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

Last updated: March 24, 2025
Sponsor: University of Sao Paulo
Overall Status: Completed

Phase

N/A

Condition

Hematological Disorders

Red Blood Cell Disorders

Treatment

Testosterone Cypionate 100 MG/ML

Clinical Study ID

NCT05487794
DGO-777
  • Ages 18-40
  • Female
  • Accepts Healthy Volunteers

Study Summary

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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

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

Exclusion

Exclusion Criteria:

  • TM with polycythemia vera or secondary to other pathologies (chronic kidney disease,severe lung disease, chronic myeloid leukemia, lymphoma, liver diseases andCushing's syndrome);

  • TM in use of hormonal contraceptives or copper IUDs;

  • TM with psychiatric conditions such as severe psychotic disorders, severepersonality disorders

  • Patients with Ht > 54.

Study Design

Total Participants: 46
Treatment Group(s): 1
Primary Treatment: Testosterone Cypionate 100 MG/ML
Phase:
Study Start date:
September 01, 2022
Estimated Completion Date:
December 17, 2024

Connect with a study center

  • Faculdade de Medicina de Ribeirão Preto - FMRP-USP

    Ribeirão Preto, SP
    Brazil

    Site Not Available

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