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319364

Hpv self-testing in transgender individuals
Source : Importé depuis le centre

Référence clinicaltrials.gov: NCT05883111
Transgender
Trans men
Trans women
Non-binary individuals
Source :Importé depuis le centre
HPV Infection
Recrutement fermé
Dernière modification : 2026/02/18
Type de recherche

Interventionnel


Population cible

Condition médicale (spécialité visée)

Choix aire thérapeutique

HPV Infection

Source : Importé depuis le centre

Profil des participants

Limites d'âge
minimum : 21 ans maximum : 65 ans
Sexe(s) des participants

ALL

Source : Importé depuis le centre

Critères de sélection

Critères d'inclusion

Inclusion criteria for trans men and non-binary adults with a cervix:

* Identify as transgender or non-binary
* Be between 25 - 65 years of age
* Be registered with a general practitioner
* Have an intact cervix
* Have used testosterone therapy within the last year
* Be willing, and able to understand and consent to study procedures

Inclusion Criteria for trans women and non-binary adults :

* Identify as transgender or non-binary
* Be 18 years of age or older
* Have undergone vaginoplasty by any method at least 1 year ago
* Be willing, and able to understand and consent to study procedures

Exclusion Criteria:

* Have a variation of sex characteristics (also known as a disorder of sex development)
* Have an allergy to any of the ingredients in the oral rinse (Scope)
* Be diagnosed with, or under investigation for, an inflammatory bowel disease (e.g., ulcerative colitis, Crohn's disease). This does not include irritable bowel syndrome - participants with this are eligible to enroll.
* Be a member of a vulnerable population, which includes pregnant people, fetuses, children, prisoners, or anyone unable to independently offer consent.

Source : Importé depuis le centre

Thérapie ou Intervention proposée

Cohortes
Nom Condition médicale Traitement État du recrutement
Trans men and non-binary people with a cervix Participants will have a clinician-collected cervical screening sample and then collect the following self-samples for research: Vaginal swab, Anal swab, Oral rinse, and Urine sample for the detection of HPV detection. Donnée non disponible
  • Inconnu
  • Trans women and non-binary people Participants will collect the following self-samples for research in the clinic: Vaginal swab, Anal swab, Oral rinse, and Urine sample for the detection of HPV detection. Participants will collect the following self-samples for research at home: Vaginal swab, Anal swab, and Oral rinse sample for the detection of HPV detection. Donnée non disponible
  • Inconnu
  • Trans men and non-binary people with a cervix
    État du recrutement
    unknown
    Trans women and non-binary people
    État du recrutement
    unknown
    Données à jour depuis : 18 février 2026

    Description de l'étude

    Résumé de l'étude

    Human papillomavirus (HPV) is a common virus that spreads through skin-to-skin contact. Some HPV types can cause changes in cells that lead to cancer and are known as 'high-risk' HPV (hrHPV). hrHPV is linked to cancers of the cervix (opening of the womb), throat, and anus (exit of the bowel).

    It is not known if transgender people (individuals whose gender identity does not align with their sex assigned at birth) are at increased risk of hrHPV or cancers caused by hrHPV compared to cisgender people (individuals whose gender identity does align with their birth sex). There is also little knowledge about HPV in the vagina for transgender women who have surgery to make one.

    Transgender men may be at higher risk of cervical cancer than cisgender women because they are less likely to go for screening. This can be because of physical discomfort and emotional distress during screening when a swab is taken directly from the cervix.

    The investigators seek to examine how common hrHPV is in transgender people in different parts of the body. In the study, participants will take swabs from the vagina and anus, a urine sample, and use mouthwash. Transgender men will also have an extra swab taken by a clinician as part of routine cervical screening. This is to see if the swab from the vagina is as good as the one from the cervix for finding cells that might lead to cancer. Participants will also take an online survey to measure the acceptability of self-sampling compared to clinician sampling.

    This research can inform HPV prevalence and decision-making about HPV screening among transgender people.

    Source : Importé depuis le centre

    Sites

    Centres participants

      3 centres
    • AMBROSE KING CENTRE, BARTS HEALTH NHS TRUST

      London

      UNITED KINGDOM

      Recrutement local
      État du recrutement: FERMÉ
    • CLINIQ, CALDICOTT CENTRE, KINGS COLLEGE HOSPITALS

      London

      UNITED KINGDOM

      Recrutement local
      État du recrutement: FERMÉ
    • UNIVERSITY HOSPITALS SUSSEX NHS FOUNDATION TRUST SEXUAL HEALTH SERVICE

      Brighton

      UNITED KINGDOM

      Recrutement local
      État du recrutement: FERMÉ

    Dernière modification : 18 février 2026
    Données à jour depuis : 20 fév.
    Origine des données : clinicaltrials.gov
    Référence clinicaltrials.gov: NCT05883111