RecruitingPhase 4NCT07406685

The Comparison of Ibandronate and Zoledronic Acid After Denosumab Discontinuation

The Comparison of Ibandronate and Zoledronic Acid After Denosumab Discontinuation: A Randomized Non-inferiority Trial


Sponsor

National Taiwan University Hospital

Enrollment

52 participants

Start Date

Aug 20, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This study is a prospective, multicenter, open-label, randomized non-inferiority trial comparing intravenous ibandronate and zoledronic acid as sequential therapy after denosumab discontinuation in postmenopausal women with osteoporosis. This trial primarily targets patients with short-term denosumab exposure (less than three years) and is conducted as a preliminary investigation. The findings are expected to provide foundational evidence to inform the design of future studies assessing sequential therapies following longer-term denosumab treatment.


Eligibility

Sex: FEMALEMin Age: 50 YearsMax Age: 85 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Ibandronate IV and a drug called Zoledronic acid IV for people with osteoporosis, postmenopausal osteopenia, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include women aged 50 Years to 85 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGIbandronate IV

Ibandronate 3mg/3months for 12 months

DRUGZoledronic acid IV

Zoledronic acid 5mg/1year for 12 months


Locations(1)

National Taiwan University Hospital

Taipei, Taiwan

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NCT07406685


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