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The goal of this observational study is to evaluate the feasibility and clinical utility of radiomics to diagnose peri-lesion tumour infiltration of tumours in participants with a suspect of Bone Cancer Tumor or Soft Tissue Sarcoma (STS).
The main questions it aims to answer are:
Participants eligible for this study will get a MRI as part of their regular medical care. The only difference is that their data will be recorded and anonymously analyzed.
Enrollment
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Inclusion criteria
Exclusion criteria
simultaneous cancer or history of cancer in the last 5 years
acute or chronic serious conditions that could
contraindication to conduct a Contrast-enhanced magnetic resonance imaging (MRI) such as:
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Central trial contact
Vincenzo Lucidi, MD
Data sourced from clinicaltrials.gov
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