Outcome
Type |
Measure |
Description |
Time frame |
Safety issue |
Other |
Change in CD4 cell count from baseline to week 48 |
The CD4 cell counts will be obtained at baseline and week 48. |
Week 0 and 48 |
|
Other |
Change in metabolic variables (cholesterol) |
Change in total cholesterol |
Week 0 and 48 |
|
Other |
Change in metabolic variables (low density lipoprotein) |
Change in low density lipoprotein-cholesterol |
Week 0 and 48 |
|
Other |
Change in metabolic variables (high density lipoprotein) |
Change in high density lipoprotein-cholesterol |
Week 0 and 48 |
|
Other |
Change in metabolic variables (triglycerides) |
Change in triglycerides |
Week 0 and 48 |
|
Other |
Change in body weight |
Change in body weight from baseline to week 48 |
Week 0 and 48 |
|
Other |
Change in BMI |
Change in BMI from baseline to week 48 |
Week 0 and 48 |
|
Other |
Change in renal function, assessed by glomerular filtration rate |
Changes in glomerular filtration rate (calculated using the Chronic Kidney Disease Epidemiology Collaboration [CKD-EPI] formula) from baseline to week 48 |
Week 0 and 48 |
|
Other |
Change in renal function, assessed by urine protein-to-creatinine ratio |
Change in renal function (glomerular filtration rate) using the urine protein-to-creatinine ratio from baseline to week 48 |
Week 0 and 48 |
|
Other |
Proportion of patients with new drug-related CNS symptom(s) at week 4 |
Proportion of patients with new drug-related central nervous system (CNS) symptom(s) at the 4 week visit. |
Week 4 |
|
Other |
Proportion of patients with new drug-related CNS symptom(s) reporting new drug-related CNS symptom(s) at any time point between baseline and week 48. |
Occurrence of CNS Adverse Events (AEs) in patients new to DTG |
Week 0 to 48 |
|
Other |
Proportion of patients with a Serious Adverse Event (SAE) at any time point |
Proportion of patients with a SAE, graded using the Division of AIDS table for grading AEs at any time point. |
Week 0 to 48 |
|
Primary |
Loss of viral suppression |
Difference in the proportion of individuals with an HIV-RNA =50 cp/mL at 48 weeks between the treatment arms. |
Week 48 |
|
Secondary |
Changes in DDI score from week 0 to 48 |
Using the University of Liverpool Drug Database (https://www.hiv-druginteractions.org/), the prescribed ART and co-medications will be categorized as red flag (3 points) for severe DDIs when co-administration is contraindicated, amber flag (2 points) for potential clinically significant DDIs manageable by dose adjustment or clinical monitoring, yellow flag (1 point) for DDIs of weak clinical relevance with no need of a priori dosage adjustment or monitoring, and a green flag (0 points) for no interactions. Amber flag DDIs will be downgraded to 1 point if there is evidence that the DDI was managed correctly (i.e. DTG administered 2 hours before or 6 hours after taking divalent cations). The sum of all points at visit 6, week 48 will be compared to baseline. |
Week 0 and 48 |
|
Secondary |
Patient report outcomes concerning changes in treatment satisfaction between baseline and 48 weeks, as determined using the HIV Treatment Satisfaction Questionnaire HIVTSQc (change version). |
The investigators will assess changes in treatment satisfaction between week 0 and 48 using the validated HIV Treatment Satisfaction Questionnaire HIVTSQc (change version). |
Week 0 to 48 |
|
Secondary |
Proportion of patients experiencing confirmed virological failure |
Proportion of patients experiencing confirmed virological failure, defined as 2 consecutive plasma HIV viral loads =200 copies/mL |
Week 48 |
|
Secondary |
Proportion of individuals detected with new drug resistance |
Proportion of individuals experiencing impairment / loss of future drug options throughout the study period, defined as new detection of resistance-associated mutations against DOR, DTG, 3TC (intervention-arm) or against the components of the ART regimen that the virus was considered to be sensitive to at randomization (based on historic resistance testing or treatment history; control-arm). |
Week 0 to 48 |
|
Secondary |
Proportion of individuals with any moderate (orange flag) or severe (red flag) DDI |
Proportion of individuals with any moderate (orange flag) or severe (red flag) DDI at any study visit between baseline and week 48, based on the results from the Liverpool drug interaction database (www.hiv-druginteractions.org). |
Week 0 to 48 |
|
Secondary |
Proportion of patients with DDI leading to suboptimal management of comorbidities |
Proportion of patients with DDI leading to suboptimal management of comorbidities between baseline and week 48, as reported by the cohort physician. |
Week 0 and 48 |
|
Secondary |
Patient report outcomes concerning differences in quality of life between both groups at week 48 assessed by the World Health Organization Quality-of-Life- HIV Bref (WHOQOL-HIV BREF) questionnaire |
Differences in quality of life between both groups at week 48, assessed using the World Health Organization Quality-of-Life- HIV Bref (WHOQOL-HIV BREF) questionnaire |
Week 48 |
|
Secondary |
Patient report outcomes concerning differences in treatment satisfaction between both groups assessed by HIV Treatment Satisfaction Questionnaires |
The investigators will assess the differences in treatment satisfaction between both groups at week 48, as determined using the validated HIV Treatment Satisfaction Questionnaires HIVTSQ. |
Week 48 |
|
Secondary |
Proportion of individuals reporting depression assessed by Patient Health Questionnaire-9 |
Depression will be assessed at baseline and week 48, assessed using the Patient Health Questionnaire-9 (PHQ-9) |
Week 0 and 48 |
|
Secondary |
Changes in intact proviral HIV-DNA levels |
Changes in intact proviral HIV-DNA levels in peripheral blood mononuclear cells (PBMCs) between baseline and week 48. Stored PBMC samples will be used to determine HIV-DNA levels by a digital droplet PCR (ddPCR) assay using the RAINDANCE system. |
Week 0 to 48 |
|
Secondary |
Proportion of individuals who develop a detectable HBV viral load |
Proportion of individuals with a positive anti-HBc and negative anti-HBs ("anti-HBc alone") who develop a detectable HBV viral load (>50 IU/mL) at weeks 24 and 48. |
Weeks 24 and 48 |
|
Secondary |
Cumulative cost of all ART drugs used |
The 48-weeks cumulative cost of the received ART regimen will be calculated using prices published by the Federal Office of Public Health (https://www.spezialitaetenliste.ch/ShowPreparations.aspx). |
Week 0 to 48 |
|
Secondary |
Perception of the trial and/or of HIV-related research in general assessed by qualitative interviews in a subset of approximately 30 trial participants |
Perception of the trial and/or of HIV-related research in general. |
Week 0 and 48 |
|
Secondary |
Acceptability conditions of participation in the trial assessed by qualitative interviews in a subset of approximately 30 trial participants |
Acceptability conditions, understood as all barriers and facilitators to be involved in a trial. |
Week 0 and 48 |
|
Secondary |
Needs regarding the booster-free regimen or regarding ART in general assessed by qualitative interviews in a subset of approximately 30 trial participants |
Needs regarding the booster-free regimen or regarding ART in general for participants included in the observational cohort. |
Week 0 and 48 |
|
Secondary |
Expectations regarding the booster-free regimen or regarding ART in general assessed by qualitative interviews in a subset of approximately 30 trial participants |
Expectations regarding the booster-free regimen or regarding ART in general for participants included in the observational cohort. |
Week 0 and 48 |
|
Secondary |
Perspectives on how the participants' current and anticipated needs can be assessed by qualitative interviews in a subset of approximately 30 trial participants |
Perspectives on how the participants' current and anticipated needs can be addressed by research. |
Week 0 and 48 |
|