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Clinical Trials in France / NCT06439784
Starting soon Not applicable

Contribution of the VERITON-CT Camera in Prostate Bone Radiostereotaxy

NCT06439784 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2026-09-15
Last updated
2026-07-24

Condition(s) studied

Prostatic Cancer

Investigational drug(s) / intervention(s)

whole body SPECT/CT

whole body SPECT/CT: Patient will unergo a whole body SPECT/CT in treatment position

Study summary

Stereotactic radiotherapy enables bone metastases to be treated with highly precise irradiation beams, enabling small targets to be irradiated. Planning requires the use of cross-sectional imaging such as computed tomography (CT) or magnetic resonance imaging (MRI). Bone scintigraphy with Tc99m-labelled biphosphonates (T1/2=6h) is indicated in the extension assessment of prostate cancers. Thanks to the advent of single-photon emission computed tomography (SPECT) based on CZT detectors; whole-body SPECT is now compatible with clinical constraints. We propose to study the value of using whole-body SPECT for planning stereotactic radiotherapy of metastatic prostate cancer. This is a prospective, single-center, non-randomized study involving 30 patients. Patients will benefit from routine examinations (CT scan, MRI) including a bone SPECT/CT in treatment position performed on the VERITON-CT (Spectrum Dynamics, Haifa, Israel). Planning based on whole-body SPECT images will be carried out remotely from the patient's point of care. The examination will be interpreted by the nuclear physician, and planning will be based on the dosimetric CT scanner, as in standard management. Virtual replanning will be carried out at distance from treatment, incorporating SPECT imaging. Treatment plans with and without SPECT will be compared quantitatively and qualitatively. The feasibility of SPECT imaging in the treatment position will be assessed, enabling lesion location imaging and dosimetric scanning to be performed in a single examination. All therapeutic management and clinical follow-up will be carried out as part of routine care.

Eligibility

Sex
MALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥ 18 years, * Good general health WHO ≤ 1 * Informed and signed consent prior to any specific study procedure. * Patient affiliated to the social security system * Bone metastases from prostate cancer * Indication for bone stereotactic radiotherapy Exclusion Criteria: * Presence of active cancer in the previous three years * Protected adults (under guardianship or curatorship) * Unable to undergo medical monitoring for geographical, social or psychological reasons * Unable to decubitus (orthopnea, etc.), * Hypersensitivity to HDP or to one of the excipients of the radiopharmaceutical. * History of radiotherapy of the volume to be treated by stereotaxy.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Centre Henri Becquerel Rouen France

More Centre Henri Becquerel trials in France

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06439784 on ClinicalTrials.gov ↗ ← All trials in France