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NCT03483584Completed

Incidence of HANA Conditions in HIV-infected Individuals

A Prospective Longitudinal Cohort Study to Determine the Incidence of HIV-associated Non-AIDS Conditions in Newly Diagnosed HIV-infected Individuals Initiating Integrase Inhibitor-based and Other Anti-retroviral Regimens

Source: ClinicalTrials.gov · Last updated 9 Dec 2025

Brief summary (registry, in English)

With the availability of effective anti-retroviral therapy, HIV-infected individuals are expected not to die of AIDS and have longer life expectancy. But at the same time, HIV-associated non-AIDS (HANA) conditions are becoming more important in their clinical management. It is currently uncertain whether patients started on different anti-retroviral regimens will have different incidence of HANA conditions. This study aims to evaluate the incidence of various HANA conditions in a cohort of newly diagnosed HIV-infected individuals in Hong Kong initiating anti-retroviral treatment. The incidence of various HANA conditions will be evaluated for those receiving INSTI versus other non-INSTI-based regimens. The HANA conditions evaluated will include 1. Hypertension 2. Diabetes and insulin resistance 3. Dyslipidemia 4. Lipodystrophy 5. Metabolic syndrome 6. Osteopenia and osteoporosis 7. Vitamin D deficiency 8. Renal impairment and kidney tubular dysfunction and 9. Liver fibrosis. Patients will be assessed prior to initiation of anti-retroviral therapy, and 48 weeks and 96 weeks after initiation of treatment. The incidence of development of each HANA condition will be determined and compared between those initiated different anti-retroviral regimens.

Status (registry)
Completed
Study type
Observational
Enrollment
215 (actual)
First submitted
25 Mar 2018
Start date
6 Apr 2018
Primary completion date
31 Mar 2024
Lead sponsor
Chinese University of Hong Kong
Diseases
HIV, Osteoporosis
NCT number
NCT03483584

What you commit to

  • Study type: Observational
  • Participants enrolled: 215
  • From 6 Apr 2018 to the primary completion date, 31 Mar 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Pregnancy
  • Unable to give informed consent

Who the study is looking for

  • Confirmed HIV infection by HIV antibody or RNA test
  • Age ≥18 years old
  • Anti-retroviral treatment naïve
  • Agree to initiate anti-retroviral therapy (ART) as determined by in-charge HIV physician

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Prince of Wales Hospital
Coordinator of this site? Confirm its status
ShatinHong Kong SAR ChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.