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Evaluation of Safety, efficacy, and QOL with Glecaprevir and Pibrentasvir therapy in Dialysis Patients Infected with Hepatitis C Virus

Evaluation of Safety, efficacy, and QOL with Glecaprevir and Pibrentasvir therapy in Dialysis Patients Infected with Hepatitis C Virus - Evaluation of Safety, efficacy, and QOL with Glecaprevir and Pibrentasvir therapy in Dialysis Patients Infected with Hepatitis C Virus

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000030229
Enrollment
10
Registered
2017-12-04
Start date
2017-12-08
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

Chronic hepatitis-C, Chronic Renal failure

Interventions

None listed

Sponsors

Kasama Chuo Clinic
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Depends on insurance adaptation

Exclusion criteria

Exclusion criteria: Depends on insurance adaptation

Design outcomes

Primary

MeasureTime frame
Sustained Virological Response at 12weeks after treatment

Secondary

MeasureTime frame
Safety and QOL during 6 months after treatment, and the period of treatment

Countries

Japan

Contacts

Public ContactMikio Sato

Kasama Chuo Clinic Internal medicine

hmsato@mail1.accsnet.ne.jp0296-71-6001

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026