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OpenTrials
Completed

NCT Number: NCT03346941

Side Effects After Direct-acting Antiviral Treatment

The objective of this study was to assess the incidence of side effects after direct-acting antiviral therapy in patients with chronic hepatitis C virus infection.

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Key information

About this study

Direct-acting antiviral (DAA)-based treatments are today very effective The objective of this study was to assess the incidence of side effects after DAA therapy in patients with chronic hepatitis C virus infection.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 years of age or older
  • Hepatitis C virus infection
  • Treatment by direct-acting antiviral combination

Exclusion criteria

  • HIV coinfection

Treatment and study plan

DAA treatment

Drug

Direct-acting antiviral-based treatment

Primary outcomes

  1. Incidence of side effects

    Time frame: Within treatment duration, i.e. 8, 12 or 24 weeks after treatment initiation

    Incidence of side effects occurring during treatment duration. Treatment duration may be of 8 weeks, 12 weeks or 24 weeks depending on treatment combination.

Sponsors and collaborators

Lead sponsor

Hospices Civils de Lyon

Other

Registry information

Official study title

Side Effects After Direct-acting Antiviral Treatment in Patients With Chronic Hepatitis C. The EFINO-C Study.

Acronym: EFINO-C

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Nov 20, 2017
Registry last updated
Nov 20, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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