HIV infection
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) HIV-infected patients who visited Kyushu-university hospital from January 1, 2013 to December 31, 2018. (2)Patients after switching TDF to TAF containing ART regimens in which virologically suppressed (HIV RNA< 20 copies/mL) for at least 6 months (3)Patients remain on the same third agent after switching to TAF/FTC containing regimen (4)Patients received an explanation of the study protocol and gave written informed consent. (5)Patients whose age is over 20 on informed consent acquisition date
Exclusion criteria
Exclusion criteria: Patients are inadequate to include in this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Efficacy for maintenance of virological suppression in HIV-infected patients 48 weeks after switching from tenofovir disoproxil fumarate to tenofovir alafenamide containing antiretroviral therapy. | — |
Secondary
| Measure | Time frame |
|---|---|
| Efficacy for improvement of renal function and bone metabolism markers, rate of new HBV infection 48 weeks after switching from tenofovir disoproxil fumarate to tenofovir alafenamide containing antiretroviral therapy. | — |
Countries
Japan
Contacts
Kyushu University Hospital Department of General internal medicine