Clinical Trials Directory

Trials / Completed

CompletedNCT04478760

Trans & Non-binary Reference Intervals While on Hormone Therapy Study

Reference Intervals for 27 Routine Chemistry and Immunoassay Tests in Transgender Adults on Stable Hormone Therapy

Status
Completed
Phase
Study type
Observational
Enrollment
250 (actual)
Sponsor
King's College Hospital NHS Trust · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

This study will find out what the reference intervals are for common blood tests in transgender people taking hormone therapy. Reference intervals help doctors interpret blood test results. They are expressed as two numbers, and most normal results fall between them. If a results fall outside of them, it may be because of a disease. Some blood tests are also affected by normal difference between people, such as age, sex or ethnicity. For these tests, different reference intervals are given for each group of people. Having accurate reference intervals benefits patients because it allows doctors to identify disease faster. Transgender people have a gender identity which does not match their sex characteristics at birth. Gender identity is the feeling of being a gender, and sex is the biological aspects of growing up male or female. Transgender people may use hormone therapy to help change their appearance to fit their gender identity. This involves taking either oestrogen or testosterone. For blood tests which are affected by sex, it is not clear what reference intervals should be used for transgender people who are on hormone therapy. This is because they have a mixture of male and female sex characteristics. Answering this question will allow doctors to identify disease in them faster. The study will take place at cliniQ, at King's College Hospital, which provides health services to transgender people. It will recruit healthy transgender people who attend the clinic for blood tests to monitor their hormone therapy. Participants will fill out a questionnaire, give a urine sample, then have their appointment as normal. Extra tests will also be performed on their blood sample. The aim is to recruit 240 participants. Participant's tests results will then be used to calculate reference intervals. The study is funded by Viapath Group LLP.

Conditions

Timeline

Start date
2021-04-13
Primary completion
2024-05-14
Completion
2024-05-14
First posted
2020-07-21
Last updated
2025-09-03

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT04478760. Inclusion in this directory is not an endorsement.