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Clinical Trial Summary

All patients will be provided with a Preprogen Pad to be worn for 4-6 hours to collect cells shed by the endometrium. After the kit is returned to the Preprogen laboratory, a brief survey will be completed. Analysis will be conducted to determine if the PadKit™ can collect a sample of endometrial cells sufficient to differentiate between normal and atypical hyperplasia/malignant cells in blinded samples provided to the laboratory for analysis.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06464107
Study type Interventional
Source Hackensack Meridian Health
Contact Diane Russomanno
Phone 7327762421
Email diane.russomanno@hmhn.org
Status Recruiting
Phase N/A
Start date May 31, 2024
Completion date May 30, 2026

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