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Cost-effectiveness of Different Antiretroviral Treatment in Patients HIV Naive

Patient Compliance Clinical Trial

Official title:
Cost-effectiveness of Different Antiretroviral Treatment in Patients HIV Naive. Randomized Clinical, Not Masked, Trial Comparing DRVr3TC, ABC3TC (Kivexa) RPV, or EVG COBI FTC TDF (Stribild) for 48 Weeks

Clinical Trial Summary

The main objective of this study is to know the efficiency (costeffectiveness) at 48 weeks of initiation of antiretroviral treatment. three strategies of treatment.

Clinical Trial Description

Secondary objectives:

- patients with virologic response ratio at 48 weeks (less than 50 plasma viral load)

- Change in the number of CD4 cells at 48 weeks

- Change in body composition and mineral density bone (body and lumbar) measurement with DEXA (bone mineral density scan) at 48 weeks

- Change in markers of renal function (creatinine clearance, glomerular filtration rate - eGFR - estimated rate) and renal tubular function at 48 weeks

- Rate of mortality and clinical progression at 48 weeks

- general tolerability and safety: adverse events (AA) and serious AA description ;

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02470650
Study type Interventional
Source Hospital Clinic of Barcelona
Contact Pep Mallolas, MD
Email jmallolas@clinic.ub.es
Status Recruiting
Phase Phase 4
Start date June 2015
Completion date October 2017
View Details
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