Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06762730

Zoledronic Acid for the Prevention of TDF-sparing ART-induced Bone Mass Density Loss in Treatment-naive HIV Positive Individuals

A Single Dose Intravenous Administration of Zoledronic Acid for the Prevention of TDF-sparing ART-induced Bone Mass Density Loss in Treatment-naive HIV Positive Individuals - a Prospective, Multicenter, Open-label, Randomized Control Trial

Status
Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
110 (estimated)
Sponsor
Hadassah Medical Organization · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this clinical trial is to learn if zolendric acid can prevent the anticipated deterioration of bone mass after antiviral treatment initiation for people that were recently diagnosed with HIV. The main questions it aims to answer are: 1. Is bone mass deterioration is significant even with the new medication currently used to treat HIV? 2. Can one dose of Zolendric acid protect from deterioration of bone mass. Researchers will compare one dose of zolendric acid to follow-up only Participant will: 1. Provide blood samples for bone markers before antiviral treatment initiation and at 6M,12M,24M and 48M after treatment initiation 2. Perform DXA scan soon after antiviral treatment initiation and after 12M ,24 M and 48 months 3. Half of the patients with moderate reduction in bone mass will be treated with one dose of zolendric acid in the clinical trial, the other participants will be followed without intervention. 4. Patients with substantial osteoporosis will be treated according to standard of care by their HMO, but will continue followup in the study.

Conditions

Interventions

TypeNameDescription
DRUGZoledronic Acid 5 mg/Bag 100 ml InjZolendric acid will be provided to HIV naïve patients with documented osteopnia

Timeline

Start date
2024-12-09
Primary completion
2028-12-01
Completion
2032-12-01
First posted
2025-01-08
Last updated
2025-09-18

Locations

3 sites across 1 country: Israel

Source: ClinicalTrials.gov record NCT06762730. Inclusion in this directory is not an endorsement.