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Clinical Trial Summary

The study is stratified cluster randomized trial. The study population will include adults with T2D and presumed NASH.


Clinical Trial Description

The study is a multi-centered, stratified cluster randomized controlled, open-labeled two-phase study. Clusters will be independent LMC clinic sites with patients as participants. The use of the stratified cluster randomization design will help prevent the potential for cross-contamination of screening methods. Study participants who meet eligibility criteria undergo NASH screening. Everything, other than routineness of screening, is maintained the same in both the groups. The screening intervention received is determined by the site of the participant's provider. All participants enrolled will undergo biochemical screening. Regardless of randomization, any participants meeting biochemical cut-offs (FIB-4 index ≥1.3 or NFS >-1.455) will undergo FibroScans. Clinical data and a health-related quality of life assessment will also be collected. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05029583
Study type Interventional
Source LMC Diabetes & Endocrinology Ltd.
Contact Lisa Chu, PhD
Phone 416-268-8787
Email lisa.chu@LMC.ca
Status Recruiting
Phase N/A
Start date August 11, 2021
Completion date October 5, 2025

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