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Methods: A phase 3, multicenter, randomized (1:1), controlled, parallel-group, open-label study compares standard medical treatment (SMT) + Albutein 20% (1.5 g/Kg body weight, maximum 100 g/patient, every 10 2 days up to 12 mo

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Of the 150 patients identified through the Stanford Research Repository (STARR) tool, 18 met our inclusion criteria

Methods: This is a single center, prospective cohort study, which included all patients with decompensated ACLD (dACLD) due to HCV, older than 18 years, that had received DAA and achieved SVR, at our institution in Mexicali, Mexico, from January 1, 2018, to October 31, 2021