On-Body Passive-RFID Antenna Array and Testbed to Assess Changes in Bone Structure
On-Body Passive-RFID Antenna Array and Testbed to Assess Changes in Bone Structure
批准号:
9406456
负责人:
Sergey N Makaroff
金额:
$22.48万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-08-01 至 2019-01-31
关键词:
AffectAmericanAnatomyBone DensityBone structureBostonCadaverDetectionDevicesDisadvantagedDoseDual-Energy X-Ray AbsorptiometryFractureFrequenciesGoalsHazardous SubstancesHealthHealth Care CostsImageIndividualIonizing radiationIonsIsraelLegal patentManualsManufacturer NameMeasurementMeasuresMedicalMethodsModernizationNoiseOrthopedicsOsteopeniaOsteoporosisOsteoporoticPatientsPhasePhysiologicalPilot ProjectsProductionProtocols documentationRadiologic HealthReaderReadingSaint Jude Children&aposs Research HospitalSamplingSideSignal TransductionSkinSurfaceTechniquesTechnologyTestingTissuesUnited States Dept. of Health and Human ServicesUnited States Food and Drug AdministrationVariantWorld Health OrganizationWristX-Ray Computed Tomographybasebonecortical bonecostdesigndesign and constructiondigitalfracture riskin vivomicrowave electromagnetic radiationnovelosteoporotic bonepressureradio frequencysoft tissuesubstantia spongiosayoung adult
中文摘要
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英文摘要
PROJECT SUMMARY/ABSTRACT
More than 10 million Americans have osteoporosis, and an additional 36 million have low bone density, or
osteopenia. Osteoporosis represents a major health problem, resulting in substantial increases in national
health care costs. Current methods to detect osteoporosis rely upon ionizing techniques such as Dual-energy
X-ray Absorptiometry (DXA) and Quantitative Computed Tomography (QCT). A pilot study conducted by our
collaborators indicated a possible correlation between readings of an array of passive on-skin 900 MHz Radio
Frequency Identification (RFID) tags surrounding a wrist and an osteoporotic bone condition established via
DXA measurements. We therefore hypothesize that a professional acquisition testbed, using this novel low-
cost non-ionizing technique, can detect osteoporosis.
Specific Aim 1 (PHASE I): Design and construct a novel on-body passive-RFID antenna array testbed
for highly-sensitive and repeatable measurements of wrist bone signature. In contrast to a common
microwave imaging setup with multiple antennas, the use of an RFID array instead of one tag is solely
intended for more accurate and stable reading of the single parameter – the average received power through
the wrist – given different anatomical and physiological conditions.
Specific Aim 2 (PHASE I): Determine the sensitivity of the bone signature measured by the testbed
for differentiating between normal and osteoporotic bones at wrists using in-vivo pilot studies. The
ultimate technical goal of Phase I (and partially of Phase II) is to achieve a sufficient measurement accuracy of
the testbed, i.e. guarantee the average received power variability for each wrist of less than 0.5 dB (factor of
1.1) for at least 75% of tested wrists. This threshold value will make it possible to extract the desired signal
from the surrounding noise and detect the osteoporosis-related power variation, which is expected to be in the
range 2-5 dB (factor of 1.6-3.2).
Specific Aim 1 (PHASE II): Finalize the major antenna concepts and protect the RFID antenna bone
density testbed by filing at least one full-scale patent with the special emphasis on the unique
reader/tag antenna array design, and on possible extensions. Convert the RFID antenna testbed to a
semi-commercial product. One feature of the present study will be a novel and unique on-body antenna
design, which will allow us to realize a highly-sensitive detection method in practice.
Specific Aim 2 (PHASE II): Calibrate the finalized RFID antenna testbed by performing and
processing a representative in-vivo study and delivering a final detection protocol. Finalize and
perform premarket regulatory submission of the developed wrist sensing RFID device to the U.S.
Department of Health and Human Services, Food and Drug Administration, Center for Devices and
Radiological Health. We hypothesize that the newly designed testbed will differentiate between normal,
osteopenic and osteoporotic bone sufficiently to warrant a premarket regulatory FDA submission related to a
specific Class III device.
Specific Aim 3 (PHASE II): Approach the production stage by either teaming up with a larger medical
company or a 3rd party manufacturer. Potential candidates include Biotronik, Boston Scientific, St. Jude
Medical, Inc. and Medtronic, Inc.
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