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

2026년 7월 21일 업데이트: 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.

연구 개요

상태

아직 모집하지 않음

정황

연구 유형

중재적

등록 (추정된)

1142

단계

  • 3단계

연락처 및 위치

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연구 연락처

연구 연락처 백업

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

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

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 방지
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 네 배로

무기와 개입

참가자 그룹 / 팔
개입 / 치료
위약 비교기: 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
실험적: Participants randomised to receive Apixaban 2.5mg twice daily
Participants randomised to this arm will receive Apixaban 2.5mg twice daily

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Time from randomisation to first decompensation event, assessed up to 49 months
기간: 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

2차 결과 측정

결과 측정
측정값 설명
기간
Time from randomisation to first decompensation event, assessed up to 49 months
기간: 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
기간: 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
기간: 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
기간: 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
기간: Time from randomisation assessed up to 49 months
Time from randomisation assessed up to 49 months
Incidence of cardiac events
기간: Time from randomisation assessed up to 49 months
Time from randomisation assessed up to 49 months
Alcohol use
기간: 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
기간: Time from randomisation assessed up to 49 months
Time from randomisation assessed up to 49 months

기타 결과 측정

결과 측정
측정값 설명
기간
Changes in FibroScan® liver stiffness measurement values, splenic elastography, and ELF values as an exploratory outcome
기간: 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
기간: Time from randomisation assessed up to 49 months
Time from randomisation assessed up to 49 months
Time to diagnosis of hepatocellular carcinoma
기간: 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
기간: Time from randomisation assessed up to 49 months
Time from randomisation assessed up to 49 months

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 7월 15일

기본 완료 (추정된)

2030년 10월 31일

연구 완료 (추정된)

2031년 3월 30일

연구 등록 날짜

최초 제출

2026년 7월 7일

QC 기준을 충족하는 최초 제출

2026년 7월 21일

처음 게시됨 (실제)

2026년 7월 24일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 7월 24일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 7월 21일

마지막으로 확인됨

2026년 7월 1일

추가 정보

이 연구와 관련된 용어

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

미정

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

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미국 FDA 규제 기기 제품 연구

아니

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간경화에 대한 임상 시험

Placebo에 대한 임상 시험

구독하다