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Apixaban to Prevent Decompensation of Early Liver Cirrhosis Trial (APEACH)

21. juli 2026 opdateret af: University College, London

Apixaban to Prevent dEcompensation of eArly Liver CirrHosis Trial

Liver disease is the only common cause of death that is increasing in numbers. Once people develop severe scarring (cirrhosis), there are no medications proven to help them live longer, healthier lives. Apixaban is already commonly used to prevent or treat blood clots and is known to be safe for those with cirrhosis.

In the early stages of cirrhosis, most people have no symptoms and lead normal lives; this is called "compensated" cirrhosis. However, when the liver stops working properly, they develop "decompensated" cirrhosis, which causes yellow skin, confusion, vomiting of blood and painful fluid build-up. This is serious, and people are extremely unwell with a poor quality of life, often need to go to the hospital and on average only live for 2 more years.

The APEACH trial will investigate whether giving compensated cirrhosis patients Apixaban will help stop them from developing decompensated cirrhosis and stay in good health for longer.

Previous research studies suggest that taking blood-thinning drugs is safe and helpful for cirrhosis. However, these did not have enough participants to be confident enough in the results to recommend use in everyday clinical care.

The APEACH trial will include enough participants to make it clear whether Apixaban is helpful or not.

Studieoversigt

Status

Ikke rekrutterer endnu

Betingelser

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

1142

Fase

  • Fase 3

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Undersøgelse Kontakt Backup

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

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Ingen

Beskrivelse

Inclusion Criteria:

  1. Liver cirrhosis secondary to alcohol, with or without associated metabolic risk factors, i.e. Alcohol related liver disease (ARLD) or metabolic dysfunction-associated steatotic liver disease, where there has been a significant history of alcohol consumption (MetALD)
  2. Cirrhosis will be based on histology, or clear radiological evidence, e.g. nodular or heterogeneous liver or non-invasive testing (e.g. Fibroscan®, or Enhanced Liver Fibrosis (ELF) test
  3. Childs A Cirrhosis (Participants with a previous episode of decompensated cirrhosis who have now recompensated can be included)
  4. Participants with no hepatic encephalopathy or low-grade hepatic encephalopathy (Grade 0 or 1) taking lactulose and/or rifaximin
  5. Aged ≥18 years
  6. Clinical evidence of portal hypertension, defined as any 1 of:

    • Evidence of abdominal collateral circulation, recanalised umbilical vein or varices on imaging
    • Asymptomatic ascites (trace only) seen around the liver on imaging in patients who are not taking diuretics
    • Liver stiffness measurement >20kPa on FibroScan®/ Vibration- Controlled Transient Elastography (VCTE) (where BMI <35)
    • Presence of Gastro-oesophageal varices at endoscopy
    • Hepatic venous pressure gradient ≥ 10mmHg

Or Platelet count < 150,000 μL AND any 1 of:

  • Spleen size >13 cm in length
  • Liver stiffness measurement >20kPa on FibroScan®/VCTE (where BMI >35)
  • Presence of portal hypertensive gastropathy at endoscopy

Exclusion Criteria:

  1. Evidence of decompensation (e.g. ascites requiring treatment other than a thin rim around liver on imaging, as above) (Evidence of decompensation as follows: Grade 2 or 3 Ascites, Grade 2 - 4 Hepatic Encephalopathy, Variceal Haemorrhage)
  2. Causes for cirrhosis other than alcohol, including those with MASLD who have never drunk alcohol above government recommended levels (14 units/week)
  3. Pre-existing splanchnic vein thrombosis (portal, splenic, mesenteric, and hepatic veins)
  4. Use of (and need for) anticoagulation or dual antiplatelet therapy or clopidogrel
  5. Platelets <50x109/L at screening
  6. Moderate-severe renal impairment defined as eGFR <30ml/min at screening
  7. Recent variceal bleed or untreated large varices
  8. Malignancy in last 2 years if unlikely to survive trial because of comorbidity in the location PI's opinion
  9. Hepatocellular carcinoma
  10. Severe cardiac failure1 or Chronic Obstructive Pulmonary Disease (COPD)
  11. Pregnancy
  12. INR >1.7 (After vitamin K correction) at screening
  13. Previous hypersensitivity reaction to Apixaban

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Forebyggelse
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Firedobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Placebo komparator: Participants randomised to receive Apixaban 2.5mg oral tablet twice daily
Participants randomised to receive a matching placebo
Placebo will be given as oral tablet and taken twice daily
Eksperimentel: Participants randomised to receive Apixaban 2.5mg twice daily
Participants randomised to this arm will receive Apixaban 2.5mg twice daily

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Time from randomisation to first decompensation event, assessed up to 49 months
Tidsramme: Time from randomisation to first decompensation event, assessed up to 49 months

First decompensation event is defined as at least one of the following:

Grade 2 or 3 ascites according to the International Club of Ascites (ICA), or spontaneous bacterial peritonitis; Grade 2-4 hepatic encephalopathy; variceal haemorrhage (gastrointestinal bleeding secondary to rupture of varices); and liver-related death measured using METHOD at 6-monthly trial follow-up visits and throughout the trial, when location study teams become aware of these events, as decompensation normally involves hospitalisation

Time from randomisation to first decompensation event, assessed up to 49 months

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Time from randomisation to first decompensation event, assessed up to 49 months
Tidsramme: Time from randomisation to first decompensation event, assessed up to 49 months
Time to event for individual decompensation events measured at 6-monthly follow-up visits, assessed up to 49 months
Time from randomisation to first decompensation event, assessed up to 49 months
Time to development of grade 1 (small volume) ascites
Tidsramme: Time from randomisation assessed up to 49 months
Small volume ascites
Time from randomisation assessed up to 49 months
Assessment of safety of anticoagulation in Childs A cirrhosis patients
Tidsramme: Time from randomisation assessed up to 49 months
Assessment of safety of anticoagulation in Childs A cirrhosis patients, including incidence of clinically relevant combined major bleeding and non-major bleeding during trial treatment period
Time from randomisation assessed up to 49 months
Time to all-cause mortality
Tidsramme: Time from randomisation assessed up to 49 months
Time from randomisation assessed up to 49 months
Time to portal vein thrombosis or other thromboembolic events
Tidsramme: Time from randomisation assessed up to 49 months
Time from randomisation assessed up to 49 months
Incidence of cardiac events
Tidsramme: Time from randomisation assessed up to 49 months
Time from randomisation assessed up to 49 months
Alcohol use
Tidsramme: Time from baseline assessed up to 49 months
Alcohol use will be determined by patient reporting on AUDIT-C questionnaire
Time from baseline assessed up to 49 months
Health-related quality of life assessed using EQ-5D-5L questionnaire
Tidsramme: Time from randomisation assessed up to 49 months
Time from randomisation assessed up to 49 months

Andre resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Changes in FibroScan® liver stiffness measurement values, splenic elastography, and ELF values as an exploratory outcome
Tidsramme: Time from baseline assessed up to 49 months
This will be performed in scan performed and technology available
Time from baseline assessed up to 49 months
Progression or requirement for TIPSS or transplant as an exploratory outcome
Tidsramme: Time from randomisation assessed up to 49 months
Time from randomisation assessed up to 49 months
Time to diagnosis of hepatocellular carcinoma
Tidsramme: Time from randomisation assessed up to 49 months
Time from randomisation assessed up to 49 months
Disease progression, comparing changes in MELD and scores between beginning and end of trial
Tidsramme: Time from randomisation assessed up to 49 months
Time from randomisation assessed up to 49 months

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

15. juli 2026

Primær færdiggørelse (Anslået)

31. oktober 2030

Studieafslutning (Anslået)

30. marts 2031

Datoer for studieregistrering

Først indsendt

7. juli 2026

Først indsendt, der opfyldte QC-kriterier

21. juli 2026

Først opslået (Faktiske)

24. juli 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

24. juli 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

21. juli 2026

Sidst verificeret

1. juli 2026

Mere information

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