Skeletal Health and Bone Marrow Composition Among Youth

NAActive, not recruitingINTERVENTIONAL
Enrollment

80

Participants

Timeline

Start Date

September 15, 2020

Primary Completion Date

December 30, 2025

Study Completion Date

December 30, 2025

Conditions
Gender Dysphoria in ChildrenPubertyBone Development
Interventions
DEVICE

GnRH Agonist

Forty participants who are transgender and who have been prescribed a gonadotropin-releasing hormone (GnRH) agonist by their physician will undergo magnetic resonance imaging (MRI), magnetic resonance spectroscopy (MRS), dual-energy x-ray absorptiometry (DXA) and peripheral quantitative computed tomography (pQCT) scans at baseline, at 12 months and at 24 months after initiation of the GnRH agonist therapy. This longitudinal observational study of two cohorts seeks to identify significant changes in bone marrow adiposity and bone density over 24 months. The same assessments will be obtained in 40 healthy control subjects matched for age, race/ethnicity and body mass index, all factors that are known to influence skeletal outcomes. The evaluations of bone marrow adiposity will be correlated with bone density measurements and the assessments of mood (validated anxiety and depression scales) and health-related quality of life, before and after pubertal blockade.

Trial Locations (2)

45229

Cincinnati Children's Hospital Medical Center, Cincinnati

02215

Boston Children's Hospital, Boston

All Listed Sponsors
collaborator

Children's Hospital Medical Center, Cincinnati

OTHER

lead

Amy DiVasta, MD

OTHER