CClinicalTrials.gg
Active, not recruitingNCT05924217GYDECATUpdated Nov 17, 2025

Gynecology Beyond Gender: Cervical Cancer Screening in Transgender Men in France

An observational study in Cervical Cancer, Transgender Persons and Health Services for Transgender Persons, sponsored by Centre Hospitalier Universitaire de Nīmes. Active, not recruiting at 1 site in France. Open to female participants aged 25 Years to 65 Years. Per ClinicalTrials.gov, last updated 2025-11-17.

Sponsored by Centre Hospitalier Universitaire de Nīmes · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
300
Ages
25 Years to 65 Years
Sex
Female
01

Study summary

In France, cervical cancer screening is the subject of a national screening programme organized for all asymptomatic individuals aged 25 to 65 years with a cervix. The latter contributes greatly to the prevention and early treatment of this disease, whose public health challenge is recognized worldwide.

One of the objectives of this programme is to reduce inequalities in access. Transgender men, i.e. individuals assigned to the female gender at birth but identifying with the male gender, are concerned by this screening as long as they still have a cervix, according to the same modalities as for cisgender women.

However, they are often excluded from health care, including organized screening programs. Gender change in civil status is one of the obstacles.

The provision of gynaecological care is sometimes inadequate. The lack of knowledge of health professionals and the problems of discrimination that transgender people may face reduce the chances of having equitable access.

This survey aims to explore the perception that transgender men have of cervical cancer screening and to identify the challenges they face, the obstacles and the levers to access this prevention program.

02

Conditions studied

  • Cervical Cancer
  • Transgender Persons
  • Health Services for Transgender Persons
03

In context

Uterine Cervical Neoplasms

1,881 studies on the registry are indexed under Uterine Cervical Neoplasms; 567 are open to participants now.

This study's planned enrollment of 300 is above the median of 220 across 419 observational studies indexed under Uterine Cervical Neoplasms.

Browse Uterine Cervical Neoplasms studies →

Lead sponsor

Centre Hospitalier Universitaire de Nīmes is the lead sponsor of 587 studies on the registry; 96 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
25 Years to 65 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Transgender men, i.e. individuals assigned the female gender at birth but identifying with the male gender, who retained the cervix

Inclusion criteria

  • transgender male (assigned female at birth but identifying as male)
  • aged 25 to 65 years
  • Having retained her cervix
  • Having had sex before.

Exclusion criteria

Exclusion Criteria:

  • Under 25 and over 65
  • Not having retained his cervix
  • History of cancerous lesion of the cervix
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
300 participants (estimated)
Patient registry
No

Interventions

  • OtherSurvey questionnaire

    This survey aims to explore the perception that transgender men have of cervical cancer screening and to identify the challenges they face, the obstacles and the levers to access this prevention program.

06

What researchers measure

Primary outcomes

  1. prevalence of transgender men who have ever been screened for cervical cancer in their lifetime

    answer yes to the question "Have you ever been screened for cervical cancer in your lifetime?"

    Time frame: At study entry, basline (no follow-up)

Secondary outcomes

  1. prevalence of transgender men who feel concerned about cervical cancer screening

    answer yes to the question "Do you feel personally involved in cervical cancer screening?"

    Time frame: At study entry, basline (no follow-up)

07

Study locations

1 site
  • CHU de Nîmes
    Nîmes, 30900, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 17, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05924217
Lead sponsor
Centre Hospitalier Universitaire de Nīmes
Responsible party
Sponsor
First posted
Jun 29, 2023
Start date
Jan 2, 2024
Primary completion
Jan 1, 2025
Completion
Jun 30, 2026 (estimated)
Last update
Nov 17, 2025

Study contacts

ingrid JULIER
principal investigator · Centre Hospitalier Universitaire de Nīmes

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Nov 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion