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
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
BrazilSite Not Available
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