Bone Fracture Clinical Trial
— 3D DXA SPINEOfficial title:
Evaluation of Agreement Between CT Scan and 3D-DXA Measurements on the Lombar Spine
Verified date | September 2022 |
Source | Centre Hospitalier Universitaire de Nimes |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Active, not recruiting |
Enrollment | 120 |
Est. completion date | December 2022 |
Est. primary completion date | August 20, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | 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 - Subject having undergone ? radiation exam in the 15 days preceding the visit |
Country | Name | City | State |
---|---|---|---|
France | CHU Nimes | Nîmes |
Lead Sponsor | Collaborator |
---|---|
Centre Hospitalier Universitaire de Nimes | DMS Apelem |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Concordance in lombar spine measurements between box 3D-DXA (index test) and CT scan (reference test) | Lin's concordance coefficient | Day 0 | |
Primary | Concordance in lombar spine measurements between box 3D-DXA (index test) and CT scan (reference test) | Bland Altman plot | Day 0 | |
Secondary | Reproducibility of the 3D-DXA Spine algorithm for lombar spine measurements | 2 acquisitions under the same conditions. Using root-mean-square coefficient of variation to calculate the Least Significant Change | Day 0 | |
Secondary | Robustness of 3D-DXA Spine measurement for lombar spine measurements | 2 acquisitions under the same conditions. Using interquartile range as a measure of dispersion of the variable | Day 0 | |
Secondary | Concordance in femur measurements between box 3D-DXA (index test) and CT scan (reference test) | Lin's concordance coefficient | Day 0 | |
Secondary | Concordance in femur measurements between box 3D-DXA (index test) and CT scan (reference test) | Bland Altman plot | Day 0 | |
Secondary | Reproducibility of the 3D-DXA Femur algorithm for femur measurements | 2 acquisitions under the same conditions. Using root-mean-square coefficient of variation to calculate the Least Significant Change | Day 0 | |
Secondary | Robustness of 3D-DXA Femur measurement for femur measurements | 2 acquisitions under the same conditions. Using interquartile range as a measure of dispersion of the variable | Day 0 |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT06344650 -
Cellular, Molecular and Clinical Determinants of Bone Strength in in Vivo and Human Models of GH Excess. Cross-sectional and Prospective Study
|
||
Recruiting |
NCT02692092 -
HealthEast Community Hip and Knee Replacement Registry
|
N/A | |
Recruiting |
NCT06051682 -
Optimization of the Diagnosis of Bone Fractures in Patients Treated in the Emergency Department by Using Artificial Intelligence for Reading Radiological Images in Comparison With Traditional Reading by the Emergency Doctor.
|
N/A | |
Recruiting |
NCT06060236 -
Dexketoprofen and Ibuprofen in Long Bone Fractures
|
Phase 4 | |
Completed |
NCT05928065 -
Ultrasound Analysis of Suspected Long Bone Fractures in the Emergency Department - Diagnostic Performance Compared to Radiography.
|
||
Recruiting |
NCT04189523 -
Does Early Administration of Ultrasound Guided Regional Anesthesia for Long Bone Fractures Effect Long Term Patient Opioid Usage
|
N/A | |
Completed |
NCT03286270 -
A mRUS Validation Study for Nail-treated Fractures of Long Bones and a TUS Exploratory Study for Nail and Plate-treated Fractures of Long Bones
|
||
Completed |
NCT01618786 -
Flooring for Injury Prevention Trial
|
N/A | |
Completed |
NCT04643912 -
Vibration as a Method of Fracture Screening in Children
|
N/A | |
Completed |
NCT02889237 -
Fracture Healing Assessed by HR-pQCT After Administration of Calcium and Vitamin D
|
N/A | |
Completed |
NCT03438123 -
Data Collection Study for the Spectrum Dynamics Multi-purpose CZT SPECT Camera
|
N/A | |
Recruiting |
NCT04766203 -
Relative Energy Deficiency in Sport Multicenter Study
|
N/A | |
Recruiting |
NCT05882435 -
Use of Augmented Intelligence for the Interpretation of Bone Standard X-rays Prescribed by the Emergency Department (IMMEDIAT Urgences)
|
N/A | |
Completed |
NCT03076138 -
Gene-activated Bone Substitute for Maxillofacial Bone Regeneration
|
N/A | |
Completed |
NCT02609074 -
Pilot Clinical Trial of CPC/rhBMP-2 Microffolds as Bone Substitute for Bone Regeneration
|
Phase 4 | |
Not yet recruiting |
NCT05751304 -
A Comparative Study Between Intrathecal Dexmedetomidine VS Ketamine With Intrathecal Bupivacaine in Orthopedic Lower Limb Surgeries.
|
N/A | |
Completed |
NCT03082417 -
The PAINFREE Initiative, a Stepped Wedge Cluster Randomized Trial
|
N/A | |
Recruiting |
NCT02448849 -
Autologous BM-MSC Transplantation in Combination With Platelet Lysate (PL) for Nonunion Treatment
|
Phase 2/Phase 3 | |
Recruiting |
NCT04528446 -
The Impact of Glomerular Disorders on Bone Quality and Strength
|
||
Recruiting |
NCT05883241 -
Sustained Acoustic Medicine (SAM) for Symptomatic Treatment of Pain Related to Bone Fracture
|
Phase 1 |