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NCT06305156Completed

Protocol Optimization in CT for the Quantification of BMD

Protocol-optimization in Computed Tomography for the Quantification of Bone Mineral Density (BMD)

Source: ClinicalTrials.gov · Last updated 13 Jan 2026

Brief summary (registry, in English)

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

Status (registry)
Completed
Study type
Interventional
Enrollment
167 (actual)
First submitted
22 Feb 2024
Start date
13 Mar 2024
Primary completion date
19 Dec 2025
Lead sponsor
Hatem Alkadhi
Diseases
Osteoporosis
NCT number
NCT06305156

What you commit to

  • Study type: Interventional
  • Participants enrolled: 167
  • From 13 Mar 2024 to the primary completion date, 19 Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Inability to follow the procedures of the investigation, e.g., due to language problems, psychological disorders, dementia, etc. of the subject

Age

  • Patients \< 18 years

Other

  • 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
  • Immobility (patients confined to a wheelchair or to bed)

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Diagnostic and Interventional Radiology, University Hospital Zurich
Coordinator of this site? Confirm its status
ZurichSwitzerlandUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.