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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Withdrawn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
Columbia University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Osteoporosis focused on measuring Osteoporosis, Glucocorticoids, Postmenopausal

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

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

    First Posted
    February 3, 2015
    Last Updated
    July 14, 2017
    Sponsor
    Columbia University
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    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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