CT-Based Changes in Bone and Marrow Among Patients on Oral Steroids
Stopped early
Conditions studied: Asthma, Bone Density, Low, Oral Steroid-Dependent Asthma (Disorder)
In brief
The goal of this study is to assess the feasibility of emerging CT-based tools to measure changes in central and peripheral bone density, micro-structure, and marrow adipose tissue (MAT) among patients treated with oral steroids.
Key facts
- Study ID
- NCT04518722
- Run by
- University of Iowa
- People needed
- 2
- Starts
- 2020-12-01
- Expected to finish
- 2021-09-28
- Last updated by the study team
- 2026-04-07
Who can join
Age: 25 and older, up to 45. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Inclusion (all subjects):
- Diagnosis of severe, persistent asthma (defined as using both a long-acting beta-agonist AND a high-dose inhaled steroid)
- Age 25-45
- Inclusion (oral steroid group):
- Chronic treatment with oral steroids for at least 45 days but less than 1 year
You may not qualify if…
- Exclusion (all subjects):
- Pregnant or breastfeeding
- History of any cancer, excluding non-melanoma skin cancer
- Currently receiving dialysis
- History of any lower extremity fracture
- Hip or knee replacement
- Non-ambulatory
- Greater than 10 pack-year smoking history
- BMI > 50
- Age < 25 or > 45
- Current or past use of FDA-approved medication for osteoporosis:
- Bisphosphonates (Alendronate/Fosamax, Ibandronate/Boniva, Risedronate/Actonel/Atelvia, Zoledronic Acid/Reclast) Calcitonin (Fortical, Miacalcin) Selective Estrogen Receptor Modulator (Raloxifene/Evista) Parathyroid Hormone Analogue (Teriparatide/Forteo) Monoclonal Antibody (Denosumab/Prolia)
Where it is running
- University of Iowa — Iowa City, Iowa, United States
Full record on ClinicalTrials.gov
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