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NCT03222817 · ClinicalTrials.gov registry record · NA

HPV Self-Sampling for Cervical Cancer Screening Among Transgender Men and Transmasculine Individuals

A NA study, sponsored by University of Miami.

Completed
Registry status
NA
Development phase
10
Enrollment target

NCT03222817: Completed NA study, sponsored by University of Miami.

NCT03222817 is a NA study that has completed, run by University of Miami. The registered enrollment target is 10 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03222817, a NA study, has completed, sponsored by University of Miami.

COMPLETED
Registry status
NA
Development phase
10 participants
Enrollment target

Study Summary

The proposed study will examine the implementation of a Human Papillomavirus (HPV) self-sampling intervention for unscreened and under-screened transgender men and transmasculine individuals living in South Florida. The study will enroll participants to receive this cervical cancer screening intervention in community venues. The purpose of this study is to pilot the self-sampler for feasibility and acceptability within this underserved population.

Primary Outcome

This questionnaire, designed with substantial input from community partners, will gauge how acceptable the participants find HPV self-sampling through both closed and open-ended questions regarding ease of use, preference of self-sampler vs. physician-collected Pap smear, as well as open-ended inquiries regarding the self-sampling process.

Interventions

  • BEHAVIORAL HPV self-sampling

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2018-05-12
Est. Completion 2018-10-17
Phase NA
University of Miami

721 total trials

What the finished NCT03222817 record still lists

NCT03222817 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 1 intervention - of which HPV self-sampling is the first listed.

NCT03222817 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03222817 about?

NCT03222817 is a clinical study titled "HPV Self-Sampling for Cervical Cancer Screening Among Transgender Men and Transmasculine Individuals". The proposed study will examine the implementation of a Human Papillomavirus (HPV) self-sampling intervention for unscreened and under-screened transgender men and transmasculine individuals living in South Florida. The study will enroll participants to receive this cervical cancer screening interve...

What is the current status of trial NCT03222817?

This trial is currently completed. It is a NA study. The enrollment target is 10 participants. The study started on 2018-05-12. Estimated completion is 2018-10-17.

What interventions are being tested in trial NCT03222817?

The interventions under investigation include: HPV self-sampling (BEHAVIORAL).

Who is sponsoring clinical trial NCT03222817?

This trial is sponsored by University of Miami, which has 721 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03222817's enrollment target sits among peer trials

10 1927th of 2000 higher than 26 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 NCT03222817, the US trial registry maintained by the National Library of Medicine. NCT03222817 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.