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Clinical Outcomes in HIV With Comorbidities

Renal, Metabolic, Hepatic and Bone Outcomes in People Living With HIV and Other Co-morbidities Receiving Different Anti-retroviral Regimens

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05824130
Enrollment
300
Registered
2023-04-21
Start date
2023-04-13
Completion date
2025-10-31
Last updated
2023-08-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hiv

Brief summary

Multi-arm, non-randomized, quality of life

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.

Interventions

None listed

Sponsors

Grace Lui
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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

Design outcomes

Primary

MeasureTime frameDescription
Renal diseasesBaselineRenal 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.
DyslipidemiaBaselineDyslipidemia 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.
Cardiovascular riskBaselineHigh cardiovascular disease risk is defined as QRISK3 \>10%. QRISK3 will be calculated from QRISK 3 risk calculator at qrisk.org.
Liver steatosis and fibrosisBaselineLiver 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.
Low bone mineral densityBaselineLow 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.
Health-related quality of lifeBaselineany 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

MeasureTime frameDescription
Incidences of Comorbidities12 months or at the time of change of ART regimenAll the above endpoints will be determined at 1 year follow up or at the time of change of ART regimen

Countries

Hong Kong

Contacts

Primary ContactCatherine Cheung, Mphil
catherinecheung@cuhk.edu.hk+852 35053376

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026