Evaluation of the efficacy of glecaprevir and pibrentasvir for Japanese hepatitis C patients: a prospective study in real life settings.

Evaluation of the efficacy of glecaprevir and pibrentasvir for Japanese hepatitis C patients: a prospective study in real life settings. - The efficacy of glecaprevir and pibrentasvir for Japanese hepatitis C patients.

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000031664

Enrollment

350

Registered

2018-03-12

Start date

2017-12-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

cirrhotic and non cirrhotic patients with chronic hepatitis C virus

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: chronic hepatitis C and compensated cirrhotic patients with HCV RNA

Exclusion criteria

Exclusion criteria: decompensated cirrhosis

Design outcomes

Primary

Measure	Time frame
sustained virological response (SVR) at 12 week and 24 week after the end of treatment	—

Secondary

Measure	Time frame
incidence rate of adverse events sustained virological response (SVR) at 4 week after the end of treatment	—

Countries

Japan

Contacts

Public ContactHitomi Sezaki

Toranomon Hospital hepatology

hitomis@mx1.harmonix.ne.jp03-3588-1111

Outcome results