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Instrument Precision Study for Validation of PIPS 5.1

NCT04879056 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 399

Last updated 2022-05-19

No results posted yet for this study

Summary

This study is designed to evaluate the instrument precision of the device for its proposed intended use in sub-studies: intra-system and inter-system. The precision within a system will be evaluated on three systems by three pathologists at one site. Specific features will be selected on glass slides, which will then be scanned. On the whole slide images field of views will be created including the features. In the reading phase three pathologists will read the field of views and record which features they observe.

Conditions

  • Pathology

Interventions

DIAGNOSTIC_TEST

PIPS 5.1

Description: Scanning glass slides on PIPS 5.1. This intervention will be applied in the arm of intra-system and the arm of inter-system.

Sponsors & Collaborators

  • Philips Digital & Computational Pathology

    lead INDUSTRY

Principal Investigators

  • Mischa Nelis, MsC · Philips Digital & Computational Pathology

Eligibility

Min Age
1 Year
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-05-20
Primary Completion
2022-08-20
Completion
2022-09-20

Countries

  • United States

Study Locations

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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 NCT04879056 on ClinicalTrials.gov