Clinical Outcomes in HIV With Comorbidities

Sponsor
Grace Lui (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05824130
Collaborator
(none)
300
30

Study Details

Study Description

Brief Summary

Multi-arm, non-randomized, quality of life

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This is a prospective, longitudinal, observational study, performed at a Co-morbidities clinic for PLWH. PLWH with one or more co-morbidities receiving anti-retroviral therapy (ART) will be analyzed for their prevalence and incidence of developing renal, metabolic, hepatic and bone diseases. All participants will be assessed at baseline and followed up for one year, or until change in ART regimen, whichever earlier.

    Study Design

    Study Type:
    Observational [Patient Registry]
    Anticipated Enrollment :
    300 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Renal, Metabolic, Hepatic and Bone Outcomes in People Living With HIV and Other Co-morbidities Receiving Different Anti-retroviral Regimens
    Anticipated Study Start Date :
    May 1, 2023
    Anticipated Primary Completion Date :
    Oct 31, 2025
    Anticipated Study Completion Date :
    Oct 31, 2025

    Arms and Interventions

    Arm Intervention/Treatment
    B/F/TAF group

    B/F/TAF

    other INSTI-based ART regimen

    1-2 NRTI(s) plus an INSTI other than bictegravir

    non-INSTI-based ART regimen

    2 NRTIs plus NNRTI or protease inhibitor

    Outcome Measures

    Primary Outcome Measures

    1. Renal diseases [Baseline]

      Renal disease is defined as glomerular filtration rate (GFR) <60 mL/min/1.73m2, or presence of albuminuria, defined as urine albumin:creatinine >3 mg/mmol, according to Kidney Disease Improving Global Outcomes (KDIGO) categorization of chronic kidney disease. Blood will be taken for creatinine and urine for creatinine and albumin levels.

    2. Dyslipidemia [Baseline]

      Dyslipidemia is defined as total cholesterol >5.17 mmol/l, triglyceride >1.7 mmol/l, HDL cholesterol <1.03 mmol/l in men and <1.29 mmol/l in women, or LDL cholesterol >4.1 mmol/l, or a history of taking anti-hyperlipidemic drugs, according to the National Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (ATP III) guidelines. Fasting blood sample will be taken to measure total, LDL and HDL cholesterol and triglyceride levels.

    3. Cardiovascular risk [Baseline]

      High cardiovascular disease risk is defined as QRISK3 >10%. QRISK3 will be calculated from QRISK 3 risk calculator at qrisk.org.

    4. Liver steatosis and fibrosis [Baseline]

      Liver steatosis is defined as Controlled Attenuated Parameter (CAP) >248 dB/m and significant fibrosis is defined as liver stiffness >9.0 kPa, as measured by transient elastography. Transient elastography will be performed to measure CAP and liver stiffness.

    5. Low bone mineral density [Baseline]

      Low bone mineral density is defined as T score <-1.0 in men 50 years and in post-menopausal women at either lumbar spine or femoral neck, and Z score <-2.0 in men younger than 50 years and pre-menopausal women, as measured by dual energy X-ray absorptiometry (DXA). DXA scan will be performed to measure bone mineral density at lumbar spine and femoral neck.

    6. Health-related quality of life [Baseline]

      any severity of problem in the five dimensions of EQ-5D-5L, EQ-5D-5L index and EQ-VAS EuroQol 5 level EQ-5D version will be performed to measure the above parameters.

    Secondary Outcome Measures

    1. Incidences of Comorbidities [12 months or at the time of change of ART regimen]

      All the above endpoints will be determined at 1 year follow up or at the time of change of ART regimen

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. HIV antibody positive

    2. Age above 18 years

    3. Diagnosis of one or more co-morbidities, including hypertension, diabetes, dyslipidemia, chronic kidney disease, chronic liver disease, and cardiovascular diseases

    4. Receiving ART regimen, which consists of B/F/TAF, or 1-2 NRTI(s), plus another anti-retroviral drug, including INSTI other than bictegravir, NNRTI, or protease inhibitor

    Exclusion Criteria:
    1. Recent diagnosis of AIDS within 6 months

    2. Recent hospitalization for management of acute medical problems within 6 months

    3. Receiving ART regimens other than the combinations listed in Inclusion Criteria

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Grace Lui

    Investigators

    • Principal Investigator: Grace Lui, Chinese University of Hong Kong

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Grace Lui, Honorary Clinical Associate Professor, Chinese University of Hong Kong
    ClinicalTrials.gov Identifier:
    NCT05824130
    Other Study ID Numbers:
    • HIV ART study
    First Posted:
    Apr 21, 2023
    Last Update Posted:
    Apr 21, 2023
    Last Verified:
    Apr 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No

    Study Results

    No Results Posted as of Apr 21, 2023