Clinical studies
Studies are essential to clinically validate our innovations and ensure they meet the highest standards of care. They allow us to evaluate the effectiveness and reliability of our devices, optimize our solutions using precise data, demonstrate the advantages of our technologies compared to traditional methods, and assess their medico-economic benefits.
Prospective, multicenter – French study
Bladder cancer
VitaDX International
Phase 1: Develop the most effective image processing algorithm, capable of distinguishing cancerous from non-cancerous urothelial bladder cells. Phase 2: Evaluate the diagnostic performance (sensitivity and specificity) of urine analysis using the VisioCyt® Bladder test."
No reuse in progress
Prospective, multicenter – European study
Bladder cancer
VitaDX International
Demonstration of the benefit of the VisioCyt® Bladder solution through comparison with conventional urine cytology for the detection of recurrences in patients under follow-up for high- and very high-risk non–muscle-invasive bladder tumors.
No reuse in progress
Bladder Cancer
Institut Paoli-Calmettes et VitaDX International
Measure the negative predictive value (NPV) and sensitivity of VisioCyt® Bladder in real-world clinical settings.
No reuse in progress
Prospective, multicenter French study
Bladder cancer
Association Française d'Urologie
To deepen knowledge of bladder tumors and to evaluate, in real-world settings, biomarkers that could ultimately reduce unnecessary cystoscopies and improve patient comfort.
No reuse in progress
Bladder cancer
Institut de Cancérologie de Lorraine
To evaluate the VisioCyt® urinary cytology technique combined with FGFR3 mutation analysis in urine for the diagnosis of bladder cancer, compared with the VisioCyt® urinary cytology technique alone.
No reuse in progress
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Your participation plays a key role in the development of innovative technologies that improve cancer care.
Data protection
Among the projects listed above, some studies may involve the reuse of data in a new project. If this occurs, you will be informed through the note ‘reuse of data collected from the study’ in the corresponding study sheet.
With your consent, your data may be reused and shared for other health research projects. You will have the option to object to this reuse at any time by contacting VitaDX’s Data Protection Officer.
You have the right to access your data, correct it, and object to its processing in accordance with current regulations.
You also have the following rights:
The right to request a restriction on the processing of your data;
The right to be forgotten and to have your data digitally erased;
The right to set general instructions regarding the retention, deletion, and sharing of your data after your death.
If, after contacting us, you believe your rights are not being respected, you may file a complaint with the CNIL.
In the context of a study, if the processing of your data is based on your consent, you also have the right to data portability.
To exercise your rights, you can send your requests by email to VitaDX’s Data Protection Officer at the following address: [email protected].
