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NCT05600283 · ClinicalTrials.gov registry record · NA

Patient Self-sampling of HPV to Screen for Cervical Cancer

A NA study, sponsored by Mayo Clinic.

Completed
Registry status
NA
Development phase
222
Enrollment target

NCT05600283: Completed NA study, sponsored by Mayo Clinic.

NCT05600283 is a NA study that has completed, run by Mayo Clinic. The registered enrollment target is 222 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (84% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT05600283, a NA study, has completed, sponsored by Mayo Clinic.

COMPLETED
Registry status
NA
Development phase
222 participants
Enrollment target

Study Summary

The purpose of this study is to validate a patient self-sampling vaginal collection kit and laboratory testing for the detection of HPV (human papillomavirus) infection. Researchers will compare the laboratory results of self-collected vaginal swab samples to usual healthcare provider-collected cervical swab samples to determine the laboratory HPV testing accuracy of the self-collection swab.

Primary Outcome

Patient-collected vaginal swab HPV results compared with gold standard of clinician-collected cervical swab) to accurately detect HPV infection

Interventions

  • DIAGNOSTIC_TEST Swab kit (COBAS HPV 4800 Assay -Evalyn brush)
  • DIAGNOSTIC_TEST Clinician-collection of cervical sample for HPV testing

Trial Details

FieldValue
Enrollment Target 222 participants
Start Date 2022-11-16
Est. Completion 2024-06-04
Phase NA
Mayo Clinic

2,844 total trials

What the finished NCT05600283 record still lists

NCT05600283 is an interventional study that assigns participants to a tested intervention. The registered 222 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (84% lower).

The record links to 0 conditions, and to 2 interventions - of which Swab kit (COBAS HPV 4800 Assay -Evalyn brush) is the first listed.

NCT05600283 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05600283 about?

NCT05600283 is a clinical study titled "Patient Self-sampling of HPV to Screen for Cervical Cancer". The purpose of this study is to validate a patient self-sampling vaginal collection kit and laboratory testing for the detection of HPV (human papillomavirus) infection. Researchers will compare the laboratory results of self-collected vaginal swab samples to usual healthcare provider-collected cerv...

What is the current status of trial NCT05600283?

This trial is currently completed. It is a NA study. The enrollment target is 222 participants. The study started on 2022-11-16. Estimated completion is 2024-06-04.

What interventions are being tested in trial NCT05600283?

The interventions under investigation include: Swab kit (COBAS HPV 4800 Assay -Evalyn brush) (DIAGNOSTIC_TEST), Clinician-collection of cervical sample for HPV testing (DIAGNOSTIC_TEST).

Who is sponsoring clinical trial NCT05600283?

This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05600283's enrollment target sits among peer trials

222 481st of 2000 higher than 1,520 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05600283, the US trial registry maintained by the National Library of Medicine. NCT05600283 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.