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The purpose of this study is to evaluate the effects of sustained virological response in liver and spleen stiffness in patients with HCV compensated advanced chronic liver disease treated with new all oral antiviral drugs in order to determine factors implicated in stiffness change and its implications for long-term follow-up.
Full description
Prospective cohort study including consecutive patients (with baseline liver stiffness measurement ≥10 kPa who meet the Baveno VI criteria for compensated advanced chronic liver disease) who initiate treatment with new all oral antiviral drugs following current recommendations in Spain.
In all these patients the following parameters will be assessed:
Enrollment
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Inclusion criteria
Age 18 to 90 years.
History of chronic hepatitis C infection.
Compensated advanced chronic liver disease (Baveno VI definition):
Indication to start antiviral treatment with new oral drugs.
Willingness to enter the study.
Sign the informed consent.
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
41 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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