<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Patel VC</submitter><funding>National Institute for Health Research (NIHR)</funding><pagination>265</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11022376</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>25(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Liver disease is within the top five causes of premature death in adults. Deaths caused by complications of cirrhosis continue to rise, whilst deaths related to other non-liver disease areas are declining. Portal hypertension is the primary sequelae of cirrhosis and is associated with the development of variceal haemorrhage, ascites, hepatic encephalopathy and infection, collectively termed hepatic decompensation, which leads to hospitalisation and mortality. It remains uncertain whether administering a non-selective beta-blocker (NSBB), specifically carvedilol, at an earlier stage, i.e. when oesophageal varices are small, can prevent VH and reduce all-cause decompensation (ACD).&lt;h4>Methods/design&lt;/h4>The BOPPP trial is a pragmatic, multicentre, placebo-controlled, tripl</pubmed_abstract><journal>Trials</journal><pubmed_title>Beta-blockers or Placebo for Primary Prophylaxis (BOPPP) of oesophageal varices: study protocol for a randomised controlled trial.</pubmed_title><pmcid>PMC11022376</pmcid><funding_grant_id>17/32/04</funding_grant_id><pubmed_authors>Naylor S</pubmed_authors><pubmed_authors>Hudson B</pubmed_authors><pubmed_authors>Eastgate C</pubmed_authors><pubmed_authors>Burge T</pubmed_authors><pubmed_authors>Phiri E</pubmed_authors><pubmed_authors>Biju A</pubmed_authors><pubmed_authors>Williams A</pubmed_authors><pubmed_authors>Austin A</pubmed_authors><pubmed_authors>Pelaez CJ</pubmed_authors><pubmed_authors>Finlay 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S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Beta-blockers or Placebo for Primary Prophylaxis (BOPPP) of oesophageal varices: study protocol for a randomised controlled trial.</name><description>&lt;h4>Background&lt;/h4>Liver disease is within the top five causes of premature death in adults. Deaths caused by complications of cirrhosis continue to rise, whilst deaths related to other non-liver disease areas are declining. Portal hypertension is the primary sequelae of cirrhosis and is associated with the development of variceal haemorrhage, ascites, hepatic encephalopathy and infection, collectively termed hepatic decompensation, which leads to hospitalisation and mortality. It remains uncertain whether administering a non-selective beta-blocker (NSBB), specifically carvedilol, at an earlier stage, i.e. when oesophageal varices are small, can prevent VH and reduce all-cause decompensation (ACD).&lt;h4>Methods/design&lt;/h4>The BOPPP trial is a pragmatic, multicentre, placebo-controlled, tripl</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2026-05-29T10:25:45.979Z</modification><creation>2026-04-08T04:26:47.946Z</creation></dates><accession>S-EPMC11022376</accession><cross_references><pubmed>38627804</pubmed><doi>10.1186/s13063-024-08063-3</doi></cross_references></HashMap>