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临床试验/NCT05452187
NCT05452187已完成不适用

Evaluation of the Safety and Effectiveness of Direct-acting Antiviral Drugs in the Treatment of Hepatitis C in Patients With Inflammatory Bowel Disease: National Multicenter Study (MIC Project).

Hospital Mutua de Terrassa1 个研究点 分布在 1 个国家目标入组 79 人开始时间: 2021年3月12日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
79
试验地点
1
主要终点
Percentage of sustained viral response (effectiveness) in patients with IBD and HCV infection treated with DAAs.

研究概览

简要总结

The prevalence of hepatitis C virus infection (HCV) in patients with inflammatory bowel disease (IBD) ranges from 1-6%. Direct-acting antivirals (DAAs), with cure rates >90%, represent a radical change from interferon-based therapies. The ECCO (European Crohn's and Colitis Organisation) guidelines (Kucharzik T, Ellul P, Greuter T, et al. ECCO Guidelines on the Prevention, Diagnosis, and Management of Infections in Inflammatory Bowel Disease. J Crohn's Colitis. 2021;15(6):879-913) warns about the risk of IBD reactivation due to the effect of DAAs, but HCV management in this situation is uncertain given the lack of evidence.

The project is proposed as the largest retrospective multicenter descriptive study carried out to evaluate the use of DAAs for HCV eradication in patients with IBD. The Eneida database (Zabana Y, Panés J, Nos P, et al. The ENEIDA registry (Nationwide study on genetic and environmental determinants of inflammatory bowel disease) by GETECCU: Design, monitoring, and functions. Gastroenterol y Hepatol. 2020;43(9):551-8.) of the Spanish Working Group on Crohn's Disease and Ulcerative Colitis (GETECCU) is an adequate registry to identify patients with HCV infection. The serological status of the infection is frequently recorded in the ENEIDA database, and it is generally evaluated at the time of IBD diagnosis, before starting immunosuppressive treatment. The ENEIDA registry has the advantage over large population studies that researchers have access to relevant details of the clinical history, which can respond to the controversies raised.

This multicenter retrospective descriptive study will provide useful information to be able to give evidence-based recommendations regarding treatment of HCV in patients with IBD.

详细描述

Hypothesis

The use of DAAs for HCV eradication in patients with IBD is effective and safe. DAAs do not trigger IBD flares. DAAs probably do not present serious pharmacological interactions, with clinically relevant, with immunosuppressants and/or biological agents.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者

入选标准

  • All individuals diagnosed with IBD according to the ECCO criteria and chronic HCV infection (positive HCV Ab and detectable RNA) treated with DAAs and/or interferon collected in the ENEIDA database, and who have properly completed the fields of age, gender, treatment, location, and phenotype of IBD, will be included in the study.
  • Study period: Patients treated with DAAs between January 1, 2011 - February 28, 2021.

排除标准

  • Spontaneous cure of HCV without treatment
  • HCV treatment outside the study period.

研究组 & 干预措施

Patients with IBD and chronic HCV infection treated with DAAs and/or interferon.

Cohort patients with IBD and chronic HCV infection treated with DAAs and/or interferon collected from the ENEIDA database.

干预措施: Assess the effectiveness and safety of DAAs in patients with IBD. (Drug)

Patients with IBD and chronic HCV infection treated with DAAs and/or interferon.

Cohort patients with IBD and chronic HCV infection treated with DAAs and/or interferon collected from the ENEIDA database.

干预措施: Evaluate the interaction of DAAs with IBD drugs, particularly immunosuppressants and/or biologics. (Drug)

Patients with IBD and chronic HCV infection treated with DAAs and/or interferon.

Cohort patients with IBD and chronic HCV infection treated with DAAs and/or interferon collected from the ENEIDA database.

干预措施: Assessment of the impact of DAAs on the course of IBD. (Other)

结局指标

主要结局

Percentage of sustained viral response (effectiveness) in patients with IBD and HCV infection treated with DAAs.

时间窗: 8 weeks

Number and description of adverse events (safety) and possible interactions of DAAs with IBD drugs, particularly immunosuppressants and/or biologics.

时间窗: 8 weeks

次要结局

  • Compare the clinical Crohn's disease activity (measured by Harvey Bradshaw Index) before and during the treatment with DAAs, to assess the impact of DAAs on the course of IBD.(8 weeks)
  • Compare the clinical ulcerative colitis activity (measured by Partial Mayo Score) before and during the treatment with DAAs, to assess the impact of DAAs on the course of IBD.(8 weeks)

研究者

发起方
Hospital Mutua de Terrassa
申办方类型
Other
责任方
Sponsor

研究点 (1)

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