Retrospective Study of the Cohort of Transgender Patients Who Began Medical Support Before the Age of 18
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Endocrinology. Basic parameters: 8 years — 17 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Retrospective Single-center Study of the Cohort of Transgender Patients Who Began Medical Support Before the Age of 18 at the Strasbourg University Hospital
Overview
Gender incongruence is characterized by a marked and persistent incongruity between the gender with which a person identifies and their assigned sex. Behaviors and preferences that vary by sex do not, in and of themselves, justify the assignment of diagnoses in this group.
Primary outcome measures
- Retrospective descriptive study of the population of transgender minors receiving medical support at the Strasbourg University Hospital [Time frame: Up to 1 year]
Eligibility criteria
Inclusion criteria
- Minor patient (≥18 years old)
- First-time patient for transgender issues at the Strasbourg University Hospital in child psychiatry and/or pediatric endocrinology (in at least one of the two departments)
- Patient (and/or their legal representative) who has not expressed opposition to the reuse of their data for scientific research purposes.
Exclusion criteria
- Patient (and/or their representative) who has expressed opposition to the reuse of their data for scientific research purposes.
- Patient aged over 18 at the first consultation
- Patient with insufficient data
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Case-only
Study locations
France · 1 center
- Service de pédiatrie 1 - CHU de Strasbourg - France — Strasbourg
Identifiers
NCT: NCT07163832 · 9688