Last updated: January 30, 2024
Sponsor: Walter Reed National Military Medical Center
Overall Status: Active - Recruiting
Phase
N/A
Condition
Hypogonadism
Treatment
Estradiol
Fortesta
Clinical Study ID
NCT06247267
Transgender Study
Ages 18-65 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Male and female DoD health care beneficiaries
- Ages 18-65
- Diagnosed with primary hypogonadism or transgender treatment for at least 6 months
- Under care for gender identity dysphoria
- On stable dose of sex steroid hormonal therapy for at least 6 months prior toenrolling
- Must be living in the Washington, D.C. area for at least 12 months followingenrollment
Exclusion
Exclusion Criteria:
- Pregnancy, plan for pregnancy in the next 12 months
- Cardiac disease, especially coronary artery disease
- Malabsorption disorder
- Gastrointestinal surgeries
- Significant renal or liver dysfunction
- Seizure disorders
- recent orders to move out of the geographic area
- Age less than 18 years old or older than 65 years old
- Scheduled for deployment
Study Design
Total Participants: 75
Treatment Group(s): 2
Primary Treatment: Estradiol
Phase:
Study Start date:
March 01, 2019
Estimated Completion Date:
January 31, 2025
Study Description
Connect with a study center
Walter Reed National Military Medical Center
Bethesda, Maryland 20889-5600
United StatesActive - Recruiting
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