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Prognostic Model of HCV-related Disease Progression After DAAs

Prognostic Model of HCV-related Disease Progression After DAAs

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04631640
Enrollment
234
Registered
2020-11-17
Start date
2020-12-01
Completion date
2024-12-31
Last updated
2020-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HCV

Keywords

HCV

Brief summary

In this study, the investigator would conduct an ambispective cohort study to build a prediction model of HCV-related disease after DAAs.

Detailed description

The emergence of direct antiviral agents (DAAs) makes it possible to cure HCV, and the sustained virological response (SVR) rate is up to 90% after DAAs therapy. However, the acquisition of SVR does not mean the cure of HCV-related diseases, some patients still developed liver cirrhosis, liver cancer and other diseases after achived SVR by DAAs therapy.In this study the investigator would like to bulid a prediction model of HCV-related disease after DAAs by conducting an ambispective cohort study. The participants of this study would be adult patients (≥18 years old) with chronic HCV infection and have received DAA therapy, the investigator would retrospectively collected DAA therapy-related information, and follow-up all the enrolled participants every 6 months to observe their liver-related disease outcomes (composite liver outcome, including liver-related deaths, hepatocellular carcinoma, liver decompensation, and liver transplantation).

Interventions

None listed

Sponsors

Peking University People's Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* adult patients (≥18 years old) with chronic HCV infection that were HCV RNA positive; * have received DAA treatment; * would like to adhere to the follow-up

Exclusion criteria

* lack of HCV treatment information;

Design outcomes

Primary

MeasureTime frameDescription
incidence of composit liver-related eventsthrough study completion, an average of 2 yearComposite liver outcomes, including liver-related deaths, hepatocellular carcinoma, liver decompensation, or liver transplantation.

Contacts

Primary ContactHuixin Liu, Ph.D.
lhxepi@163.com15810994780

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026