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Bindex for Osteoporosis Diagnostics

Bindex for Osteoporosis Diagnostics

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03878732
Enrollment
293
Registered
2019-03-18
Start date
2019-03-11
Completion date
2020-02-07
Last updated
2020-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoporosis, Postmenopausal

Brief summary

Osteoporosis is a disease that leads to impaired skeletal strength and increased fracture risk. Among 200 million osteoporotic patients most are diagnosed only after several fractures. Furthermore, the progressively aging population will increase the prevalence of osteoporosis. It is estimated that over 75% of osteoporotic patients are not diagnosed and does not receive treatment for their condition. Bindex ultrasound device has been developed and validated in Caucasian female population. In this study, diagnostic thresholds for density index as determined with Bindex will be evaluated in two different ethnic populations.

Detailed description

Currently, the diagnosis of osteoporosis is based on the measurement of bone mineral density (BMD), using axial dual energy X-ray absorptiometry (DXA) of the hip and/or the lumbar spine at special healthcare. Application of diagnostic thresholds determined against BMD have been suggested by International Society for Clinical Densitometry (ISCD) for use with peripheral bone densitometry devices (90% sensitivity and 90% specificity). These thresholds have been determined and validated for Bindex in Caucasian female population. This study focuses on clinical validation of the ultrasound device (Bindex®, Bone Index Finland Ltd., www.boneindex.com) device and Density Index (DI), a diagnostic parameter reported by Bindex. The predetermined thresholds for DI will be evaluated by measuring 70 osteoporotic and 70 healthy patients with Bindex and DXA in each selected patient groups. The feasibility of DI for diagnostics of osteoporosis in these groups will be assessed.

Interventions

DIAGNOSTIC_TESTBindex measurement

One time bone density measurement with ultrasound device

Sponsors

New Mexico Clincial Research & Osteoporosis Center, Inc.
CollaboratorUNKNOWN
Bone Index Finland Ltd
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
50 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

for all: * Postmenopausal status * Age at 50 years or over * Caucasian or Hispanic race (number shall be controlled, 140 in each group) * Body mass index (BMI \< 35) Additional criteria for Osteoporotic group \- T-Score (NHANES database) -2.5 or lower at femoral neck or total femur Additional criteria for non-osteoporotic group \- T-Score (NHANES database) \> -2.5 at femoral neck or total femur

Exclusion criteria

for non-osteoporotic groups (Hispanic or Caucasian) * Previous osteoporosis diagnosis * Previous or current use of anti-fracture medication

Design outcomes

Primary

MeasureTime frameDescription
Sensitivity and specificity of DI3/11/2019-11/29/2019Sensitivity and specificity of DI in caucasian and hispanic groups

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026