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Clinical Correlation Between Self-collected and Physician-collected HPV Screening Kits

NCT05679141 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 344

Last updated 2024-04-26

No results posted yet for this study

Summary

The objective of this study is to validate the of the Evalyn®Brush via self-collection to the standard clinician-collected technique using the BD SurePath™ collection vial and Rovers CombiBrush for detection of Human Papillomavirus (HPV). This study will validate the sensitivity and specificity of the Evalyn Brush with the future goal of making this testing approach available for self-collection in the future.

Conditions

Sponsors & Collaborators

  • Switch Health Solutions Inc.

    lead INDUSTRY

Principal Investigators

  • Karam Ramotar, PHD · Bio-Test Laboratory

Eligibility

Min Age
21 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-02-01
Primary Completion
2024-03-19
Completion
2024-03-19

Countries

  • Canada

Study Locations

More Related Trials

Entities

Diseases

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 NCT05679141 on ClinicalTrials.gov