Cortical Bone Assessment Using Ultrasonic Guided Waves: Towards a Robust Clinical Measurement (BDATChile)

January 14, 2026 updated by: Universidad de Valparaiso

Cortical Bone Assessment Using Ultrasonic Guided Waves: Towards a Robust Clinical

Osteoporosis is a skeletal disease leading to bone fragility and increasing the risk of fractures and still remains a major public health problem worldwide. Therefore it is crucial to prevent severe fractures responsible for excess of mortality and considerable morbidity. Patient at risk of fractures are currently identified as having osteoporosis using Dual-energy X-ray Absorptiometry (DXA), assessing the areal or projected Bone Mineral Density (aBMD g.cm-2). In Chile, the hip fracture occurrence is very similar to the international incidence. Due to the demographic and epidemiological transition, the number of hip fracture for patient older than 50 year, is expected to severely increase from about 6.500 (2007) to 30.000 (2050) without adequate preventive and / or therapeutic measures.

Even if DXA remains the current gold standard, it is limited by the difficulty to set a threshold in the BMD distribution for osteoporosis diagnosis. Moreover, some medical conditions (chronic kidney disease, diabetes) or drugs (glucocorticoids) are associated with an increase of fracture risk without a BMD decrease. Quantitative ultrasound (QUS) have the advantages of portability, low cost, absence of radiation and need for a radiographic technologist or designated room, and are sensitive to both elasticity and geometry of the medium explored by the waves. Among QUS techniques, axial transmission (AT) is a technique for which transducers are aligned along the bone axis. Measured ultrasonic guided waves, associated with an appropriate waveguide model have the potential to yield estimates of material and/or geometrical cortical properties. In vivo combined estimation of both cortical thickness and porosity has been proposed using bidirectional axial transmission (BDAT). BDAT measurement has been recently validated on ex vivo specimen (radius and tibia) and has been tested in a pilot clinical study, in which cortical porosity measured at the one-third distal radius has been found as discriminant of low trauma fractures as DXA. Cortical porosity is increasingly recognized as a major contributor to bone fragility.

The hypothesis underlying this project are that (1) it is possible to obtain robust and accurate estimates of cortical thickness and porosity using an improved BDAT device and (2) these estimates are of clinical interest in the context of osteoporosis in elderly. Moreover, novel parameters obtained from automatic classification tools will be tested.

Study Overview

Status

Completed

Detailed Description

The purpose of this investigation is to determine if there are differences in the quantities of cortical bone (thickness and porosity) as well as the new parameters measured by BDAT at both forearm and leg, between patients with recent non traumatic fracture and controls.

Results will be compared to the current gold standard dual-energy X-ray absorptiometry (DXA) of the hip, spine and forearm, obtained from all subjects. The BDAT device with the improved interface will be tested in a clinical environment by clinical operators on:

  • minimum sample size per group: 25 for cases and controls (female and male, over 50 years).
  • Fractured patients will be obtained at the traumatology service of Fricke Hospital (Viña del Mar) which receives about 350 patients with hip fractures per year.
  • Control will be obtained at the community health centers of Valparaiso in collaboration with the UV project Geropolis.

DXA measurement will be done at the imaging center of the Universidad Catolica de Valparaiso (PUCV, FONDEQUIP EQM160142). Additional DXA parameters concerning muscle and fat, will be taken into account.

Study Type

Observational

Enrollment (Actual)

50

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Valparaíso, Chile
        • Universidad de Valparaiso

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

50 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

The cohort will be:

Women and men over 50 years old

Description

For both groups:

Inclusion Criteria:

  • > 50 years old

Exclusion Criteria:

  • History of fracture
  • Corticoid treatment
  • Renal disease
  • Arthritis
  • BMI < 15 and > 30
  • Double femoral prosthesis

In case group/with fracture is added:

Inclusion criteria

  • Recent femoral bone fragility fracture

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Cortical parameter measurement obtained by BDAT (Ultrasound)
Time Frame: Inclusion time
Cortical thickness (mm) at one-third distal radius and mid-tibia
Inclusion time
Cortical parameter measurement obtained by BDAT (Ultrasound)
Time Frame: Inclusion time
Cortical porosity (%) at one-third distal radius and mid-tibia
Inclusion time
Ultrasonic velocities measurement obtained by BDAT (Ultrasound)
Time Frame: Inclusion time
velocity (m.s-1) of the First Arriving Signal (VFAS) at one-third distal radius and mid-tibia
Inclusion time
Ultrasonic velocities measurement obtained by BDAT (Ultrasound)
Time Frame: Inclusion time
velocity (m.s-1) of the A0 guided mode (A0) at one-third distal radius and mid-tibia
Inclusion time

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Quality measurement parameter obtained by BDAT (Ultrasound)
Time Frame: Inclusion time
measurement at one-third distal radius and mid-tibia, normalized quality parameter (value ranging from 0 to 1).
Inclusion time
femoral aBMD obtained by DXA
Time Frame: Inclusion time
measurement of femoral areal Bone Mineral Density (aBMD g.cm-2).
Inclusion time
Body composition measurements obtained by DXA
Time Frame: Inclusion time
body composition: body fat, muscle and bone mass (kg).
Inclusion time
10-year probability of fracture provided by FRAX algotithm
Time Frame: Inclusion time
10-year probability of a major osteoporotic fracture, calculated with the femoral aBMD value.
Inclusion time
10-year probability of fracture provided by FRAX algotithm
Time Frame: Inclusion time
10-year probability of a major osteoporotic fracture, calculated without the femoral aBMD value.
Inclusion time

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Jean-Gabriel Minonzio, Ph.D, Universidad de Valparaiso
  • Study Chair: José Luis Dinamarca, M.D., Universidad de Valparaiso

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 18, 2022

Primary Completion (Actual)

January 24, 2023

Study Completion (Actual)

January 31, 2024

Study Registration Dates

First Submitted

June 14, 2022

First Submitted That Met QC Criteria

June 14, 2022

First Posted (Actual)

June 21, 2022

Study Record Updates

Last Update Posted (Estimated)

January 16, 2026

Last Update Submitted That Met QC Criteria

January 14, 2026

Last Verified

January 1, 2023

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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