Evaluation of Agreement Between CT Scan and 3D-DXA Measurements on the Lombar Spine

Centre Hospitalier Universitaire de Nīmes1 site in 1 country120 target enrollmentFebruary 26, 2019

ConditionsBone Fracture

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: Bone Fracture
Sponsor: Centre Hospitalier Universitaire de Nīmes
Enrollment: 120
Locations: 1
Primary Endpoint: Concordance in lombar spine measurements between box 3D-DXA (index test) and CT scan (reference test)
Status: Active, not recruiting
Last Updated: 3 years ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

Dual-energy X-ray Absorptiometry is frequently used to measure bone mineral density. A new medical device, Box 3D DXA, creates a 3D image using a statistics reconstruction model developed on the femur. This new imaging technique does not require additional irradiation and ought to improve bone measures as well as incorporating densitometric parameters into the diagnosis. This study will test the reconstruction of the 3D image from lombar spine measurements and compare accuracy against measurements made using CT scan.

Registry

clinicaltrials.gov

Start Date

February 26, 2019

End Date

December 2022

Last Updated

3 years ago

Study Type

Interventional

Study Design

Parallel

Sex

All

Investigators

Sponsor

Centre Hospitalier Universitaire de Nīmes

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•The patient must have given their free and informed consent and signed the consent form
•The patient must be a member or beneficiary of a health insurance plan
•The patient is at least 18 years old
•The patient has been referred by a doctor for a PET/CT (Positron Emission Tomography-Computed Tomography) scan or a SPECT (Single Photon Emission Computed Tomography) scan in the Nuclear Medicine and Medical Biophysics Department of Nimes hospital or a bone scan including a SPECT/CT (single photon emission computed tomography coupled with a CT scan)

Exclusion Criteria

•The subject is participating in an interventional study, or is in a period of exclusion determined by a previous study
•The subject refuses to sign the consent
•It is impossible to give the subject informed information
•The patients is under judicial protection or state guardianship
•The patient is pregnant or breast feeding
•The subject has a observably serious scoliosis
•Subject has previously had spinal or hip surgery
•Subject weighs more than 200kg and/or is more than 2 meters tall by 5+65cm wide and 70cm diameter
•Patient uses an insulin pump or wears an insulin or morphine tubing or any attenuating equipment affecting the hips or lumbar spine
•Subject has already had an X-ray exam using a contrast product such as barium in the 7 days preceding the visit

Outcomes

Primary Outcomes

Concordance in lombar spine measurements between box 3D-DXA (index test) and CT scan (reference test)

Time Frame: Day 0

Bland Altman plot

Secondary Outcomes

Robustness of 3D-DXA Femur measurement for femur measurements(Day 0)
Robustness of 3D-DXA Spine measurement for lombar spine measurements(Day 0)
Reproducibility of the 3D-DXA Femur algorithm for femur measurements(Day 0)
Reproducibility of the 3D-DXA Spine algorithm for lombar spine measurements(Day 0)
Concordance in femur measurements between box 3D-DXA (index test) and CT scan (reference test)(Day 0)