Direct Acting Antivirals for HCV Infection in Kidney Transplant Recipients

Istanbul University

Status: Completed

Conditions: Hepatitis C, Chronic; Kidney Transplant; Complications

Study type: Observational

Funder types: Other

Identifiers

NCT03880682

2018/1511

Details and patient eligibility

About

Chronic hepatitis C virus (HCV) infection, an important cause of morbidity and mortality worldwide, is a significant problem in kidney transplant recipients (KTRs) given its high prevalence in patients undergoing hemodialysis. Interferon based regimens were cornerstone of treatment of HCV infection in the past; however, due to their low efficacy and high rates of adverse effects, they have been abandoned in the new era of direct acting antivirals (DAAs). Several studies demonstrated the efficacy and safety of DAAs, yet data regarding clinical practice of these agents in KTRs is still needed. Therefore, we conducted a study using our registry data to evaluate the efficacy and safety of DAAs in KTRs.

Enrollment: 30 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Being a kidney transplant recipient.
• Having a detectable level of HCV RNA.
• Having direct acting antivirals for 12 or 24 weeks.

Exclusion criteria

• Withdrawing or not providing consent.

Trial design

30 participants in 1 patient group

Study Group

Description:

Kidney transplant recipients with chronic HCV infection who were treated using direct acting antivirals.