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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04265885
Other study ID # 2020PI033
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date October 2020
Est. completion date September 2021

Study information

Verified date July 2020
Source Central Hospital, Nancy, France
Contact Eva Feigerlova, MD, PhD
Phone +33(0)83155032
Email e.feigerlova@chru-nancy.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Persons with gender dysphoria present the difficulties of access to health care. Little time is devoted to education of health professionals about the care of transgender persons. According to the proposal of the French Ministry of Social Affairs and Health there is a need to increase knowledge in this area and to improve the care of transgender people including prevention and screening.

Similarly, little is known about social and medical needs of the transgender population.

This project proposes to illustrate gender dysphoria through testimonies of transgender people with the aim to increase the investigator's understanding aout the needs and the desires of this population and to describe the process of medical and social transition.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 10
Est. completion date September 2021
Est. primary completion date June 2021
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Person affiliated to a social security system

- Person having received complete information on the organisation of the research and having signed the informed consent

- Person having carried out a prior clinical examination adapted to the research

- Age> 18 years

- Diagnosis of gender incongruence (dysphoria) according to the international classification of diseases, revision 11

Exclusion Criteria:

- Severe, uncontrolled psychiatric or somatic illness

- Substance and alcohol addiction

- Pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Other:
collection of testimonies from transgender people
guided interview

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Central Hospital, Nancy, France University of Lorraine

Outcome

Type Measure Description Time frame Safety issue
Primary Illustrate the real-life experiences of transgender people 4 months
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