Clinical study to research correlation of bone mineral density between Shimadzu DXA device and GE DXA device.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-jRCTs042190034

Enrollment

130

Registered

2019-05-31

Start date

2019-05-31

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

volunteer

Interventions

For subjects in this study, we measure bone density in the each Shimadzu device and GE device once on the same day. Still for part of all subjects, we measure bone density once using GE device and twi

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1)The person whose is age 20 years old or more.(Regardless of gender) 2)The person who can understand this study and sign the consent form of this study by authentic signature.

Exclusion criteria

Exclusion criteria: 1)The persons who is not suitable for the measurement of DXA, for example, the person with the vertebral fracture past or proximal femur fracture past in measurement range(L1-L4), the person who has salient scoliosis, and who has fixtures in the body such as metal pin, wire, screw, plate, implant. 2)Pregnant or the persons who may be pregnant. 3)The persons who the investigator or subinvestigator determine unsuitable for participation.

Design outcomes

Primary

Measure	Time frame
Bone mineral density, bone mineral content and bone area of lumber vertebra and femur.	—

Contacts

Public ContactKoji Oda

Anjo Kosei Hospital

oda@kosei.anjo.aichi.jp+81-566-75-2111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026