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Journal of Clinical Densitometry
Volume 13, Issue 1
, Pages 56-62
, January 2010
Risedronate on 2 Consecutive Days a Month Reduced Vertebral Fracture Risk at 1
Year Compared With Historical Placebo
References
- Effects of risedronate treatment on vertebral and nonvertebral fractures in women with postmenopausal osteoporosis: a randomized controlled trial. Vertebral Efficacy With Risedronate Therapy (VERT) Study Group. JAMA. 1999;282:1344–1352
- Randomized trial of the effects of risedronate on vertebral fractures in women with established postmenopausal osteoporosis. Vertebral Efficacy With Risedronate Therapy (VERT) Study Group. Osteoporos Int. 2000;11:83–91
- Risedronate therapy prevents corticosteroid-induced bone loss: a twelve-month multicenter, randomized, double-blind, placebo-controlled, parallel-group study. Arthritis Rheum. 1999;42:2309–2318
- Efficacy and safety of daily risedronate in the treatment of corticosteroid-induced osteoporosis in men and women: a randomized trial. European Corticosteroid-Induced Osteoporosis Treatment Study. J Bone Miner Res. 2000;15:1006–1013
- Effects of risedronate treatment on bone density and vertebral fracture in patients on corticosteroid therapy. Calcif Tissue Int. 2000;67:277–285
- Persistent bisphosphonate use and the risk of osteoporotic fractures in clinical practice: a database analysis study. Curr Med Res Opin. 2006;22:1757–1764
- Adherence and persistence associated with the pharmacologic treatment of osteoporosis in a managed care setting. South Med J. 2006;99:570–575
- Compliance and persistence with bisphosphonate dosing regimens among women with postmenopausal osteoporosis. Curr Med Res Opin. 2005;21:1453–1460
- Persistence to bisphosphonate treatment in actual clinical practice. Bone. 2005;37:S412
- Strong patient preference for once-monthly over weekly oral bisphosphonate dosing in postmenopausal osteoporosis. Bone. 2005;37:S417
- Patient preference for once-monthly ibandronate versus once-weekly alendronate in a randomized, open-label, cross-over trial: the Boniva Alendronate Trial in Osteoporosis (BALTO). Curr Med Res Opin. 2005;21:1895–1903
- Monthly dosing of 75 mg risedronate on 2 consecutive days a month: efficacy and safety results. Osteoporos Int. 2008;19:1039–1045
- . Limitations of randomized clinical trials. Proposed alternative designs. Clin Chem Lab Med. 2000;38:1217–1223
- . The ethics of randomized clinical trials. Am J Med. 1987;82:283–290
- Use of matched historical controls to evaluate the anti-fracture efficacy of once-a-week risedronate. Osteoporos Int. 2003;14:437–441
- Effect of alendronate on risk of fracture in women with low bone density but without vertebral fractures: results from the Fracture Intervention Trial. JAMA. 1998;280:2077–2082
- Reduction of vertebral fracture risk in postmenopausal women with osteoporosis treated with raloxifene: results from a 3-year randomized clinical trial. Multiple Outcomes of Raloxifene Evaluation (MORE) Investigators. JAMA. 1999;282:637–645
- Randomised trial of effect of alendronate on risk of fracture in women with existing vertebral fractures. Fracture Intervention Trial Research Group. Lancet. 1996;348:1535–1541
- A randomized trial of nasal spray salmon calcitonin in postmenopausal women with established osteoporosis: the Prevent Recurrence of Osteoporotic Fractures Study. PROOF Study Group. Am J Med. 2000;109:267–276
- . Vertebral fracture assessment using a semiquantitative technique. J Bone Miner Res. 1993;8:1137–1147
- Long-term efficacy of risedronate: a 5-year placebo-controlled clinical experience. Bone. 2003;32:120–126
- The efficacy and tolerability of risedronate once a week for the treatment of postmenopausal osteoporosis. Calcif Tissue Int. 2002;71:103–111
- Efficacy and safety of risedronate 150 mg once a month in the treatment of postmenopausal osteoporosis. Bone. 2008;42:36–42
- . The evaluation of therapies: historical control studies. Stat Med. 1984;3:315–324
- . The combination of randomized and historical controls in clinical trials. J Chronic Dis. 1976;29:175–188
Conflict of interest: Dr. Nelson B. Watts receives honoraria and consulting fees through the University of Cincinnati Bone Health and Osteoporosis Center and research support from Procter & Gamble Pharmaceuticals and sanofi-aventis. Dr. Jacques P. Brown receives honoraria for lecturing and consultancies as well as grants and research support for clinical trials sponsored by sanofi-aventis Canada and Procter & Gamble Pharmaceuticals. Dr. Gary Cline was an employee of Procter & Gamble Pharmaceuticals. He also owns stock in Procter & Gamble Pharmaceuticals.
PII: S1094-6950(09)00234-0
doi: 10.1016/j.jocd.2009.09.005
© 2010 The International Society for Clinical Densitometry. Published by Elsevier Inc. All rights reserved.
« Previous
Next »
Journal of Clinical Densitometry
Volume 13, Issue 1
, Pages 56-62
, January 2010
