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Not yet recruiting NCT06513442

The Added Value of Bone Microstructure Assessment in the Management of Osteoporotic Bone

Observational Osteoporosis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Trabecular bone score software.
Who it may be relevant to
Registry conditions: Osteoporosis. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

1. To assess the clinical utility of trabecular bone score (TBS) on fracture risk prediction including the new version (TBS V4) and future TBS versions at the spine and hip. 2. To assess the clinical utility of TBS software as a potential treatment outcome: sensitivity to change over time and following osteoporosis therapy. 3. To compare TBS to other imaging modalities of bone structure such as quantitative computed tomography (QCT) in fracture risk prediction and response to osteoporosis therapy.

Interventions

  • Other Trabecular bone score software
    To assess the clinical utility of trabecular bone score (TBS) on fracture risk prediction including the new version (TBS V4) and future TBS versions at the spine and hip.

Primary outcome measures

  • To assess the newest version of TBS software on fracture prediction [Time frame: 10 years]

Eligibility criteria

Inclusion Criteria: Has had a DEXA scan

  • Has had a DEXA scan

Exclusion criteria

  • Unable to complete DEXA scan

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06513442 · 1.1

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗