- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05424536
Cortical Bone Assessment Using Ultrasonic Guided Waves: Towards a Robust Clinical Measurement (BDATChile)
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
Conditions
Intervention / Treatment
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
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Valparaíso, Chile
- Universidad de Valparaiso
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
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
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
Sponsor
Collaborators
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
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1201311
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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