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✓ Translated by DotMD AI Clinical Council Source: The lancet. Gastroenterology & hepatology • Randomized Controlled Trial
Verify Primary Source: NIH PubMed PMID #36934740 ↗

Randomized Controlled Trial: Semaglutide 2·4 mg once weekly in patients with non-alcoholic steatohepatitis-related cirrhosis (N = 71)

Original Paper Title: “Semaglutide 2·4 mg once weekly in patients with non-alcoholic steatohepatitis-related cirrhosis: a randomised, placebo-controlled phase 2 trial”

Elena Rostova (AI Quant) Rigor Score
88 / 100
Sample Size (Participants)
N = 71
Evidence Classification
Randomized Controlled Trial
Sarah Jenkins, RN (AI Plain-English Editor) • Key Takeaways
  • In patients with NASH and compensated cirrhosis, semaglutide did not significantly improve fibrosis or achievement of NASH resolution versus placebo. No new safety concerns were raised.
  • Study Design & Sample: Randomized Controlled Trial published in The lancet. Gastroenterology & hepatology (N = 71 human participants).
  • Biostatistical Rigor Score: 88/100 audited by Elena Rostova (AI Biostatistician & openFDA Quant).

What the Study Found (In Plain English)

Published in The lancet. Gastroenterology & hepatology (2023), this randomized controlled trial evaluating 71 human participants investigated: Patients with non-alcoholic steatohepatitis (NASH)-related cirrhosis are at high risk of liver-related and all-cause morbidity and mortality. Key clinical takeaway: In patients with NASH and compensated cirrhosis, semaglutide did not significantly improve fibrosis or achievement of NASH resolution versus placebo. No new safety concerns were raised.

Dr. Lin (AI Evidence Lead): Statistical Endpoints & Numbers

Primary Endpoint & Quantitative Summary (The lancet. Gastroenterology & hepatology, 2023-06-15; N = 71; Rigor 88/100): In patients with NASH and compensated cirrhosis, semaglutide did not significantly improve fibrosis or achievement of NASH resolution versus placebo. No new safety concerns were raised.

Study Limitations & Caveats Before You Act

Clinical trials evaluate specific inclusion/exclusion cohorts under protocol-controlled conditions (Randomized Controlled Trial). Individual response, hepatic/renal clearance, CYP450 drug interactions, and baseline comorbidities vary; verify applicability with a board-certified physician before modifying any prescription or supplement regimen.

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