Lung Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Adults aged 18 or older.
- People who do not object to taking part in the study (and for those involved in the biological collection part of the study, a signed written consent form is required).
- People who have secondary bone tumours (cancer that has spread to the bones) originating from breast cancer, non-small cell lung cancer, kidney cancer, bladder cancer, thyroid cancer, or myeloma.
- People who have had, or will have as part of their usual care, a CT scan focused on the affected area taken within 30 days before or 20 days after joining the study.
- People whose affected bone is located in the upper part of the thigh bone (upper third of the femur) and/or in one or more vertebrae (bones of the spine). More than one location in the same person may be included, as long as each location meets the criteria.
- People whose affected area in the bone is either widespread through the bone or measures more than 15 mm in size.
- People who have been receiving certain bone-strengthening medications (such as clodronate, denosumab, zoledronic acid, or pamidronate) for 3 months or less are eligible.
- People who have previously received cancer treatments such as chemotherapy, targeted therapy, or immunotherapy are eligible.
Who may not be able to join:
- People who have already received treatment directed specifically at the target bone area, whether that was radiotherapy, surgery, or procedures such as cementoplasty, cryotherapy, or radiofrequency treatment.
- People whose target bone has already fractured.
- People being considered for the thigh bone (femur) target location who have a hip replacement on either side (the affected side or the other side).
- People who are under legal guardianship or trusteeship.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Cyrille CONFAVREUX, PR, Service de Rhumatologie
Phone: 4.78.86.12.31
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Measurement of mechanical strength of tumor proximal femur or tumor vertebrae obtained by numerical simulation using the finite element analysis (FEA) method.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 15 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.