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Recruiting

NCT Number: NCT07108075

Acute Portal Pressure Reduction by Metformin and Carvedilol Compared to Carvedilol Alone in Cirrhosis.

Clinically significant portal hypertension (CSPH) is defined as HVPG >10 mmHg. Patients with CSPH are at risk of developing esophageal varices and clinical decompensation (variceal bleeding, ascites, jaundice, encephalopathy), which mark the transition from compensated stage to a stage of the disease (decompensated) associated with higher mortality (1). HVPG is calculated by subtracting the free hepatic venous pressure (FHVP), a measure of systemic pressure, from the wedged hepatic venous pressure (WHVP), a measure of hepatic sinusoidal pressure. HVPG is surrogate marker in many clinical applications such as gold standard test to evaluate presence and severity of portal hypertension (PHT) diagnosis, risk stratification, monitoring of the patients on beta blockers (2). Non selective beta-blockers like propranolol and carvedilol are indicated in adults for primary and secondary prophylaxis of variceal hemorrhage. Acute hemodynamic response to intravenous propranolol with HVPG values coming down to <12 mm Hg or reduction to >20% from baseline have been shown to be associated with reduced long term risk of variceal bleed. Metformin has also recently showed to reduce portal pressure in a randomised control study. The mechanism of action of metformin is different from beta blockers (by increasing nitric oxide by upregulating iNOS and eNOS). Hence we are planning the current work to evaluate Acute portal pressure reduction by Metformin and Carvedilol compared to Carvedilol alone in cirrhosis - a randomised, double blind study.

Recruiting

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Institute of Liver & Biliary Sciences (ILBS)

New Delhi, National Capital Territory of Delhi, 110070, India

Location status: Recruiting

Location contact

Garvit Mundra, MD

CONTACT

[email protected]

01146300000

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Consecutive patients of cirrhosis with variceal bleed.

Exclusion criteria

  • Age < 18 and > 75yr,
  • CTP Score ≥12,
  • Patients of cirrhosis without variceal bleed,
  • Patients on metformin, nonselective β-blockers or carvedilol treatment within last 5 days,
  • S.Bilirubin > 3 mg/dl,
  • S.creatinine 1.5 mg/dl,
  • Contraindications to NSBB (heart rate < 60 /min, BP < 110/60 mm Hg,
  • Asthma, heart failure),
  • PVT,
  • HCC
  • HE grades 2-4

Treatment and study plan

Carvedilol

Drug

Carvedilol 12. 5mg

metformin

Drug

Metformin 1000 mg

Primary outcomes

  1. HVPG response (decrease by ≥ 20 % from baseline or < 12 mmHg).

    Time frame: 2 hours

Secondary outcomes

  1. HVPG decrease by ≥ 10% in both groups.

    Time frame: 2 hours

  2. Reduction in HVPG in both groups.

    Time frame: 2 hours

  3. Change in blood sugar level after 2 hours of the drug in both groups.

    Time frame: 2 hours

  4. Change in inflammatory markers (IL-10, TNF α, i-NOS, e-NOS) in both groups.

    Time frame: 2 hours

  5. Change in liver and spleen stiffness.

    Time frame: 2 hours

  6. Change in cardiac output in both groups.

    Time frame: 2 hours

Study contacts

Contact information is provided by the study sponsor or research team.

Dr Chitranshu Vashishtha, DM

CONTACT

[email protected]

01146300000

Dr Garvit Mundra, MD

CONTACT

[email protected]

01146300000

Sponsors and collaborators

Lead sponsor

Institute of Liver and Biliary Sciences, India

Other

Registry information

Official study title

Acute Portal Pressure Reduction by Metformin and Carvedilol Compared to Carvedilol Alone in Cirrhosis - a Randomised, Double Blind Study.

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Aug 6, 2025
Registry last updated
Aug 6, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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