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Study identifier: NCT07322237 Synced from ClinicalTrials.gov · July 29, 2026
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DICE Study- Diastolic Improvement With Carvedilol & Empagliflozin in Patients With Cirrhosis

Condition: Cirrhotic Cardiomyopathy · Empagliflozin · Cardiometabolic Risk Factors  ·  Sponsor: Post Graduate Institute of Medical Education and Research, Chandigarh

PhasePhase 4
Planned participants400
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

1. This proposed double-blind placebo controlled randomized controlled trial incorporates recent advances in management of heart failure and portal hypertension using the SGLT-2 inhibitor i.e. EMPAGLIFLOZIN. The drug has been found to be useful in large trials on heart failure with preserved ejection fraction in the general population with improvement in MASLD progression, with improvement in body weight and hepatic steatosis but no change in liver fibrosis. 2. Sodium-glucose cotransporter 2 (SGLT2) inhibitors have been shown to reduce the development and progression of heart failure in patients with type 2 diabetes and in those with heart failure and a reduced and preserved ejection fraction. In patients with cirrhosis safety of empagliflozin in a dose of 10 mg has been demonstrated. 3. Prevention of decompensation related events in cirrhosis is the key endpoint of any liver-directed therapy as the median survival in the compensated state exceeds 10 years but median survival in the decompensated state approximates 1.5 years. Previous data has demonstrated the risk of hepatic decompensation acute kidney injury and poor survival in patients with cirrhosis and heart failure with preserved ejection fraction (HFpEF) i.e. LVDD a large subset of whom meet criteria for CCM.

This description comes directly from the study's public registry record.

Talk to the study team

Madhumita Premkumar, MD DM  ·  01722754777  ·  drmadhumitap@gmail.com

Madumita Premkumar  ·  01722754777

Always discuss trial participation with your own doctor first.

Locations (1)

PGIMER ChandigarhChandigarh, IndiaRecruiting

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Source record: clinicaltrials.gov/study/NCT07322237