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Last Updated: June 4, 2020

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CLINICAL TRIALS PROFILE FOR ALENDRONATE SODIUM

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All Clinical Trials for Alendronate Sodium

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00000412 Osteoporosis Prevention After Heart Transplant Completed Merck Sharp & Dohme Corp. Phase 3 1997-09-01 During the first year after a heart transplant, people often rapidly lose bone from their spine and hips. About 35 percent of people who receive heart transplants will suffer broken bones during the first year after transplantation. This study will compare the safety and effectiveness of the drug alendronate (Fosamax) and the active form of vitamin D (calcitriol) in preventing bone loss at the spine and hip after a heart transplant. In this study, people who have had a successful heart transplant will receive either active alendronate and a "dummy pill" instead of calcitriol, or active calcitriol and a dummy pill instead of alendronate for the first year after their transplant, starting within 1 month after transplant surgery. We will measure bone density in the hip and spine at the start of the study and after 6 and 12 months, and will also check for broken bones in the spine. This research should lead to ways of preventing this crippling form of osteoporosis.
NCT00000412 Osteoporosis Prevention After Heart Transplant Completed National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) Phase 3 1997-09-01 During the first year after a heart transplant, people often rapidly lose bone from their spine and hips. About 35 percent of people who receive heart transplants will suffer broken bones during the first year after transplantation. This study will compare the safety and effectiveness of the drug alendronate (Fosamax) and the active form of vitamin D (calcitriol) in preventing bone loss at the spine and hip after a heart transplant. In this study, people who have had a successful heart transplant will receive either active alendronate and a "dummy pill" instead of calcitriol, or active calcitriol and a dummy pill instead of alendronate for the first year after their transplant, starting within 1 month after transplant surgery. We will measure bone density in the hip and spine at the start of the study and after 6 and 12 months, and will also check for broken bones in the spine. This research should lead to ways of preventing this crippling form of osteoporosis.
NCT00000412 Osteoporosis Prevention After Heart Transplant Completed Columbia University Phase 3 1997-09-01 During the first year after a heart transplant, people often rapidly lose bone from their spine and hips. About 35 percent of people who receive heart transplants will suffer broken bones during the first year after transplantation. This study will compare the safety and effectiveness of the drug alendronate (Fosamax) and the active form of vitamin D (calcitriol) in preventing bone loss at the spine and hip after a heart transplant. In this study, people who have had a successful heart transplant will receive either active alendronate and a "dummy pill" instead of calcitriol, or active calcitriol and a dummy pill instead of alendronate for the first year after their transplant, starting within 1 month after transplant surgery. We will measure bone density in the hip and spine at the start of the study and after 6 and 12 months, and will also check for broken bones in the spine. This research should lead to ways of preventing this crippling form of osteoporosis.
NCT00004488 Phase II Randomized Study of Alendronate Sodium for Osteopenia in Patients With Gaucher's Disease Completed Children's Hospital Medical Center, Cincinnati Phase 2 1998-10-01 OBJECTIVES: I. Determine the efficacy of alendronate sodium in treating osteopenia (generalized bone density and focal bone lesions) in patients with Gaucher's disease.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Alendronate Sodium

Condition Name

Condition Name for Alendronate Sodium
Intervention Trials
Osteoporosis 10
Healthy 4
Postmenopausal Osteoporosis 3
Osteopenia 2
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Condition MeSH

Condition MeSH for Alendronate Sodium
Intervention Trials
Osteoporosis 16
Osteoporosis, Postmenopausal 5
Bone Diseases, Metabolic 2
Periodontitis 1
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Clinical Trial Locations for Alendronate Sodium

Trials by Country

Trials by Country for Alendronate Sodium
Location Trials
United States 12
Israel 1
Denmark 1
Canada 1
United Kingdom 1
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Trials by US State

Trials by US State for Alendronate Sodium
Location Trials
North Dakota 3
South Carolina 2
New York 2
Wisconsin 1
Colorado 1
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Clinical Trial Progress for Alendronate Sodium

Clinical Trial Phase

Clinical Trial Phase for Alendronate Sodium
Clinical Trial Phase Trials
Phase 4 3
Phase 3 9
Phase 2 6
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Clinical Trial Status

Clinical Trial Status for Alendronate Sodium
Clinical Trial Phase Trials
Completed 20
Recruiting 2
Terminated 1
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Clinical Trial Sponsors for Alendronate Sodium

Sponsor Name

Sponsor Name for Alendronate Sodium
Sponsor Trials
Merck Sharp & Dohme Corp. 10
Medical University of South Carolina 2
Mylan Pharmaceuticals 2
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Sponsor Type

Sponsor Type for Alendronate Sodium
Sponsor Trials
Industry 17
Other 12
NIH 3
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