HIVAIRNCT03501719
Effects of ART Simplification on Inflammatory Markers in CoRis (AIR)
An observational study of HIV, run by Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal at 1 site in Spain.
Trial summary
The effects of the number of drugs included in antiretroviral therapy (ART) regimens of inflammatory markers remains undefined. We will evaluated in participants in the Spanish AIDS Research Network, whether triple ART, dual ART or monotherapy affect differentially the dynamics of inflammatory markers. Read more about this study
- Who is it for?
- Ages 18 to 100 years
- Conditions the study is for
- HIV
- What is being tested?
- Number of drugs in the ART regimen
- How many people
- 177 participants
- Where
- 1 siteSpain
- Study dates
- 1 Mar 2018to 1 Mar 2022
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 100 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: HIV-infected patients
Who may be able to join
- Subjects initiating ART in CoRIS from 2004 with triple therapy.
- HIV RNA suppression achieved in the first 48 weeks of ART.
Who cannot join
- ART initiation with regimens with less than three drugs
- Virologic failure in the first 48 weeks of ART
- AIDS conditions or serious non-AIDS events in the first 48 weeks of ART.
Trial locations and contacts
1 site in 1 country.
About this study
The effects of the number of drugs included in antiretroviral therapy (ART) regimens of inflammatory markers remains undefined. We will evaluated in participants in the Spanish AIDS Research Network, whether triple ART, dual ART or monotherapy affect differentially the dynamics of inflammatory markers.
Read the detailed description
During treated HIV infection, higher levels of the inflammatory and coagulation markers interleukin-6 (IL-6), D-dimers, and high-sensitivity C-reactive protein (hs-CRP) are associated with an increased risk of cardio-vascular disease (CVD), cancer, and all-cause mortality. While ART decreases IL-6, D-dimer and hs-CRP levels, these biomarkers remain elevated relative to the general population even when the plasma HIV RNA is suppressed. Markers of inflammation and coagulation have been widely studied in the general population, and related to higher risk of CVD, cancer, kidney function decline and all-cause mortality. These data collectively suggest that chronic inflammation and/or hyper-coagulation contribute to the pathogenesis of these serious non-AIDS events during otherwise effective ART. Given the assumed, albeit unproven, role of these pathways in causing disease, both vascular and non-vascular, there is intense interest in studying interventions that reduce inflammation and/or coagulation.
Recent simplification strategies have demonstrated that once HIV RNA suppression is achieved, the extent of virological control does not appear to depend so much on the number of drugs, but on the time of HIV RNA suppression before the simplification. In fact, some simplification therapies, including dual regimens based in boosted-protease inhibitors (PI) have proved to be non-inferior to triple ART, provided that drug resistance has been excluded. More recently, dual therapies based in other combinations not based in boosted-PI have emerged as viable therapeutic strategies.
While these approaches of ART simplification seems to be non-inferior to standard triple therapy in terms of short-term plasma HIV RNA suppression and CD4+ T cell count dynamics, it is unknown whether ART simplification will prove safe in the long term. Mounting evidence support that the concentration of drugs, which may be related to the number of drugs, affects the extent of virological control in the tissues in which HIV persists and replicates, generating low-level viremia and contributing to chronic inflammation. It is likely that clinical trials powered to detect differences in clinical events will not be performed. Hence, the long-term clinical efficacy of ART simplification must be assessed in cohort studies and the long-term effects on inflammatory markers that independently predict mortality must be assessed.
- Conditions
- HIV
- Being tested
- Number of drugs in the ART regimen
- Keywords
- HIV, inflammation, antiretroviral therapy, cohort studies, mortality, non-AIDS events
- Medical subject headings
- Inflammation
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Number of drugs in the ART regimenDrug
Triple therapy vs. dual therapy vs. monotherapy
| Study group | Role | What they receive |
|---|---|---|
| Triple ART | Patients who remain in triple ART during the follow-up. Receives: Drug: Number of drugs in the ART regimen | |
| Dual ART | Patients switched to dual ART during the follow-up. Receives: Drug: Number of drugs in the ART regimen | |
| Monotherapy | Patients switched to monotherapy during the follow-up. Receives: Drug: Number of drugs in the ART regimen |
What is being measured
The primary outcome is the main question the study is designed to answer.
Inflammation
Plasma IL-6 levels in plasma
Measured: From baseline through study completion, an average of 3 years
Secondary outcomes (11)
Immune activation
CD4/CD8 ratio in blood
Measured: From baseline through study completion, an average of 3 years
Coagulation
D-dimers levels in plasma
Measured: From baseline through study completion, an average of 3 years
Gut epithelial integrity
Intestinal fatty acid binding protein (IFABP) levels in plasma
Measured: From baseline through study completion, an average of 3 years
Monocyte activation/bacterial translocation
Soluble CD14 levels in plasma
Measured: From baseline through study completion, an average of 3 years
Immunological variables
Nadir CD4+ T cell count, highest CD8+ T cell count and nadir CD4/CD8 ratio.
Measured: From baseline through study completion, an average of 3 years
Comorbidities
Number and type of comorbidities, including HCV coinfection.
Measured: From baseline through study completion, an average of 3 years
Period
Year of ART initiation
Measured: Baseline
ART history
Number of previous ART regimens
Measured: From baseline through study completion, an average of 3 years
Available virological information
Number of HIV RNA determinations
Measured: From baseline through study completion, an average of 3 years
ART exposure
Number and reasons of previous ART modifications
Measured: From baseline through study completion, an average of 3 years
Sociodemographics
Country of origin
Measured: At baseline
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Apr 2018
- Study start1 Mar 2018
- Primary completion1 Mar 2022
- Study completion1 Mar 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for HIVStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Retrospective
- Enrolment
- 177 participants (actual)
Sponsor and investigators
- Lead sponsor
- Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03501719
- Sponsor's protocol ID
- 133-17
- Acronym
- AIR
- Status last verified
- Mar 2025
- First submitted
- 22 Mar 2018
- Last updated
- 17 Mar 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 17 Mar 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effects of ART Simplification on Inflammatory Markers in CoRis (AIR)
- ClinicalTrials.gov ID
- NCT03501719
- Acronym / sponsor ID
- AIR / 133-17
- Conditions
- HIV
- Keywords
- HIV, inflammation, antiretroviral therapy, cohort studies, mortality, non-AIDS events
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 177 participants (actual)
- Lead sponsor
- Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y CajalUniversity, hospital or other
- Study start
- 1 Mar 2018 (actual)
- Primary completion
- 1 Mar 2022 (actual)
- Study completion
- 1 Mar 2022 (actual)
- First posted
- 18 Apr 2018 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The effects of the number of drugs included in antiretroviral therapy (ART) regimens of inflammatory markers remains undefined. We will evaluated in participants in the Spanish AIDS Research Network, whether triple ART, dual ART or monotherapy affect differentially the dynamics of inflammatory markers.
Detailed description
During treated HIV infection, higher levels of the inflammatory and coagulation markers interleukin-6 (IL-6), D-dimers, and high-sensitivity C-reactive protein (hs-CRP) are associated with an increased risk of cardio-vascular disease (CVD), cancer, and all-cause mortality. While ART decreases IL-6, D-dimer and hs-CRP levels, these biomarkers remain elevated relative to the general population even when the plasma HIV RNA is suppressed. Markers of inflammation and coagulation have been widely studied in the general population, and related to higher risk of CVD, cancer, kidney function decline and all-cause mortality. These data collectively suggest that chronic inflammation and/or hyper-coagulation contribute to the pathogenesis of these serious non-AIDS events during otherwise effective ART. Given the assumed, albeit unproven, role of these pathways in causing disease, both vascular and non-vascular, there is intense interest in studying interventions that reduce inflammation and/or coagulation.
Recent simplification strategies have demonstrated that once HIV RNA suppression is achieved, the extent of virological control does not appear to depend so much on the number of drugs, but on the time of HIV RNA suppression before the simplification. In fact, some simplification therapies, including dual regimens based in boosted-protease inhibitors (PI) have proved to be non-inferior to triple ART, provided that drug resistance has been excluded. More recently, dual therapies based in other combinations not based in boosted-PI have emerged as viable therapeutic strategies.
While these approaches of ART simplification seems to be non-inferior to standard triple therapy in terms of short-term plasma HIV RNA suppression and CD4+ T cell count dynamics, it is unknown whether ART simplification will prove safe in the long term. Mounting evidence support that the concentration of drugs, which may be related to the number of drugs, affects the extent of virological control in the tissues in which HIV persists and replicates, generating low-level viremia and contributing to chronic inflammation. It is likely that clinical trials powered to detect differences in clinical events will not be performed. Hence, the long-term clinical efficacy of ART simplification must be assessed in cohort studies and the long-term effects on inflammatory markers that independently predict mortality must be assessed.
Study design
- Observational model
- Cohort
- Time perspective
- Retrospective
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Triple ART | – | Drug: Number of drugs in the ART regimenPatients who remain in triple ART during the follow-up. |
| Dual ART | – | Drug: Number of drugs in the ART regimenPatients switched to dual ART during the follow-up. |
| Monotherapy | – | Drug: Number of drugs in the ART regimenPatients switched to monotherapy during the follow-up. |
Who may qualify
- Ages
- 18 to 100 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- HIV-infected patients
Key inclusion criteria (2 listed)
- Subjects initiating ART in CoRIS from 2004 with triple therapy.
- HIV RNA suppression achieved in the first 48 weeks of ART.
Key exclusion criteria (3 listed)
- ART initiation with regimens with less than three drugs
- Virologic failure in the first 48 weeks of ART
- AIDS conditions or serious non-AIDS events in the first 48 weeks of ART.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Number of drugs in the ART regimenTriple therapy vs. dual therapy vs. monotherapy | Drug | Dual ART, Monotherapy, Triple ART |
Primary outcome
Inflammation
Time frame: From baseline through study completion, an average of 3 years
Plasma IL-6 levels in plasma
11 secondary outcomes
Immune activation
Time frame: From baseline through study completion, an average of 3 years
Coagulation
Time frame: From baseline through study completion, an average of 3 years
Gut epithelial integrity
Time frame: From baseline through study completion, an average of 3 years
Monocyte activation/bacterial translocation
Time frame: From baseline through study completion, an average of 3 years
Immunological variables
Time frame: From baseline through study completion, an average of 3 years
Comorbidities
Time frame: From baseline through study completion, an average of 3 years
Period
Time frame: Baseline
ART history
Time frame: From baseline through study completion, an average of 3 years
Available virological information
Time frame: From baseline through study completion, an average of 3 years
ART exposure
Time frame: From baseline through study completion, an average of 3 years
Sociodemographics
Time frame: At baseline
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Mar 2025.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of HIV, run by Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal at 1 site in Spain.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 17 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Inflammation (time frame: From baseline through study completion, an average of 3 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Mar 2025.