Clinical Trials Directory

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UnknownNCT02878642

Adherence to Dolutegravir and Outcome

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

Status
Unknown
Phase
Study type
Observational
Enrollment
120 (estimated)
Sponsor
University Hospital, Caen · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Timeline

Start date
2015-05-01
Primary completion
2017-12-01
Completion
2017-12-01
First posted
2016-08-25
Last updated
2017-02-01

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT02878642. Inclusion in this directory is not an endorsement.