Literature DB >> 32896580

Endpoints and design of clinical trials in patients with decompensated cirrhosis: Position paper of the LiverHope Consortium.

Elsa Solà1, Elisa Pose1, Daniela Campion2, Salvatore Piano3, Olivier Roux4, Macarena Simon-Talero5, Frank Uschner6, Koos de Wit7, Giacomo Zaccherini8, Carlo Alessandria2, Ulrich Beuers7, Paolo Caraceni8, Claire Francoz4, Rajeshwar P Mookerjee9, Jonel Trebicka6, Victor Vargas5, Miquel Serra10, Ferran Torres11, Sara Montagnese12, Aleksander Krag13, Ruben Hernaez14, Marko Korenjak15, Hugh Watson16, Juan G Abraldes17, Patrick S Kamath18, Pere Ginès19.   

Abstract

Management of decompensated cirrhosis is currently geared towards the treatment of complications once they occur. To date there is no established disease-modifying therapy aimed at halting progression of the disease and preventing the development of complications in patients with decompensated cirrhosis. The design of clinical trials to investigate new therapies for patients with decompensated cirrhosis is complex. The population of patients with decompensated cirrhosis is heterogeneous (i.e., different etiologies, comorbidities and disease severity), leading to the inclusion of diverse populations in clinical trials. In addition, primary endpoints selected for trials that include patients with decompensated cirrhosis are not homogeneous and at times may not be appropriate. This leads to difficulties in comparing results obtained from different trials. Against this background, the LiverHope Consortium organized a meeting of experts, the goal of which was to develop recommendations for the design of clinical trials and to define appropriate endpoints, both for trials aimed at modifying the natural history and preventing progression of decompensated cirrhosis, as well as for trials aimed at managing the individual complications of cirrhosis.
Copyright © 2020 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  ACLF; AKI; Ascites; Cirrhosis; Clinical trials; Endpoints; Hepatic encephalopathy; Hyponatremia; Infections; Liver transplant; Quality of life

Mesh:

Year:  2020        PMID: 32896580     DOI: 10.1016/j.jhep.2020.08.009

Source DB:  PubMed          Journal:  J Hepatol        ISSN: 0168-8278            Impact factor:   25.083


  2 in total

1.  Leveraging electronic health record data for clinical trial planning by assessing eligibility criteria's impact on patient count and safety.

Authors:  James R Rogers; Jovana Pavisic; Casey N Ta; Cong Liu; Ali Soroush; Ying Kuen Cheung; George Hripcsak; Chunhua Weng
Journal:  J Biomed Inform       Date:  2022-02-18       Impact factor: 6.317

2.  Patterns of acute decompensation in hospitalized patients with cirrhosis and course of acute-on-chronic liver failure.

Authors:  Lorenz Balcar; Georg Semmler; Katharina Pomej; Benedikt Simbrunner; David Bauer; Lukas Hartl; Mathias Jachs; Rafael Paternostro; Theresa Bucsics; Matthias Pinter; Michael Trauner; Mattias Mandorfer; Thomas Reiberger; Bernhard Scheiner
Journal:  United European Gastroenterol J       Date:  2021-05       Impact factor: 4.623

  2 in total

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