Histolog Comparison to Standard Histology

NCT04857229 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 101

Last updated 2023-02-14

No results posted yet for this study

Summary

This is a clinical device trial to assess the accuracy of margin assessment for a confocal scanning device (Histolog Scanner) at assessing the margins of breast tissue following wide local excision surgery.

Conditions

Interventions

DEVICE

Histolog Scanner

Confocal Microscope

Sponsors & Collaborators

  • SamanTree Medical SA

    collaborator INDUSTRY
  • Imperial College London

    lead OTHER

Principal Investigators

  • Daniel R Leff, MBBS FRCS (Gen Surg) MS PhD · Imperial College London

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-06-04
Primary Completion
2023-12-31
Completion
2023-12-31

Countries

  • United Kingdom

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04857229 on ClinicalTrials.gov