Bone Strength

2

Review clinical trials related to Bone Strength. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Role of Estrogen on Skeletal Outcomes in FHA

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

Participants needed: 150
Trial details
Phase: Phase 2Age: 14-30Biological sex: FemaleType: InterventionalSponsor: University of VirginiaUpdated: Apr 17, 2026Locations: 2
Eligibility criteria

Females, age 14-30 years, skeletally mature with bone age ≥ 14 years (only 2% of... [+4]

Disease other than FHA known to affect bone, including untreated thyroid dysfunc... [+9]

Status: Recruiting

Bone Metabolism in 12-21 Year Olds Undergoing Glucagon Like Peptide (GLP)-1 Receptor Agonist Therapy

The goal of this clinical trial is to compare bone health markers over 24 months in participants 12 - 21 years of age with obesity who are starting the glucagon-like peptide-1 receptor agonists (GLP-1RAs) as compared to those with similar weight followed by lifestyle management. Participants will: * Take GLP-1RA as prescribed or continue to work on lifestyle management for weight loss * Take provided calcium and vitamin D supplements * Attend 6 study visits over 24 months with two at the beginning and then every 6 months that include: * History and Physical Exams * Lab Work * Imaging studies * Questionnaires * 24-hour dietary recalls

Participants needed: 120
Trial details
Phase: Phase 2Age: 12-21Biological sex: AllType: InterventionalSponsor: University of VirginiaUpdated: Apr 17, 2026Locations: 1
Eligibility criteria

• Adolescents and young adults with obesity 12-21 years old starting GLP-1 RA th... [+5]

• Current or previous history of pregnancy and breast feeding. [+13]