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Study identifier: NCT07010146 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Role of Estrogen on Skeletal Outcomes in FHA

Condition: Bone Strength · Bone Density · FHA (Functional Hypothalamic Amenorrhea)  ·  Sponsor: University of Virginia

PhasePhase 2
Planned participants150
Who can joinFemale, 14 Years to 30 Years
Healthy volunteersNo

About this study

The purpose of this study is to assess whether the natural form of estrogen (17-beta estradiol) given as a patch so that it is absorbed through your skin, is better at improving bone strength over 1 year than natural estrogen (17-beta estradiol) taken by mouth, or a synthetic form oestrogen (ethinyl estradiol) given as a patch that also provides birth control. Participants will: 1. Take estrogen for 1 year either (i) in its natural form as a patch twice a week (and progesterone by mouth for 12 days of each month), or (ii) in its natural form as a pill daily (and progesterone by mouth for 12 days of each month), or (iii) in a synthetic form as a birth control patch weekly for 3 weeks with 1 week off the patch. You will not be able to choose which form of estrogen you will receive as this will be assigned to you based on a pre-existing randomization sequence (like the flip of a coin) 2. Take provided calcium and vitamin D supplements 3. Attend 4 study visits over 12 months with two at the beginning and then every 6 months that include: * History and Physical Exams * Lab Work * Imaging studies * Questionnaires * Dietary recalls

This description comes directly from the study's public registry record.

Talk to the study team

Madhusmita Misra, MD, MPH  ·  434-924-9141  ·  madhusmita.misra@uvahealth.org

Sara Braslow, BA  ·  434-982-4234  ·  EVZ3BW@uvahealth.edu

Always discuss trial participation with your own doctor first.

Locations (2)

University of Virginia Medical CenterCharlottesville, Virginia, United StatesRecruiting
University of VirginiaCharlottesville, Virginia, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07010146