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RECRUITING
NCT07285135
NA

Dietary Glycine Supplementation in Metabolic Dysfunction-associated Steatotic Liver Disease

Sponsor: Singapore General Hospital

View on ClinicalTrials.gov

Summary

This study aims to investigate abnormalities in glycine-dependent metabolic pathways in patients with metabolic dysfunction-associated steatotic liver disease (MASLD) and evaluate whether dietary glycine supplementation improves liver health and metabolic function. The study consists of two components. The first is a cross-sectional case-control study comparing urinary acylglycine concentrations and other glycine-dependent metabolic parameters between 60 participants with MASLD and 30 healthy controls. The second is a randomized, double-blind, placebo-controlled trial in which 60 participants with MASLD will receive either oral glycine supplementation (9 g/day) or placebo for 26 weeks. The primary outcomes are differences in urinary acylglycine concentrations between participants with MASLD and healthy controls, and changes in hepatic fat content measured by MRI-PDFF and urinary acylglycine concentrations following supplementation. Additional assessments will evaluate amino acid metabolism, glutathione metabolism, oxidative stress, inflammatory responses, and one-carbon metabolism-related biomarkers. Participants will undergo baseline, Week 12, and Week 26 assessments to evaluate metabolic changes and treatment responses.

Official title: Investigating the Effects of Dietary Glycine Supplementation in Patients With Metabolic Dysfunction-associated Steatotic Liver Disease

Key Details

Gender

All

Age Range

21 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

90

Start Date

2025-11-01

Completion Date

2029-01

Last Updated

2026-10-27

Healthy Volunteers

Yes

Interventions

DIETARY_SUPPLEMENT

Glycine

9g/day of glycine in capsules

DIETARY_SUPPLEMENT

Placebo

Microcrystalline cellulose in identifically-looking capsules

Locations (1)

Singapore General Hospital

Singapore, Singapore, Singapore