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Recruiting NCT06958991

NCT06958991 Confocal Histolog Scanner in Routine Breast-Conserving Surgery (CHiB)

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Clinical Trial Summary
NCT ID NCT06958991
Status Recruiting
Phase
Sponsor University of Fribourg
Condition Breast Cancer Invasive
Study Type INTERVENTIONAL
Enrollment 100 participants
Start Date 2025-06-01
Primary Completion 2026-07-30

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Histolog Scanner

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 100 participants in total. It began in 2025-06-01 with a primary completion date of 2026-07-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The clinical performance study is collecting data from the use of a CE mark product used within the scope of its intended purpose to intraoperatively visualize tissue specimen. The subjects are not submitted to invasive and burdensome procedures compared to the standard of care surgical practices and regular use of the CE mark product.

Eligibility Criteria

Inclusion Criteria: * Adult female Subject ≥18 years old. * Subject scheduled for breast conserving surgery of invasive and/or in-situ ductal and lobular carcinoma. * Subject is able to read, understand and sign the informed consent. Exclusion Criteria: * Subject with planned mastectomy * Subject does not speak French- Subject with planned tumor-adapted breast reduction * Subject is pregnant/ lactating. Subjects pregnant/lactating are excluded because such subjects are presenting additional risks during the surgery and they are also rare. * Participation in any other clinical study that would affect data acquisition.

Frequently Asked Questions

Who can join the NCT06958991 clinical trial?

This trial is open to female participants only, aged 18 Years or older, studying Breast Cancer Invasive. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06958991 currently recruiting?

Yes, NCT06958991 is actively recruiting participants. Visit ClinicalTrials.gov or contact University of Fribourg to inquire about joining.

Where is the NCT06958991 trial being conducted?

This trial is being conducted at Villars-sûr-glâne, Switzerland.

Who is sponsoring the NCT06958991 clinical trial?

NCT06958991 is sponsored by University of Fribourg. The trial plans to enroll 100 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology