Spectral Cancer Tissue Recognition - I
Condition(s) studied
Study summary
This analytical performance study aims to validate the SPCTRone system for use in breast conserving surgery of breast cancer patients. By collecting spectral biomarkers and correlating these with the golden standard of histopathological assessment by a pathologist, we aim to train and optimize an AI model that is able to achieve the following outcomes with classifying tissues:
* Sensitivity (percentage of classified positive margins of actual positive margins): ≥ 96% CI 95.5-97.5%
* Specificity (percentage of classified free margins of actual free margins): 96% CI 95.5-97.5%
* Accuracy (total correctly classified margins): ≥ 96% CI 95.5-97.5%
* Negative predictive value (amount of true negative - free margins - among the classified negative margins): ≥ 95% CI 94.5-96.5%
Eligibility
Primary outcome measure(s)
- Diagnostic performance of SPCTRone system to assess margin status of breast cancer specimens — Through study completion, an average of 6 months
Diagnostic performance indicators are: Sensitivity, Specificity, Negative Predictive Value, and Accuracy.
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Martini Ziekenhuis | Groningen | Provincie Groningen | Recruiting |
| UMC Utrecht | Utrecht | Utrecht | Not Yet Recruiting |
Other trials for the same condition
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 NCT07459062 on ClinicalTrials.gov ↗ ← All trials in the Netherlands