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Outcome of early switching of Tenofovir Disoproxil Fumarate (TDF) in HIV-infected patients with TDF-induced nephrotoxicity: a prospective study

Outcome of early switching of Tenofovir Disoproxil Fumarate (TDF) in HIV-infected patients with TDF-induced nephrotoxicity: a prospective study

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20190307003
Enrollment
64
Registered
2019-03-07
Start date
2017-09-30
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

TDF&#45

Interventions

switching of TDF to alternative ART,Late&#45
switching of TDF to alternative ART
Experimental Other,Experimental Other
switching of TDF,Late&#45
switching of TDF

Sponsors

None listed

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: HIV-infected adult age of 18 years old or more plus the followings: 1) on TDF-containing regimen 2) no documented HIV drug resistance 3) evidence of proximal renal tubulopathy (PRT) 4) protease inhibitor-naïve patients

Exclusion criteria

Exclusion criteria: 1) any concomitant kidney disease or abnormal urinary sediments before TDF initiation 2) nephrotoxic agents or MRP-4 inhibitors use in the previous 28 days prior to recruitment 3) pregnant patients 4) documented obstructive uropathy including BPH and stones 5) SGLT-2 inhibitors use.

Design outcomes

Primary

MeasureTime frame
Complete recovery of proximal tubular markers 1 year Tubular markers

Secondary

MeasureTime frame
Virological outcome 1 year HIV viral load

Contacts

Public ContactSamadhi Patamatamkul

Chulalongkorn University

samadhi.p@msu.ac.th66815441374

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026