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Comparison of Self-collection Using Dry Compared to Wet Swabs for HPV Detection

NCT06213051 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 1306

Last updated 2024-07-29

No results posted yet for this study

Summary

This study will compare the performance of self-collected vaginal swabs, transported without liquid media (dry swabs) and self-collected vaginal swabs, transported in liquid media (wet swabs) for detection of hrHPV DNA LBC as the reference standard.

Conditions

  • Human Papillomavirus Infection

Interventions

DEVICE

• COPAN Self-collection FLOQSwabs® (COPAN, Italy)

COPAN swabs evaluated on Roche COBAS and Cepheid Xpert PCRs

Sponsors & Collaborators

  • Kenya Medical Research Institute

    collaborator OTHER

  • Frere Hospital, East London, South Africa

    collaborator UNKNOWN

  • Bangabandhu Sheikh Mujib Medical University, Bangladesh

    collaborator UNKNOWN

  • Foundation for Innovative New Diagnostics, Switzerland

    lead OTHER

Principal Investigators

  • Angela Muriuki · Foundation for Innovative New Diagnostics (FIND)

Eligibility

Min Age
30 Years
Max Age
80 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-07-25
Primary Completion
2024-09-30
Completion
2024-09-30

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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 NCT06213051 on ClinicalTrials.gov