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Clinical Trials in the UK / NCT06151353
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)

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