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Osteoporosis clinical trials

View clinical trials related to Osteoporosis.

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NCT ID: NCT00680953 Completed - Osteoporosis Clinical Trials

Denosumab Fracture Intervention Randomized Placebo Controlled Trial in Japanese Patients With Osteoporosis

DIRECT
Start date: May 2008
Phase: Phase 3
Study type: Interventional

Evaluate the efficacy and safety of denosumab in the treatment of involutional (postmenopausal and senile) osteoporotic subjects with prevalent fragility vertebral fracture(s)

NCT ID: NCT00679198 Completed - Osteoporosis Clinical Trials

Improving Osteoporosis Care in High-Risk Home Health Patients

Start date: March 2009
Phase: N/A
Study type: Interventional

SPECIFIC AIMS: We propose a three-year study to develop a high-intensity intervention to improve osteoporosis care and test a novel intervention in a group-randomized trial of 27 home health offices and 1,000 patients referred to home health care with a history of fracture. Aim 1. Develop an intervention to promote osteoporosis treatment that includes: (1) training to enhance nurse-patient and nurse-physician risk communication regarding osteoporosis and fracture risk; (2) automated prompts within the home health agency's electronic medical record system to promote appropriate osteoporosis management; and (3) implementation of osteoporosis-related standardized care pathways and order sets. Aim 2. Conduct a group-randomized trial to test the effectiveness of the intervention to promote initial use of osteoporosis medications and adherence to treatment after discharge from home health. We hypothesize that: H1: Patients in the intervention group will have increased initial receipt of osteoporosis prescription medications and calcium/vitamin D supplements to prevent and treat osteoporosis compared to patients receiving usual care; H2: Patients in the intervention group will demonstrate increased persistence in the use of these therapies compared to those receiving usual care. Secondary Aims (SA) will include exploratory analyses of fracture related morbidity and mortality, patient-reported quality of life, and health services utilization and costs.

NCT ID: NCT00676312 Completed - Clinical trials for Postmenopausal Osteoporosis

Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Effect of PTH134 at Increasing Doses in Healthy Postmenopausal Subjects

Start date: May 2008
Phase: Phase 1
Study type: Interventional

This study is designed to investigate the safety and tolerability of PTH134 in healthy subjects and to assess the exposure from PTH134.

NCT ID: NCT00675688 Completed - Osteoporosis Clinical Trials

Study Evaluating Safety and Efficacy of Bazedoxifene/Conjugated Estrogens Combinations in Postmenopausal Women

Start date: April 2002
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether bazedoxifene/conjugated estrogens combinations are effective for the prevention of endometrial hyperplasia and for the prevention of osteoporosis in postmenopausal women.

NCT ID: NCT00674453 Completed - Bone Loss Clinical Trials

The Prevention Of Postmenopausal Osteoporosis With Lasofoxifene And Cytokine Evaluation

LACE
Start date: September 2004
Phase: Phase 2
Study type: Interventional

The objective of the study is to demonstrate the effects that lasofoxifene has on serum markers of bone metabolism.

NCT ID: NCT00671944 Completed - Osteoporosis Clinical Trials

Long-term Nutritional Intervention Study to Determine How Protein Affects Calcium Metabolism

Start date: May 2003
Phase: Phase 1
Study type: Interventional

Osteoporosis is a major health problem in men and women in this country and the incidence of this disease is rising. We think that environmental factors such as nutrition may play a role in the increasing prevalence of osteoporosis. In particular, we think that a diet that is too low in protein may be contributing to bone loss. The primary purpose of this study is to compare the long-term impact of a low protein diet on measures of bone and calcium metabolism.

NCT ID: NCT00670501 Completed - Clinical trials for Osteoporosis, Postmenopausal

Effects of Teriparatide in the Treatment of Postmenopausal Women With Osteoporosis

Start date: August 1996
Phase: Phase 3
Study type: Interventional

The primary objective of this study is to demonstrate a reduction in the proportion of new vertebral fractures in postmenopausal women with osteoporosis following 3-years of treatment with 20 and 40 mcg/day of teriparatide plus calcium and vitamin D compared with calcium and vitamin D alone.

NCT ID: NCT00670319 Completed - Clinical trials for Osteoporosis, Postmenopausal

Comparison of Raloxifene Hydrochloride and Placebo in the Treatment of Postmenopausal Women With Osteoporosis

MORE
Start date: November 1994
Phase: Phase 3
Study type: Interventional

To study the effect of long-term treatment with raloxifene, compared with placebo, on the rate of new vertebral fractures in osteoporotic postmenopausal women with and without existing vertebral fractures.

NCT ID: NCT00668941 Active, not recruiting - Osteoporosis Clinical Trials

Cyclic Versus Daily Teriparatide on Bone Mass

Start date: September 2005
Phase: Phase 2
Study type: Interventional

Osteoporosis is a disease that affects millions of individuals in the United States and abroad. It leads to decreased bone mass and causes an increased risk of fracture. This study will compare continuous versus cyclic treatment with teriparatide combined with alendronate, another drug for osteoporosis, or teriparatide alone in women with osteoporosis.

NCT ID: NCT00668447 Completed - Osteoporosis Clinical Trials

Soy and Isoflavones Effect on Bone

Start date: November 2001
Phase: Phase 4
Study type: Interventional

The purpose of this study is to test the effect of 1 year of added dietary soy protein and/or soy isoflavones on bone mineral density in late postmenopausal women.