RecruitingPhase 4NCT07322237

DICE Study- Diastolic Improvement With Carvedilol & Empagliflozin in Patients With Cirrhosis

Empagliflozin + Carvedilol vs. Carvedilol Alone for Patients With Cirrhosis and Left Ventricular Diastolic Dysfunction and Impact on Hepatic Decompensation and Survival: A Double-Blind Placebo-Controlled Randomized Controlled Trial


Sponsor

Post Graduate Institute of Medical Education and Research, Chandigarh

Enrollment

400 participants

Start Date

Jan 1, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This study — called DICE — is testing whether a combination of two medications, carvedilol (a beta-blocker) and empagliflozin (originally a diabetes drug), can improve heart function in people with liver cirrhosis who also have a specific type of heart stiffness called diastolic dysfunction. **You may be eligible if...** - You are 18–65 years old - You have been diagnosed with liver cirrhosis - An echocardiogram (heart ultrasound) shows your heart muscle is stiff but still pumping normally (ejection fraction above 50%) **You may NOT be eligible if...** - Your kidneys are working poorly (creatinine above 2 mg/dL) - You had a urinary tract or genital infection in the last 3 months - You are taking a statin (cholesterol medication) currently - Your cirrhosis is very advanced (MELD score above 20) - You have coronary artery disease, a heart rhythm disorder, or a pacemaker - You have liver cancer or a liver shunt (TIPS procedure) - You are pregnant or breastfeeding - You are HIV positive - You have severe anemia - You had a serious bleed from your esophageal veins in the last 6 months Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGEmpagliflozin + Carvedilol

Patient Recruitment: The study participants are all cirrhosis patients receiving treatment at PGIMER Chandigarh. Eligible participants meeting LVDD criteria per the CCM Consortium 2020 consensus. Carvedilol Dosing protocol in this study Patients will be given carvedilol in a starting dose of 3.125 mg twice daily. The dose will be titrated weekly to achieve a target heart rate of 50-60/ min taking care that side effects such as hypotension bronchospasm excessive bradycardia are not seen. The maximum dosage allowed as per prior trial data is 25 mg per day. Empagliflozin Dosing protocol in this Study: • All patients will receive a standard dose of Empagliflozin fixed dose of 10 mg per day in patients with or without diabetes.

DRUGCarvedilol

* Carvedilol: Starting dose of 3.125 mg twice daily targeted upwards q 7 days to achieve target heart rate 10 mg placebo pill * Standard Medical Therapy


Locations(1)

PGIMER Chandigarh

Chandigarh, India

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NCT07322237


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