Clinical Trials Directory

Trials / Completed

CompletedNCT02209740

Renal and Bone Outcome After Switching Tenofovir to Different Antiretroviral Strategies

A Prospective, Cohort Study of Renal and Bone Outcome After Changing Tenofovir in Patients With Renal Toxicity According to Antiretroviral Strategy

Status
Completed
Phase
Study type
Observational
Enrollment
245 (actual)
Sponsor
Asociacion para el Estudio de las Enfermedades Infecciosas · Network
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Renal outcome could be different after switching tenofovir to different antiretroviral strategies, in case of renal toxicity. Therefore, it is necessary to evaluate the importance of renal evolution in these patients, in terms of grade and time to renal improvement, according to the different options after interrupting tenofovir. The aim of this study was to explore the renal outcome after tenofovir according to new antiretroviral regimen.

Detailed description

Renal toxicity has become an important issue in a large number of HIV infected patients receiving a tenofovir-containing regimen. However, there are no data about the best antiretroviral regimen in patients switching tenofovir because of renal toxicity, in time, grade or persistence of renal improvement. Thus, patients with renal toxicity on tenofovir, defined as: * a progressive decrease of at least 25% of estimated glomerular filtration rate (GFR, by chronic kidney disease-epi equation), or * confirmed value of GFR below 60 ml/min in two successive determinations, or * proximal tubular renal dysfunction, as indicated by the presence of at least 3 of the following parameters: proteinuria\> 150 mg/g; excretion fractional of phosphorus in urine \> 20%; glucosuria \> 150 mg; or/and tubular proteinuria/albuminuria ratio above 0.4. who changed to the combination of abacavir plus a third drug, or to a nucleoside analogues-free antiretroviral combination (dual therapy, monotherapy) will be followed for 1 year to establish the time and grade of improvement (defined as the lack of above criteria).

Conditions

Interventions

TypeNameDescription
OTHERTenofovir switchPatients switched tenofovir to different antiretroviral regimen according to physicians decision

Timeline

Start date
2014-07-01
Primary completion
2015-12-01
Completion
2015-12-01
First posted
2014-08-06
Last updated
2015-12-30

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT02209740. Inclusion in this directory is not an endorsement.