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Osteoporosis clinical trials

View clinical trials related to Osteoporosis.

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NCT ID: NCT00352170 Completed - Osteoporosis Clinical Trials

Calcium and Vitamin D Malnutrition in Elderly Women

Start date: May 2000
Phase: Phase 3
Study type: Interventional

This study is designed to test whether calcium supplementation alone or calcium plus vitamin D reduces the incidence of fractures, reduces high parathyroid secretory activity, and halts bone loss in a population-based sample of women 55+ years of age. - A calcium supplement of 1400 mg/d will significantly reduce the cumulative incidence of spine and appendicular fractures over four years for independently living, rural women 55 years of age and older compared to similar women on their usual diets. - A calcium supplement of 1400 mg/d plus 1100 IU vitamin D/d will significantly reduce the cumulative incidence of spine and appendicular fractures compared to a calcium supplement only.

NCT ID: NCT00347737 Withdrawn - Osteoporosis Clinical Trials

The Effects of Therapy With Teriparatide on Vascular Compliance and Osteoprotegerin/RANKL

Start date: June 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to determine what effect teriparatide will have on vascular (blood vessel) compliance and osteoprotegerin (bone fluid)and RANKL levels (bone cells).

NCT ID: NCT00346658 Completed - Osteoporosis Clinical Trials

Magnesium Supplementation to Prevent Bone Loss

Start date: July 2002
Phase: Phase 1
Study type: Interventional

Extreme magnesium deficiency is known to have an impact on the synthesis, secretion and/or action of calcium regulating hormones. Many older adults are at risk for less severe magnesium deficiency, since the majority of adults receive less than the Recommended Daily Allowance of magnesium. We hypothesize that magnesium supplementation will have a beneficial effect on calcium regulating hormones and markers of bone turnover.

NCT ID: NCT00346190 Recruiting - Osteoporosis Clinical Trials

The Study of the Early Administration of Alendronate on Prevention of Bone Loss After Hip Fracture.

Start date: January 2003
Phase: Phase 3
Study type: Interventional

To determine whether administration of Alendronate early is more effective than late in the prevention of osteoporosis following a hip fracture

NCT ID: NCT00345644 Completed - Osteoporosis Clinical Trials

Risedronate in Osteopenic Postmenopausal Women

OSMAUSE
Start date: March 2006
Phase: Phase 3
Study type: Interventional

The primary objective of this study is to compare risedronate 35 mg and placebo with respect to the percent change at 12 months for distal radius trabecular bone volume (BV/TV) in osteopenic postmenopausal women, as measured by three-dimensional peripheral quantitative computed tomography (3D pQCT). The secondary objectives are to compare the percent change from Screening/Baseline between the 2 treatment groups for the following measurements: - Bone mineral density of the lumbar spine, femoral neck, femoral trochanter, and total proximal femur using a dual energy X-ray absorptiometry (DXA) scan at 12 and 24 months; - 3D pQCT analysis of distal radius and distal tibia bone microarchitecture data at 6, 12, and 24 months; and - Bone turnover markers (BTMs) of: - fasting serum carboxyterminal cross linking telopeptide of type 1 bone collagen (CTX 1); - serum aminoterminal propeptide of type 1 procollagen (PINP); and - urine N-telopeptide cross-links (NTX) at 3, 6, 12, and 24 months.

NCT ID: NCT00343252 Completed - Back Pain Clinical Trials

Effect of Teriparatide Compared to Risedronate on Back Pain in Women With a Spine Fracture Caused by Osteoporosis

Start date: June 2006
Phase: Phase 3
Study type: Interventional

The purpose of the study is to determine if daily teriparatide reduces back pain more effectively than weekly risedronate in women with osteoporosis who have chronic back pain due to a spinal bone fracture.

NCT ID: NCT00336232 Completed - Aging Clinical Trials

Determinants of Vitamin K Metabolism

Start date: May 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to learn how the body responds to different amounts of vitamin K in the diet in order to understand the roles that vitamin K may have in the body. We also need to determine if older adults need more or less vitamin K in their diet compared to younger adults in order to maintain normal body stores of vitamin K.

NCT ID: NCT00332709 Completed - Osteoporosis Clinical Trials

Safety/Efficacy of Letrozole Monotherapy or in Combination With Zoledronic Acid as Extended Adjuvant Treatment of Postmenopausal Patients With Primary Breast Cancer

Start date: January 2006
Phase: Phase 3
Study type: Interventional

This was a prospective, randomized, open-label, two arm phase III trial designed to evaluate the efficacy and safety of zoledronic acid in preventing bone loss in postmenopausal women with operable breast cancer who had received 4 to 6 years of adjuvant tamoxifen therapy after resection of the tumor. Patients were treated with letrozole 2.5 mg orally per day or letrozole 2.5 mg orally per day in combination with zoledronic acid 4 mg/6 months as an infusion. This trial did not recruit patients in the United States.

NCT ID: NCT00330538 Completed - Clinical trials for Leukemia, Lymphocytic, Acute, L1

Osteoporosis in Children With ALL

Start date: March 2004
Phase: N/A
Study type: Observational

Hypothesis: Pediatric patients with acute lymphoblastic leukemia, treated with chronic glucocorticoids as a part of the leukemia treatment protocol, will have an increased incidence and severity of osteoporosis.

NCT ID: NCT00330460 Completed - Osteoporosis Clinical Trials

A Randomized, Double-Blind Study to Compare the Efficacy of Treatment With Denosumab Versus Alendronate Sodium in Postmenopausal Women With Low Bone Mineral Density.

Start date: May 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether in postmenopausal women with low bone mineral density, the mean percent change in total hip BMD in subjects receiving denosumab is not less than that observed in subjects receiving alendronate sodium by more than a pre-specified non-inferiority margin.