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Effect of Dose Fractionation of Testosterone Cypionate on Transgender Men with Erythrocytosis

U

University of Sao Paulo

Status

Completed

Conditions

Transsexualism
Testosterone
Hematologic Diseases

Treatments

Drug: Testosterone Cypionate 100 MG/ML

Study type

Interventional

Funder types

Other

Identifiers

NCT05487794
DGO-777

Details and patient eligibility

About

A transgender man is someone with a male identity who were born with a vulva and vagina. The acquisition of masculine characters can come from surgery or from the use of testosterone. Despite the benefit of using this hormone in relation to hair development, muscle mass gain and changes in voice timbre, its use can cause an increase in the hematocrit (Ht) level. When erythrocytosis occurs (Ht ≥ 50%), the currently proposed conduct is the suspension of cross-hormonization for 3 months, which has negative effects on the affirmation process. This project aims to assess whether reducing the dose of testosterone cypionate by half (100mg/15d) can mitigate the negative outcomes caused by the suspension with the benefit of reducing the hematocrit level in trans patients who developed erythrocytosis using testosterone. This is a pilot study that will compare the intervention (testosterone cypionate 100 mg, fortnightly) to the suspension of the drug, both for 3 months, with the main outcome being the hematocrit level. Hormonal and biochemical levels and the Hospital Anxiety and Depression scale (HAD) will also be evaluated in patients treated at the Gender Incongruence Outpatient Clinic of the Hospital das Clínicas of the Faculty of Medicine of Ribeirão Preto.

Enrollment

46 patients

Sex

Female

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • TM aged between 18 and 40 years in threatmeant with Testosterone Cypionate 200mg/2mL with a diagnosis of erythrocytosis (Ht⩾50%).

Exclusion criteria

  • TM with polycythemia vera or secondary to other pathologies (chronic kidney disease, severe lung disease, chronic myeloid leukemia, lymphoma, liver diseases and Cushing's syndrome);
  • TM in use of hormonal contraceptives or copper IUDs;
  • TM with psychiatric conditions such as severe psychotic disorders, severe personality disorders
  • Patients with Ht > 54.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

46 participants in 2 patient groups

Group 1 (T100)
Experimental group
Treatment:
Drug: Testosterone Cypionate 100 MG/ML
Group 1 (T0)
No Intervention group

Trial contacts and locations

1

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Central trial contact

SERGIO HENRIQUE PIRES OKANO, MSC

Data sourced from clinicaltrials.gov

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