PaTH Study: Parathyroid Hormone and Alendronate for Osteoporosis
Osteoporosis
About this trial
This is an interventional treatment trial for Osteoporosis focused on measuring PTH, Alendronate, Parathyroid hormone, Osteoporosis, Postmenopausal
Eligibility Criteria
Inclusion Criteria: Aged between 55 and 85 years Postmenopausal (have not had any menses in the last 5 years) Have a bone mineral density scan (DXA) that can be evaluated at the spine AND at the hip with a T-score equal to or below -2.5 at the spine or the femoral neck or total hip OR T-score equal to or below -2.0 at the spine or the femoral neck or total hip and have at least one of the following risk factors for fracture: (a) age > 65 years; (b) history of postmenopausal fracture (nonvertebral or vertebral); or (c) maternal history of hip fracture Willing and able to self-administer daily injections Exclusion Criteria: Have used estrogen (oral or patch) for more than 1 month in the last 6 months or more than 12 months in the last 2 years History of more than 12 months of bisphosphonate use ever, or any use (> 4 weeks) within the past 12 months History of rhPTH (recombinant human PTH) use Any major life-threatening illnesses Type 1 or uncontrolled type 2 diabetes mellitus (defined as hemoglobin A1C > 10.0), or currently using insulin Vitamin D level < 15 nanograms/ml History of kidney disease (creatinine > 2.0 mg/dl) Renal insufficiency (creatinine clearance < 40 mg/min) Any history of kidney stones Any history of hypercalciuria or currently have urine calcium/creatinine >300 mg History of hypercalcemia, sarcoidosis, or hyperparathyroidism History of active or treated tuberculosis or other granulomatous disorders History of breast cancer, melanoma, or hematologic malignancy that has required treatment within the last 10 years History of bone cancer or any other metabolic bone disease that has required treatment within the last 10 years History of any other nonskin cancer that has required treatment within the last 10 years History of symptomatic esophageal reflux, achalasia or esophageal stricture Currently taking > 7.5 mg systemic prednisone or equivalent per day Currently using > two puffs, four times/day of inhaled steroids Currently taking anticoagulants or anticonvulsants Have used Calcitonin within the past 3 months Have used Raloxifene in the last 6 months or for more than 12 months in the last 2 years Have used Tamoxifen in the last 6 months or for more than 12 months in the last 2 years Have used fluoride for at least a month within the past 5 years Currently taking > 1000 IU/day vitamin D or vitamin D analogues or metabolites Currently taking thyroid hormone replacement AND have a TSH < 0.1mIU/L
Sites / Locations
- Maine Center for Osteoporosis
- University of Minnesota
- Columbia University
- University of Pittsburgh Medical Center
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Experimental
Experimental
Experimental
Active Comparator
1
2
3
4
Participants will receive PTH for 1 year followed by alendronate for 1 year.
Participants will receive PTH and alendronate for 1 year followed by alendronate for 1 year.
Participants will receive alendronate for 2 years.
Participants will receive PTH for 1 year followed by placebo for 1 year.