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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)

H

Hospital Mutua de Terrassa

Status

Completed

Conditions

Inflammatory Bowel Diseases
Hepatitis C Virus Infection

Treatments

Other: Assessment of the impact of DAAs on the course of IBD.
Drug: Evaluate the interaction of DAAs with IBD drugs, particularly immunosuppressants and/or biologics.
Drug: Assess the effectiveness and safety of DAAs in patients with IBD.

Study type

Observational

Funder types

Other

Identifiers

NCT05452187
MIC2020

Details and patient eligibility

About

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.

Full description

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.

Enrollment

79 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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.

Exclusion criteria

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

Trial design

79 participants in 1 patient group

Patients with IBD and chronic HCV infection treated with DAAs and/or interferon.
Description:
Cohort patients with IBD and chronic HCV infection treated with DAAs and/or interferon collected from the ENEIDA database.
Treatment:
Drug: Assess the effectiveness and safety of DAAs in patients with IBD.
Drug: Evaluate the interaction of DAAs with IBD drugs, particularly immunosuppressants and/or biologics.
Other: Assessment of the impact of DAAs on the course of IBD.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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