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Adherence to Dolutegravir and Outcome — DOLUTECAPS  

HIV Clinical Trial

Official title:
Cohort Study to Assess Electronic-caps Defined Adherence Patterns - Virological Outcome Relationship Amongst HIV-1 Infected Subjects Receiving Dolutegravir-Based Antiretroviral Therapy)

Clinical Trial Summary

The main assumption is that the dolutegravir can get virologic suppression to suboptimal adherence levels (between 80 and 95%, and after treatment interruptions) where other molecules are not capable, due to their pharmacokinetic/pharmacodynamic (pardonnance).

While the investigators goal is not to compare molecules (study with one arm) in terms of forgiveness, the results of this cohort in terms of forgiveness could be compared to other cohorts available.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02878642
Study type Observational
Source University Hospital, Caen
Contact Jean Jacques PARIENTI, MD,PhD
Phone 02 31 06 43 20
Email parienti-jj@chu-caen.fr
Status Recruiting
Phase N/A
Start date May 2015
Completion date December 2017
View Details
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