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NCT06110442Completed

Opportunistic Fragility Fracture Risk Estimates From Radiographs

Source: ClinicalTrials.gov · Last updated 20 Jan 2025

Brief summary (registry, in English)

The proposed study will predict a patients' risk of having osteoporosis by using a combination of the IBEX BH (Bone Health) software outputs and other clinical risk factors such as age, gender, medical history and lifestyle. A comparison will be made between the IBEX BH prediction and the one calculated in current clinical practice using a tool called FRAX (Fracture Risk Assessment Tool) which combines clinical risk factors with results from a Dual Energy X-ray Absorptiometry (DXA) assessment. The study involves conducting these assessments on several new anatomies including Knee, Ankle and Pelvis, to extend the market reach and clinical utility of IBEX BH. The expected outcome of the study is that the IBEX BH will offer better decision support to clinicians in terms of referral on for a DXA scan or osteoporosis investigations than available today.

Status (registry)
Completed
Study type
Observational
Enrollment
497 (actual)
First submitted
20 Sept 2023
Start date
1 Jul 2023
Primary completion date
31 Dec 2024
Lead sponsor
University of Exeter
Diseases
Osteoporosis
NCT number
NCT06110442

What you commit to

  • Study type: Observational
  • Participants enrolled: 497
  • From 1 Jul 2023 to the primary completion date, 31 Dec 2024
  • 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

  • Women who are pregnant or are breastfeeding.
  • Participants who have sustained fractures in both hips.
  • Unwilling or unable to provide informed consent.
    • For the collection of healthy-normal data in the study.
  • Women who are pregnant or are breastfeeding.
  • Participants who have sustained fractures in both hips.
  • Unwilling or unable to provide informed consent.

Who the study is looking for

  • Male or female
  • 50 years of age or over
  • Male or female
  • 20-30 years of age

Criteria the registry did not label

  • For the collection of test data in the study.

Age in the registry: 20 years to 120 years · Sex: All · Accepts 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
University Of Exeter
Coordinator of this site? Confirm its status
ExeterUnited KingdomUnknown status

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