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ACTIVE NOT RECRUITING
NCT05782972
PHASE4

Therapeutic Response of Sodium-glucose Co-transporter Type-2 Inhibitor in Non-diabetic MAFLD Patients: a Pilot Study

Sponsor: Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation

View on ClinicalTrials.gov

Summary

The goal of this single arm, prospective study is to test the therapeutic response of oral dapagliflozin (Forxiga) 10 mg/day for 24 weeks in non-diabetic MAFLD patients. The primary outcomes are the improvement of liver inflammation or fibrosis parameters after 24 weeks treatment. The adverse events were also recorded.

Key Details

Gender

All

Age Range

20 Years - Any

Study Type

INTERVENTIONAL

Enrollment

50

Start Date

2023-03-11

Completion Date

2025-12-31

Last Updated

2025-03-03

Healthy Volunteers

No

Interventions

DRUG

dapagliflozin (Forxiga)

The participants received oral dapagliflozin (Forxiga) 10 mg/day for 24 weeks.

Locations (1)

Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation

New Taipei City, Taiwan