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临床试验/NCT06223893
NCT06223893招募中不适用

CirrhoCare, A Real-world, Randomised Controlled Study, to Determine the Clinical and Cost-effectiveness of CirrhoCare Digital Home Monitoring and Management in Patients With Decompensated Cirrhosis

University College, London30 个研究点 分布在 1 个国家目标入组 214 人开始时间: 2023年11月24日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
214
试验地点
30
主要终点
Number of hospital interventions from new-liver related complications

研究概览

简要总结

The CirrhoCare trial is a multi-centre, open label randomised controlled trial in patients with decompensated cirrhosis. The trial aims to investigate the clinical and cost-effectiveness of CirrhoCare digital home monitoring and management with current standard of care in these patients.

详细描述

Cirrhosis, progressive scaring of the liver- has many causes, principally, excessive alcohol intake, fatty-liver and viral infections. Unlike many chronic diseases, cirrhosis deaths are increasing rapidly year-on-year. It is the third commonest cause of premature, UK working-age deaths, with 62,000 years of working-life lost each year and NHS care costs of £4.53bn annually. One quarter of all UK cirrhosis patients are at-risk of acute decompensation, whereby complications such as fluid-overload, confusion and infections arise, requiring hospital-emergency treatment.

Currently, decompensated cirrhosis patients require regular hospital clinical assessments to detect these new complications. Even following hospital discharge, readmission with new decompensating complications approaches 37% in 4 weeks. This disease burden, compounded by increasing alcohol and obesity-driven liver disease, means demand for specialist liver services outweighs current capacity in a resource-stretched healthcare system. Moreover, regional variation of specialist liver services also impacts on illness and deaths, leading to a postcode lottery of care access and geographical inequity.

The CirrhoCare trial, addresses this urgent clinical-need through an innovative cirrhosis management system, including home-monitoring of decompensated cirrhosis patients, measuring vital signs such as heart rate and blood pressure (using low cost, sensing technology), assessing weight (smart-scale) and mental ability (smartphone app), all of which are impacted as cirrhosis progresses. By efficiently and securely collecting data on CyberLiver's management-system (platform), CirrhoCare provides a decision-facilitating tool, incorporating individual-patient data, helping liver-physicians to optimise and personalise treatment in the community.

The CirrhoCare trial investigators also plan to assess clinical and cost effectiveness of CirrhoCare management and seek regulatory approvals. This innovative aspect of cirrhosis management will be more acceptable and convenient for patients. It will also deliver community care with environmental, sustainable benefits, through reduced hospital visits, despite increasing service demands. The cost- effectiveness analysis will generate value-for-money evidence of CirrhoCare management, and the clinical evidence needed to inform future adoption into the NHS.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Number of hospital interventions from new-liver related complications

时间窗: 90 days from randomisation

The CirrhoCare trial will investigate whether the CirrhoCare management system leads to a reduction in the requirement for unplanned medical intervention from new-liver related complications over 90 days from hospital discharge.

次要结局

  • Number of hospital readmissions(90 days from randomisation)
  • User experience and engagement(90 days from randomisation)
  • Healthcare resource use analysis(90 days from randomisation)
  • Healthcare cost analysis(90 days from randomisation)
  • Quality of Life (EQ-5D-5L) assessment(90 days from randomisation)
  • Frailty assessment(90 days from randomisation)
  • Mortality(90 days from randomisation)
  • Effects on CLIF-C AD score(90 days from randomisation)
  • Effects on MELD score(90 days from randomisation)
  • To determine the effects of the CirrhoCare management system on the number of liver-related deaths at 90 days(90 days from randomisation)
  • Effects of the individual components making up the primary outcome(90 days from randomisation)
  • Longitudinal effects of all secondary outcomes(Day 28, Day 56, Day 90)
  • Length of hospital readmissions(90 days from randomisation)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (30)

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