Transmasculine Quality of Life and Sexual Function at Pre and Post Gender-affirming Hormonal Therapy

This study was designed as a single-center, prospective trial at King Chulalongkorn Memorial Hospital, Bangkok, Thailand between September 2022 to February 2024.

All hormone-naïve TM aged above 18 years who planned to start testosterone at Gender Health Clinic, King Chulalongkorn Memorial Hospital, Thailand were approached. All the enrolled participants will be received information about the study and written consent was obtained from all participants before the start of the study. The demographic data were recorded. Blood samples of serum estradiol, total testosterone and other laboratory investigations will be assessed including complete blood count, liver function test and lipid profiles. Then, the WHOQOLBREFTHAI questionnaire and Thai version of Female sexual function index questionnaire (FSFI) will be assessed before testosterone administration. All TM participants will be received 250 mg of testosterone enanthate intramuscularly every 4 weeks for 12 weeks. After 12 weeks of treatment, another laboratory investigations and 2 questionnaires, (WHOQOLBREFTHAI and FSFI) will be assessed again.

Inclusion criteria

• compatible with Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5)
• had never used testosterone therapy before the enrollment

Exclusion criteria

• history of abnormal hormone functions
• ongoing treatment or current use of medications that affect hormone functions
• diagnosis of psychiatric illnesses beyond gender dysphoria by a psychiatrist
• prescription of psychiatric or neurological medications within the past 3 months up to the present study participation
• presence of chronic illnesses or severe age-related conditions, such as chronic kidney disease, chronic liver disease, or any type of cancer