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

JRCT ID: jRCTs042190034

Registered date:31/05/2019

Basic Information

• Recruitment status: Complete
• Health condition(s) or Problem(s) studied: volunteer
• Date of first enrollment: 31/05/2019
• Target sample size: 130
• Study type: Interventional

Intervention(s)

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 twice using Shimadzu device, total 3 times on the same day.

Outcome(s)

• Primary Outcome: Bone mineral density, bone mineral content and bone area of lumber vertebra and femur.

Key inclusion & exclusion criteria

• Age minimum: >= 20age old
• Age maximum: Not applicable
• Gender: Both

Include 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.

Exclude 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.

Related Information

• Primary Sponsor: Oguchi Takeshi
• Source(s) of Monetary Support: Shimadzu Corpration