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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06305156
Other study ID # CT_BMD_1
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 13, 2024
Est. completion date March 2025

Study information

Verified date March 2024
Source University of Zurich
Contact Hatem Alkadhi, MD, MPH
Phone +41 44 255 36 62
Email hatem.alkadhi@usz.ch
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Bone mineral density is an important measurement to detect osteoporosis. The goal of this clinical trial is to compare bone mineral density measurements in CT examinations and DXA scans. The main question it aims to answer is: - How good is the measurement of bone mineral density in the new photon-counting CT in comparison to DXA - How can we optimize the CT scan for bone mineral density Participants will undergo: - Clinically indicated CT scan on day of inclusion - Study related DXA scan on a separate appointment


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date March 2025
Est. primary completion date March 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Informed Consent signed by the subject - Referral to a regular clinically indicated CT examination covering the lumbar area (e.g., Abdomen, Thorax + Abdomen, Neck + Thorax +Abdomen) - Informed written and oral consent (interpreter present in case of foreign language patients) - No contraindication to the clinically indicated CT examination Exclusion Criteria: - Patients < 18 years - Pregnant women - Vulnerable subjects - Contraindications to the clinically indicated CT scan - Multiple Myeloma - Diffuse bone metastasis - Fixateur interne in the lumbar spine - Kyphoplasty in the lumbar spine - Enterally administrated contrast agent - Obtaining informed consent is not possible - Withdrawal of consent orally or in writing - Inability to follow the procedures of the investigation, e.g., due to language problems, psychological disorders, dementia, etc. of the subject - Immobility (patients confined to a wheelchair or to bed)

Study Design


Intervention

Diagnostic Test:
Bone Mineral Density quantification
In the first visit, participants receive clinically indicated CT scan, where bone mineral density will be derived. In a second, study related visit, participants will receive a DXA scan for bone mineral quantifications.

Locations

Country Name City State
Switzerland Diagnostic and Interventional Radiology, University Hospital Zurich Zürich

Sponsors (1)

Lead Sponsor Collaborator
Hatem Alkadhi

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Bone mineral density CT Bone mineral density derived from CT Scan Immediately after CT scan of the participant.
Primary Bone mineral density Dual-energy x-ray absorptiometry (DXA) Bone mineral density derived from DXA Scan Immediately after DXA scan of the participant.
Secondary Correlation between age and bone mineral density Correlation analysis by means of linear regression and pearson correlation between age (in years) and bone mineral density 1 year
Secondary Correlation between sex and bone mineral density Correlation analysis by means of linear regression and pearson correlation between sex (male/female) and bone mineral density 1 year
Secondary Correlation between height and bone mineral density Correlation analysis by means of linear regression and pearson correlation between height (in cm) and bone mineral density 1 year
Secondary Correlation between weight and bone mineral density Correlation analysis by means of linear regression and pearson correlation between weight and bone mineral density 1 year
Secondary Correlation between body mass index (BMI) and bone mineral density Correlation analysis by means of linear regression and pearson correlation between body mass index (BMI, in kg/m^2) and bone mineral density 1 year
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