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Study to Evaluate the Effectiveness of the Personal Pap Smear Device™ for Collection of Cervical Cells

Cervical Cancer Screening Clinical Trial

Official title:
A Phase III Cross-Over Comparative Study to Evaluate the Effectiveness of the Rover Cervex-Brush Device vs. the Personal Pap Smear Device™ for Collection of Cervical Cells for Detecting Cervical Dysplasia or Neoplasia

Clinical Trial Summary

This purpose of this research study is to determine the effectiveness of the Personal Pap Smear TM Device to collect adequate cervical cell samples for cytology examination when compared with the Rover Cervex-Brush (Cervix-Examination Brush).

Clinical Trial Description

To determine the effectiveness of the Personal Pap Smear TM Device to collect adequate (as defined by Bethesda Guidelines 2014) cervical cell samples for cytology examination as compared with the Rover Cervex-Brush (Cervix-Examination Brush). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06229275
Study type Interventional
Source Morehouse School of Medicine
Contact Regina K Leonis, MD
Phone 4047565713
Email rleonis@msm.edu
Status Not yet recruiting
Phase Phase 3
Start date February 2, 2024
Completion date March 30, 2026
View Details
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