Ireland
--:--IST
Recruiting Observational

Spectral Cancer Tissue Recognition - I

NCT07459062 · tracked via the Priya Life Science Netherlands tracker
Sponsor
SPCTR
Phase
Observational
Started
2026-01-12
Last updated
2026-03-09

Condition(s) studied

Margin AssessmentBreast Cancer

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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥18 years * Confirmed diagnosis breast cancer for which surgical procedure is needed * Planned for breast conserving surgery Exclusion Criteria: * Person that undergoes breast amputation without confirmed cancer diagnosis

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)

FacilityCityRegionStatus
Martini Ziekenhuis Groningen Provincie Groningen Recruiting
UMC Utrecht Utrecht Utrecht Not Yet Recruiting
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 NCT07459062 on ClinicalTrials.gov ↗ ← All trials in the Netherlands