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Enrolling by invitation Observational

Performance of REMS Bone Densitometry in a British Population

NCT06151353 · tracked via the Priya Life Science UK tracker
Sponsor
OsteoscanUK Ltd
Phase
Observational
Started
2023-11-21
Last updated
2025-08-17

Condition(s) studied

Bone Densitometry

Investigational drug(s) / intervention(s)

REMS

REMS: Bone health assessment using REMS, an ultrasound technology developed to measure bone mineral density and bone toughness without ionising radiation

Study summary

Radiofrequency echographic multispectrometry (REMS) is a recently developed technology that uses ultrasound to assess bone density and bone quality. It was launched in 2018 since when OsteoscanUK Ltd has offered a clinical bone health service using a REMS scanner. REMS is an alternative to x-ray based dual energy x-ray absorptiometry (DEXA) scans which are considered the "Gold Standard" for clinical densitometry. REMS is unique in offering not only bone density but also bone quality assessments in real time for both the spine and hip.

Eligibility

Sex
FEMALE
Min age
20 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * All women over the age of 20 years presenting for a REMS scan Exclusion Criteria: * Lack of consent for the procedure and for the anonymised data to be stored and used for research; Previous bilateral total hip replacements; un controlled spasticity following a neurological injury of development of a neurodegenerative condition

Primary outcome measure(s)

  • Longitudinal assessment of the change in bone mineral density (BMD) and bone toughness (Fragility Score) and correlation with fragility fracture status, age, menopausal status and body mass index, — 5 years for collection of sufficient data for meaningful analysis
    Analysis of the change in bone health parameters measured by REMS from the start of the study until final follow-up which will be at least 24 months

Trial sites (1)

FacilityCityRegionStatus
Bragborough Hall Health Centre Daventry Northamptonshire
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06151353 on ClinicalTrials.gov ↗ ← All trials in the UK