Alendronate for Prevention of AntiRetroviral Therapy-associated Bone Loss (APART)
Status and phase
Conditions
Treatments
Details and patient eligibility
About
Antiretroviral therapy (ART) initiation is associated with a significant loss of bone mineral density (BMD), characterised by increases in bone turnover, which is largely limited to the first 48 weeks of therapy. Bisphosphonates, such as alendronate, decrease bone turnover and can limit loss of bone mineral density.
This study aims to determine if a short course of treatment with the oral bisphosphonate alendronate can limit loss of bone mineral density associated with initiation of ART in HIV-1 infected, antiretroviral naive, adult subjects.
Full description
Multi-centre, prospective, randomised, double-blind, placebo-controlled trial over 50 weeks. The aims of this study include:
- To determine if short-course treatment with alendronate versus placebo combined with calcium and vitamin D, initiated 2 weeks prior to start of ART and can prevent loss of BMD over 48 weeks of follow-up post ART initiation.
- To explore the effect of alendronate on bone turnover in the setting of ART initiation.
- To determine which factors, such as choice of ART, impacts the protective effect of alendronate in preventing BMD loss.
- To determine the relationship between changes in bone turnover markers, vitamin D, parathyroid hormone and calcium levels.
- To explore the pathogenesis of BMD loss with initiation of ART by investigating relationships between changes in immune function (T-cells and B-cells subsets), bone turnover and BMD.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- male>30 years old or female>35 years old
- HIV-1 antibody positive
- antiretroviral therapy naïve
- be presumed to have achieved peak bone mass
- be eligible for initiation of antiretroviral therapy in the opinion of the investigator
- be able to provide written, informed consent
Exclusion criteria
- subjects unable to comply with the study protocol or unable to stand/sit upright for at least 30 minutes
- history of osteoporosis
- history of fragility fracture or previous femoral fracture
- chronic renal failure
- hypocalcemia or hypercalcemia at screening
- history of Paget's disease or known primary hyperparathyroidism
- previous treatment with or allergy (including hypersensitivity) to bisphosphonates
- recent history (past 12 months) of peptic or duodenal ulcers or oesophagitis, aspiration or any other abnormality of the oesophagus
- current therapy with prescribed calcium or vitamin D preparations (other than over-the-counter multivitamin preparations)
- current therapy with aspirin or other regularly prescribed non-steroidal anti-inflammatory drugs
- recent dental work (within the past 3 months) or poor oral hygiene (as judged in the opinion of the investigator)
- recent (within the past three months) significant steroid exposure
- for female subjects: pregnancy at screening, planning future pregnancies or unwilling to take measures to avoid pregnancy for the duration of the study
- where in the investigator's opinion, there is a necessity to initiate ART within the pre-ART study window period
- hepatitis B or hepatitis C co-infection
- any active illness (including AIDS illness) which in the opinion of the investigator precludes participation in the study
- subjects concurrently enrolled in another clinical trial of an investigational medical product
Trial design
Primary purpose
Allocation
Interventional model
Masking
53 participants in 2 patient groups, including a placebo group
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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