Instrument Precision Study for Validation of Philips Dx

Completed

Conditions studied: Pathology

In brief

The objective of this study is to evaluate precision of the Philips Dx system.

Key facts

Study ID

NCT02699970

Run by

Philips Digital & Computational Pathology

People needed

399

Starts

2016-02-01

Expected to finish

2016-10-01

Last updated by the study team

2019-11-01

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Left-over specimens from subjects who already received their diagnosis and have received their treatment in accordance with the standard of care
• H\&E glass coverslipped slides with human tissue obtained via surgical pathology
• Selected slides fulfill the quality checks according to the Instructions for Use (lfU)
• Selected slides must be between 1-5 years since accessioning
• Selected slides and FOVs must contain a study feature that is: In it's natural environment (on slide and FOV); Readily observable (on slide and FOV); Not equivocal (on slide and FOV).

You may not qualify if…

• Selected slides contain indelible markings
• Selected slides contain damaged tissue
• More than one slide was selected for a patient (only one slide may be enrolled per patient).

Where it is running

• MGH — Boston, Massachusetts, United States

Full record on ClinicalTrials.gov

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