotic Liver Disease
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
This proposal evaluates the implementation of a novel, non-interruptive, electronic health record alert for metabolic dysfunction-associated steatotic liver disease (MASLD) fibrosis risk assessment in...
Detailed Description
Metabolic dysfunction-associated steatotic liver disease (MASLD, formerly nonalcoholic fatty liver disease \[NAFLD\]) affects an estimated 1in 3 persons in the U.S., a prevalence expected to increase ...
Eligibility Criteria
Inclusion
- Patients
- Patients with a diagnosis code for MASLD
- Type 2 diabetes mellitus will
Exclusion
- All patients with cirrhosis, complications of cirrhosis (e.g. portal hypertension, hepatic encephalopathy), hepatocellular carcinoma, or previous liver transplant will be excluded.
- pregnant women.
- Clinicians Clinicians will also be study participants, as we will be surveying them for feedback on the MASLD fibrosis risk assessment intervention. The MUSC primary care network at last count employed 122 clinicians across the 27 primary care practices.
- Inclusion criteria:
- 1\. All physicians, physician assistants, and nurse practitioners delivering primary care during the intervention phase of the study.
- Exclusion criteria:
- None
Key Trial Info
Start Date :
December 1 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
September 1 2030
Estimated Enrollment :
225 Patients enrolled
Trial Details
Trial ID
NCT07159386
Start Date
December 1 2025
End Date
September 1 2030
Last Update
October 6 2025
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