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Osteoporosis clinical trials

View clinical trials related to Osteoporosis.

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NCT ID: NCT01293487 Completed - Osteoporosis Clinical Trials

Safety And Tolerability Study Of RN564 In Women With Osteopenia And Healthy Men.

Start date: April 2011
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the safety and tolerability of RN564 in women with osteopenia and healthy men.

NCT ID: NCT01293292 Completed - Osteoporosis Clinical Trials

Teriparatide (Forsteo) Treatment in Postmenopausal Women: Mechanism of Action

Forsteo
Start date: January 2011
Phase: Phase 4
Study type: Interventional

Previously the approach to treatment of osteoporosis has been to use medications which prevent excessive resorption of bone. More recently medications that build up new bone, i.e. anabolic treatments, have been, and are being, developed. The investigators would like to develop a strategy for evaluating the effectiveness of anabolic therapies by studying a currently available therapy (teriparatide). This strategy could then be used to assess new anabolic treatments as they are developed for use in humans. The aims of this study are 1) to fully describe the changes in bone turnover in response to teriparatide by biochemical marker type and by time; 2) to fully describe the changes in bone mineral density (BMD) in response to teriparatide by site, bone compartment and time. If this study is able to identify an early response to treatment, then this will help speed up drug development in this area, by allowing the identification of promising new anabolic drugs and enabling us to understand their mechanism of action. This will benefit the investigators patients as the investigators will have a better understanding of how these drugs work.

NCT ID: NCT01293045 Completed - Osteoporosis Clinical Trials

Biological Bone Markers and Hydrolyzed Collagen Supplement in Menopausal Healthy Women

Start date: June 2010
Phase: Phase 1
Study type: Interventional

- Preliminary scientific studies, in both animals and humans suggest that oral consumption of hydrolyzed collagen acts on the bone remodeling process by stimulating the activity of osteoblasts responsible for bone formation while improving the bone mineral density and biomechanical resistance of long bones. - The objective of this clinical research is to measure changes in biomarkers of bone turnover in postmenopausal healthy women, not osteoporotic, in response to consumption of hydrolyzed collagen for three months. - For this, we propose to measure blood and urinary markers of formation and bone resorption before consumption, then 45 and 90 days after daily consumption of 10 g of hydrolyzed collagen.

NCT ID: NCT01292187 Completed - Osteopenia Clinical Trials

A Study of Oral Recombinant Salmon Calcitonin (rsCT) to Prevent Postmenopausal Osteoporosis

Start date: January 2011
Phase: Phase 2
Study type: Interventional

The primary purpose of this study was to evaluate the efficacy of oral calcitonin (rsCT)tablets in the prevention of bone loss in postmenopausal women with lower bone mineral density at increased risk of fracture. The secondary purpose of this study was to determine if there is any food effect by comparing the efficacy and safety of oral calcitonin tablets administered at dinner or at bedtime.

NCT ID: NCT01290094 Completed - Clinical trials for Post Menopausal Osteoporosis

A Study of Bonviva/Boniva (Ibandronate) in Biphosphonate-Naïve Women With Post-Menopausal Osteoporosis

Start date: April 2011
Phase: Phase 3
Study type: Interventional

This single arm, open label study will assess the efficacy and safety of and compliance to treatment with Bonviva/Boniva (ibandronate) in biphosphonate-naïve patients with post-menopausal osteoporosis. Patients will receive Bonviva/Boniva at a dose of 3 mg intravenously every three months. Anticipated time on study treatment is 12 months with a follow-up of 12 months.

NCT ID: NCT01287533 Completed - Clinical trials for Rheumatoid Arthritis

Efficacy of Monthly Ibandronate in Women With RA and Reduced Bone Mineral Density Receiving Long-term Steroids

Start date: April 2010
Phase: Phase 4
Study type: Interventional

This study was to investigate the efficacy of oral monthly ibandronate in the management of glucocorticoid induced osteoporosis in women with rheumatoid arthritis.

NCT ID: NCT01277562 Completed - Breast Cancer Clinical Trials

Pilot Study of Secondary Causes of Osteopenia/Osteoporosis in Adults With Breast and Prostate Cancer

Start date: November 2010
Phase: N/A
Study type: Observational

The investigators hypothesis is that secondary causes of bone loss are prevalent in patients with breast and prostate cancer, and those patients with secondary causes of bone loss are at higher risk for treatment related bone loss. The goals of this pilot study are to estimate the prevalence of secondary causes of osteoporosis in a cohort of patients with nonmetastatic breast and prostate cancer with osteopenia and osteoporosis.

NCT ID: NCT01277185 Completed - Osteoporosis Clinical Trials

Calcium Metabolism in Mexican American Adolescents

Start date: April 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to identify calcium metabolism characteristics in Mexican American adolescents. The investigators predict that calcium requirements to maximize bone health in this population will be lower than for white youth but higher than their current intakes.

NCT ID: NCT01267279 Completed - Osteoporosis Clinical Trials

Effect of Zoledronic Acid on Femoral Bone Loss Following Total Hip Arthroplasty

Start date: January 2005
Phase: Phase 4
Study type: Interventional

In a randomized, double-blind trial, BMD of the operated proximal femur after total hip replacement measured by dual-energy x-ray absorptiometry (DXA) were compared for up to two years in patients receiving IV ZOL 5 mg infusion (n = 27) or placebo (IV saline infusion; n = 24) at two weeks and one year after surgery.

NCT ID: NCT01263847 Completed - Osteoporosis Clinical Trials

Galactooligosaccharide (GOS) Supplementation and Calcium Absorption in Girls

Friesland
Start date: June 2009
Phase: Early Phase 1
Study type: Interventional

The purpose of this study is to determine the effects of galactooligosaccharide (GOS) supplementation on calcium absorption and and gut microbe profiles.