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Osteoporosis clinical trials

View clinical trials related to Osteoporosis.

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NCT ID: NCT00963417 Active, not recruiting - Breast Cancer Clinical Trials

Study of Bone Mineral Density in Women With Breast Cancer Treated With Triptorelin and Tamoxifen or Exemestane on Protocol IBCSG 25-02

TEXT-Bone
Start date: August 3, 2009
Phase: N/A
Study type: Interventional

RATIONALE: Gathering information over time from bone density and laboratory tests of women with breast cancer treated with triptorelin and tamoxifen or exemestane may help the study of breast cancer in the future. PURPOSE: This clinical trial is studying changes in bone mineral density in women with breast cancer treated with triptorelin and tamoxifen or exemestane on protocol IBC SG-25-02 (TEXT).

NCT ID: NCT00759772 Active, not recruiting - Osteoporosis Clinical Trials

The Role of Parathyroid Hormone (PTH) in Low Bone Mass in Anorexia Nervosa

Start date: September 2008
Phase: Phase 2
Study type: Interventional

Decreased bone strength is a common and serious medical problem present in many women with anorexia nervosa, or disordered eating. Women with decreased bone strength are more likely to suffer broken bones than women with normal bone strength. We are investigating whether a hormone that is naturally produced by the human body -- parathyroid hormone (PTH) -- can help strengthen the bones of women with anorexia nervosa.

NCT ID: NCT00689923 Active, not recruiting - Osteoporosis Clinical Trials

Vertebroplasty Using Real-Time, Fluoroscopy-Controlled, Catheter-Assisted, Low-Viscosity Cement Injection

Start date: November 2007
Phase: N/A
Study type: Observational

Th low viscosity cement injection is safe in vertebroplasty procedure with Comparacle out come in pain relief.

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: NCT00634686 Active, not recruiting - Osteoporosis Clinical Trials

Effects of Omega-3 Fatty Acids on Bone and Frailty

Start date: January 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to examine the effects of essential fatty acid (EFA) supplementation on bone metabolism and frailty in postmenopausal women. The overall hypothesis is that EFA supplementation, via its immunoregulatory and anti-inflammatory activity, will decrease bone turnover, decrease prostaglandins and cytokines associated with bone metabolism and frailty, and change physical outcome measures associated with frailty in postmenopausal women with low bone mass and frailty.

NCT ID: NCT00594789 Active, not recruiting - Osteoporosis Clinical Trials

Closing The Post Fracture Care Gap In Manitoba

Start date: June 2008
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate a post-fracture intervention for improving osteoporosis care in older men and women who have suffered a fracture that may indicate the presence of osteoporosis. Although osteoporosis can be identified with a bone mineral density (BMD) test, most individuals with osteoporosis are not diagnosed until they fracture. Post-fracture care often "falls between the cracks" when there is a breakdown in communication between hospital and community, or between specialists and primary care physicians. Often physicians and patients fail to make the connection between an acute fracture and osteoporosis, or the value of secondary prevention strategies. If untreated, there is an extremely high rate of additional fractures after a first osteoporotic fracture. It follows that improving BMD testing and/or treatment in appropriately identified individuals is a necessary step in optimizing post-fracture patient care. Over the next three years we will be testing and optimizing a notification procedure to physicians and/or patients relying upon fracture events reported to the provincial health service (Manitoba Health).

NCT ID: NCT00414830 Active, not recruiting - Osteoporosis Clinical Trials

Systematic Prevention of Further Fractures in Patients With Hip Fractures and Osteoporosis.

Start date: January 2005
Phase: N/A
Study type: Observational

The purpose of this study is to determine if prevention of further fractures is possible through systematic evaluation for osteoporosis in patients with recent hip fracture

NCT ID: NCT00359047 Active, not recruiting - Osteoporosis Clinical Trials

Recognizing Osteoporosis and Its Consequences in Quebec (ROCQ) Programme

Start date: June 2003
Phase: N/A
Study type: Interventional

The aim of the ROCQ programme is to improve the use of evidence based osteoporosis diagnostic and treatment strategies for women 50 years and over who have suffered a fragility fracture. This objective will be achieved by concentrating on a realistic evaluation of the present diagnosis and treatment rate of osteoporosis following a fragility fracture and comparing it to an optimal situation (care gap) and proposing interventions that promote new approaches to treating osteoporosis by health professionals as well as providing targeted interventions for the patient. The efficacy of these interventions will be evaluated using a randomized control design.

NCT ID: NCT00302484 Active, not recruiting - Osteoporosis Clinical Trials

Use of Bisphosphonates in the Treatment of Osteopathy After Liver Transplantation

Start date: April 2002
Phase: N/A
Study type: Interventional

Patients with a terminal chronic liver disease have a disordered bone metabolism resulting in a higher risk of falling ill with osteoporosis. Although liver transplantation restores liver function, immunosuppressive therapy (especially corticosteroids) after transplantation increases again the risk of osteoporosis and bone fragility. Zoledronate, a bisphosphonate, slows down the destruction of bone. The purpose of this study is to determine whether bisphosphonates are effective in the prevention of osteoporosis following immunosuppressive therapy after liver transplantation.

NCT ID: NCT00209469 Active, not recruiting - Osteoporosis Clinical Trials

Network Osteoporosis Study

Start date: July 2002
Phase: Phase 2/Phase 3
Study type: Interventional

This study is evaluating the use of the drug alendronate in preventing or reversing bone loss in children and adolescents receiving steroid medications.