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Clinical Trial Summary

Retrospective cohort of virologically suppressed HIV-infected patients who received the combination of Raltegravir plus Darunavir boosted with cobicistat or ritonavir, as dual therapy, because or toxicity or intolerance to nucleoside analogues


Clinical Trial Description

This is a retrospective cohort study including those HIV-infected patients who received the combination of raltegravir plus darunavir boosted with cobicistat or ritonavir as dual therapy, due to the existence of toxicity or intolerance to nucleoside analogues, to evaluate:

- efficacy, measured as percentage of patients free of virological failure after 48 and 96 weeks (ITT-e, snapchot analysis) and improvement in CD4+ count

- tolerance (rate of discontinuation and cause, and frequency of adverse events)

- evolution of different comorbidities (renal, bone, cardiovascular events)

Patients will included if they have received at least 1 dose of the dual therapy ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03348449
Study type Observational
Source Asociacion para el Estudio de las Enfermedades Infecciosas
Contact
Status Completed
Phase
Start date December 15, 2017
Completion date June 29, 2018

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