Bone Lesion

4

Review clinical trials related to Bone Lesion. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Contribution of MUltiparametric Analysis in Bone Scintigraphy for the Characterisation of Solitary Bone Lesions

The hypothesis of the study is that non-invasive Single photon emission computed tomography (SPECT-CT) bone scintigraphy makes it possible to better characterize solitary bone lesions, in particular the exclusion of their malignancy in order to avoid unnecessary biopsy and possible complications for the patient.

Participants needed: 68
Trial details
Age: 18-90Biological sex: AllType: InterventionalSponsor: Central Hospital, Nancy, FranceUpdated: Jun 25, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years old. [+3]

Pregnant woman or woman of childbearing age and without contraceptive means or n... [+4]

Status: Recruiting

Assessing AI-Supported Fracture Detection in Emergency Care Units

Brief Summary The purpose of this study is to determine if artificial intelligence (AI) can assist doctors in detecting broken bones, effusions, dislocations and bone lesions more quickly and accurately in an emergency room setting. The study will also evaluate whether AI can save time and reduce costs in healthcare. The main questions to be addressed are: * Does AI improve the accuracy of detecting broken bones/dislocations/effusions/bone lesions? * Can AI expedite the process of diagnosing broken bones/dislocations/effusions/bone lesions? * Does AI reduce healthcare costs by enhancing efficiency? To investigate these questions, two groups of patients will be compared. One group will follow the traditional diagnostic approach, while the other group will utilize AI to assist in diagnosing X-rays. Participants in the study will: Undergo standard X-ray imaging of injured arms or legs, as part of routine care. Have X-rays reviewed by doctors with or without AI support, depending on the assigned group. The study will include patients of all ages presenting to the emergency room with an isolated injury or joint complaints. No additional tests or treatments beyond standard care will be involved.

Participants needed: 4,800
Trial details
Biological sex: AllType: InterventionalSponsor: Salzburger LandesklinikenUpdated: Jan 22, 2026Locations: 3
Eligibility criteria

Presenting to the emergency department with an isolated injury or joint complain... [+1]

Patients with injuries or complaints involving multiple body regions [+4]

Status: Not yet recruiting

A Study on the Diagnostic Value of 99mTc-FAPI Quantitative SPECT/CT Imaging in Adult Solitary Bone Lesions

Using the novel FAPI probe 99mTc-HYNIC-FAPI-04 and quantitative SPECT/CT imaging technology, this study investigates the diagnostic efficacy of 99mTc-HYNIC-FAPI-04 quantitative SPECT/CT in patients with common solitary bone lesions in adults, and compares its diagnostic performance with conventional CT, MRI, and 99mTc-MDP bone scintigraphy. Follow-up pathological results of patients post-surgery were analysed to assess the accuracy of 99mTc-HYNIC-FAPI-04 diagnostic outcomes, and its diagnostic value and significance were evaluated.

Participants needed: 50
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Xijing HospitalUpdated: Aug 11, 2025
Eligibility criteria

Benign solitary bone lesions in adults (fibrous cortical defects, fibrous hyperp...

Severe liver and kidney dysfunction; Pregnant women and breastfeeding patients;...

Status: Recruiting

Efficacy of Bioceramic Materials for Bone Defects Repair

The purpose of this study is to demonstrate the effect of bioceramic implants on the repair of human bone defects, and to explore the application of bioceramic materials in bone defects, bone implantation, and bone fusion. The surface microstructure of β-tricalcium phosphate bioceramic implants can be effectively controlled to guide the regeneration of bones, promote the restoration of bones, accelerate the speed of recovery, and improve bone quality, which is of great clinical and social significance.

Participants needed: 10
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Nanjing First Hospital, Nanjing Medical UniversityUpdated: Mar 12, 2024Locations: 1
Eligibility criteria

Patients who voluntarily take the test and sign the informed consent form; [+2]

Patients who refuse to sign the informed consent form to participate in the tria... [+5]