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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.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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.

Spain1 site
  • Hospital Ramón y Cajal

    Madrid, 28034

Other trials in Spain

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 groups in NCT03501719
Study groupRoleWhat they receive
Triple ARTPatients who remain in triple ART during the follow-up.
Receives: Drug: Number of drugs in the ART regimen
Dual ARTPatients switched to dual ART during the follow-up.
Receives: Drug: Number of drugs in the ART regimen
MonotherapyPatients 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.

  1. Inflammation

    Plasma IL-6 levels in plasma

    Measured: From baseline through study completion, an average of 3 years

Secondary outcomes (11)
  1. Immune activation

    CD4/CD8 ratio in blood

    Measured: From baseline through study completion, an average of 3 years

  2. Coagulation

    D-dimers levels in plasma

    Measured: From baseline through study completion, an average of 3 years

  3. Gut epithelial integrity

    Intestinal fatty acid binding protein (IFABP) levels in plasma

    Measured: From baseline through study completion, an average of 3 years

  4. Monocyte activation/bacterial translocation

    Soluble CD14 levels in plasma

    Measured: From baseline through study completion, an average of 3 years

  5. 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

  6. Comorbidities

    Number and type of comorbidities, including HCV coinfection.

    Measured: From baseline through study completion, an average of 3 years

  7. Period

    Year of ART initiation

    Measured: Baseline

  8. ART history

    Number of previous ART regimens

    Measured: From baseline through study completion, an average of 3 years

  9. Available virological information

    Number of HIV RNA determinations

    Measured: From baseline through study completion, an average of 3 years

  10. ART exposure

    Number and reasons of previous ART modifications

    Measured: From baseline through study completion, an average of 3 years

  11. 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.

  1. First posted18 Apr 2018
  2. Study start1 Mar 2018
  3. Primary completion1 Mar 2022
  4. Study completion1 Mar 2022

Resources

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)
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

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.

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