Nanfang Hospital of Southern Medical University
Guangzhou, Guangdong, 510515, China
NCT Number: NCT03723252
This is a multicentre, randomized, placebo-controlled trial to assess the efficacy and safety of dapagliflozin on improving non-alcoholic steatohepatitis as determined by liver biopsies and metabolic risk factors.
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Notify Me18 year and older
All sexes
Interventional
Phase 3
Guangzhou, Guangdong, 510515, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will receive dapagliflozin 10mg po qd
Participants will receive placebo po qd
Time frame: Baseline to 12 months
Time frame: Baseline to 12 months
defined as a hepatocellular ballooning score of 0, and lobular inflammation score of 0 or 1) without worsening of fibrosis
Time frame: Baseline to 12 months
defined as reduction in fibrosis of at least 1 stage) without worsening of NASH
Time frame: Baseline to 12 months
Time frame: Baseline to 12 months
Time frame: Baseline to 12 months
Time frame: Baseline to 12 months
Time frame: Baseline to 12 months
Time frame: Baseline to 12 months
Time frame: Baseline to 12 months
Time frame: Baseline to 12 months
Time frame: Baseline to 12 months
Time frame: Baseline to 12 months
Time frame: Baseline to 12 months
Time frame: Baseline to 12 months
Nanfang Hospital, Southern Medical University
Other
Efficacy and Safety of Dapagliflozin in Non-alcoholic Steatohepatitis: a Multicentre, Randomized, Placebo-controlled Trial
Acronym: DEAN
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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