The Effects of Inhaled Glucocorticoids on the Postmenopausal Skeleton
Primary Purpose
Osteoporosis
Status
Withdrawn
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Budesonide
Placebo Inhaler
Sponsored by
About this trial
This is an interventional other trial for Osteoporosis focused on measuring Osteoporosis, Glucocorticoids, Postmenopausal
Eligibility Criteria
Inclusion Criteria:
- Age ≥ 60 years or at least > 5 years postmenopause (defined as 1 year without a menstrual period)
- No asthma and no history of GC use, either oral or inhaled
Exclusion Criteria:
- Use of oral GCs for > 4 weeks per year in the past 3 years
- History of smoking, to rule out overlapping chronic obstructive pulmonary disease (COPD)
- Other metabolic bone diseases (e.g. hyperparathyroidism, Paget's disease, osteogenesis imperfecta)
- Gastrointestinal Disease (malabsorption, celiac disease, inflammatory bowel disease)
- Endocrinopathies (i.e. untreated thyroid disease, Cushing's syndrome, prolactinoma,)
- Current use of osteoporosis medication (hormone replacement therapy (HRT), raloxifene, bisphosphonates, denosumab)
- Current or past use of teriparatide
- estimated glomerular filtration rate (eGFR)< 45 ml/min calculated by MDRD112 to accommodate mild declines in renal function due to aging
- History of malignancy, except for cured skin cancers
- Diabetes, (HbA1c>6) as this disease is also associated with decreased bone formation
- Osteoporosis by Dual-energy X-ray Absorptiometry (DXA) at any site or an asymptomatic vertebral fracture
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Placebo Comparator
Arm Label
Budesonide 360 mcg
Budesonide 720 mcg
Placebo
Arm Description
Budesonide dry powder inhaler 2 puffs of 90 mcg twice daily for 4 weeks
Budesonide dry powder inhaler 2 puffs of 180 mcg twice daily for 4 weeks
Placebo inhaler 2 puffs twice daily for 4 weeks
Outcomes
Primary Outcome Measures
Change in Osteocalcin
The primary outcome will be the within-group change in serum osteocalcin from baseline to 4-weeks based on intention-to-treat analyses.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02357277
Brief Title
The Effects of Inhaled Glucocorticoids on the Postmenopausal Skeleton
Official Title
The Effects of Inhaled Glucocorticoids on the Postmenopausal Skeleton
Study Type
Interventional
2. Study Status
Record Verification Date
July 2017
Overall Recruitment Status
Withdrawn
Why Stopped
Lack of funding
Study Start Date
March 2015 (undefined)
Primary Completion Date
November 2017 (Anticipated)
Study Completion Date
November 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Columbia University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
There are over 10 million individuals with asthma using inhaled glucocorticoids (IGCs) in the United States. While oral GCs are recognized to have destructive skeletal effects, far less is known about the effects of IGCs. This gap in our knowledge is of critical importance, not only because of the prevalence, chronic nature and long duration of IGC use, but also because several studies have found that patients using IGCs are at increased risk of fracture. Fracture risk is greatest in postmenopausal (PM) women, in whom IGCs may augment negative effects of estrogen loss and aging.
The investigators hypothesize that initiation of IGCs in IGC naïve PM women will lead to decreased bone formation and uncoupling of bone turnover, a potential mechanism for the effect of IGCs on the skeleton.
To test our hypothesis, the investigators will perform a randomized, controlled 4 week study of the acute effects of commonly used doses of budesonide (360 or 720 mcg) on bone turnover and circulating osteoblast precursors in 60 treatment naïve, non-asthmatic, PM women. These studies are of high clinical significance because there are currently no guidelines regarding screening, prevention or treatment for osteoporosis in patients using IGCs, nor is IGC use taken into account when calculating fracture risk in PM women, the group at highest risk of fracture. High quality evidence for low volumetric bone mineral density (BMD) and abnormal bone quality in PM women using IGCs has the potential to change clinical practice by supporting specific interventions to prevent bone loss and fractures.
Detailed Description
The investigators will study acute biochemical and hormonal responses over 4 weeks to commonly prescribed moderate and high doses of budesonide one of the most widely prescribed IGCs, and the preferred drug for Medicare and Medicaid. Sixty treatment naïve PM non-asthmatic women will be randomized to one of 3 groups (20/group): placebo, budesonide 360 or 720 mcg/day. IGCs will be self-administered as 2 puffs twice daily. Budesonide will be provided as Pulmicort flexhaler. At the baseline visit, subjects will be taught proper technique for self-administration of the inhaled medications, including mouth rinsing after each dose. Since dry powder formulations will be used, spacer devices are not required. Women will be assessed at baseline, 1,2, and 4 weeks. This time period and schedule was chosen to ensure adequate time for IGCs to reach peak levels, and to assess the bone metabolic response. Given the 4-6 hr half-life of budesonide, steady state pharmacokinetics will be reached at one week. The investigators will monitor medication adherence using the inhaler's device counter. Visits will be conducted in the Metabolic Bone Diseases Unit. To measure systemic absorption, serum steroid levels will be directly measured.To assess the effects of IGC and dose on the hypothalamic-pituitary-adrenal (HPA) axis, morning (AM) cortisol will be measured at each visit and urinary free cortisol at baseline and 4 weeks.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoporosis
Keywords
Osteoporosis, Glucocorticoids, Postmenopausal
7. Study Design
Primary Purpose
Other
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Budesonide 360 mcg
Arm Type
Experimental
Arm Description
Budesonide dry powder inhaler 2 puffs of 90 mcg twice daily for 4 weeks
Arm Title
Budesonide 720 mcg
Arm Type
Experimental
Arm Description
Budesonide dry powder inhaler 2 puffs of 180 mcg twice daily for 4 weeks
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo inhaler 2 puffs twice daily for 4 weeks
Intervention Type
Drug
Intervention Name(s)
Budesonide
Other Intervention Name(s)
Pulmicort flexhaler
Intervention Description
inhaled glucocorticoid budesonide as dry powder inhaler
Intervention Type
Other
Intervention Name(s)
Placebo Inhaler
Intervention Description
inhaled placebo
Primary Outcome Measure Information:
Title
Change in Osteocalcin
Description
The primary outcome will be the within-group change in serum osteocalcin from baseline to 4-weeks based on intention-to-treat analyses.
Time Frame
Baseline and 4 weeks
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Age ≥ 60 years or at least > 5 years postmenopause (defined as 1 year without a menstrual period)
No asthma and no history of GC use, either oral or inhaled
Exclusion Criteria:
Use of oral GCs for > 4 weeks per year in the past 3 years
History of smoking, to rule out overlapping chronic obstructive pulmonary disease (COPD)
Other metabolic bone diseases (e.g. hyperparathyroidism, Paget's disease, osteogenesis imperfecta)
Gastrointestinal Disease (malabsorption, celiac disease, inflammatory bowel disease)
Endocrinopathies (i.e. untreated thyroid disease, Cushing's syndrome, prolactinoma,)
Current use of osteoporosis medication (hormone replacement therapy (HRT), raloxifene, bisphosphonates, denosumab)
Current or past use of teriparatide
estimated glomerular filtration rate (eGFR)< 45 ml/min calculated by MDRD112 to accommodate mild declines in renal function due to aging
History of malignancy, except for cured skin cancers
Diabetes, (HbA1c>6) as this disease is also associated with decreased bone formation
Osteoporosis by Dual-energy X-ray Absorptiometry (DXA) at any site or an asymptomatic vertebral fracture
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Emily M Stein, MD
Organizational Affiliation
Columbia University
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
The Effects of Inhaled Glucocorticoids on the Postmenopausal Skeleton
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