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Osteoporosis clinical trials

View clinical trials related to Osteoporosis.

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NCT ID: NCT01657162 Completed - Clinical trials for Postmenopausal Osteoporosis

Twenty-Four Month Extension Study of BA058-05-003 (Abaloparatide) in Participants With Osteoporosis

ACTIVExtend
Start date: November 20, 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to provide 24 months of standard of care data on participants previously enrolled in Study BA058-05-003 (NCT02653417).

NCT ID: NCT01656512 Completed - Osteoporosis Clinical Trials

Zometa Study in Pediatric Acute Lymphoblastic Leukemia

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

Acute Lymphoblastic Leukemia (ALL) is the most common malignancy in children. It accounts for one fourth of all childhood cancers & 74 % of childhood leukemia. Based upon drug registry data, children prescribed more than three courses of systemic glucocorticoids yearly faced a 20% increase in age-adjusted fracture rates. Rapid recovery occurred once glucocorticoids were discontinued, and fracture rates returned to expected for age by 1 year after treatment (Journal Of Clinical Endocrinology & Metabolism 2009). The investigators will study the role of bisphosphonates in the prevention of secondary osteoporosis in children & adolescents treated for ALL in the Children's Cancer Hospital -Egypt.

NCT ID: NCT01653275 Completed - Osteoporosis Clinical Trials

Mediterranean Diet for Post-menopausal Women: Effects on Bone Turnover

MedSD
Start date: April 2012
Phase: N/A
Study type: Interventional

The investigators propose a 24 week clinical research trial (12 week observational period followed by 12 week MedSD intervention) with feasibility of diet adoption and markers of bone turnover as the primary outcomes.

NCT ID: NCT01652690 Completed - Clinical trials for Osteoporosis, Postmenopausal

Prospective Observational Study to Describe Characteristics and Management of Patients Treated With Denosumab (Prolia®) in Routine Clinical Practice

Start date: June 26, 2012
Phase:
Study type: Observational

The objective of this prospective, observational study in Czech Republic and Slovakia is to describe per country the characteristics of women treated with denosumab in routine clinical practice and the clinical management of these patients during the first 2 years of treatment. In addition, the study aims to collect safety data in the real-life clinical practice settings on adverse drug reactions (ADRs) and serious ADRs.

NCT ID: NCT01633762 Completed - Obesity Clinical Trials

Eradication of Gut Microbiota

ERA
Start date: April 2012
Phase: Phase 0
Study type: Interventional

The aim of the study is to assess the effect of eradication of gut microbiota on 1) glucose metabolism including postprandial plasma responses of the incretin hormones GIP and GLP-1, insulin, C-peptide and glucagon, 2) metabolomic profiles and resting energy expenditure (REE) 3) appetite, satiety, food intake, gastric emptying and gall bladder emptying, 4) levels of markers of bone formation and resorption as well as serotonin, 5) markers of systemic inflammation, and 6) on the (prospective) composition of bacteria in faeces, blood and saliva. Thus, the overall objective is to provide detailed knowledge on the physiological role of gut microbiota combined with bioinformatic analyses of the functional implications of changes in bacteria composition on the level of both species and phylum.

NCT ID: NCT01633684 Completed - Diabetes Mellitus Clinical Trials

Type 1 Diabetes Mellitus Effect on Bone Mineral Density

Start date: August 2012
Phase: N/A
Study type: Observational

Because the diabetics are fracturing at a younger age than the general population (12), this leads us to believe there are significant factors that lead to fracture in Type 1 diabetes mellitus (DM) other than bone mineral density (BMD). Very little longitudinal data exists on BMD in adults with Type 1 DM and the effects of glucose control on BMD. No longitudinal data exists on pQCT in adults with Type 1 DM. Hypothesis: Adult subjects with diabetes and poor glucose control will lose bone mineral density (BMD) as measured by DXA compared to age and sex matched healthy controls.

NCT ID: NCT01631292 Completed - Osteoporosis Clinical Trials

Vitamin D Supplementation in Obesity and Weight Loss (3DD Study)

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

In this study, we will provide supplemental vitamin D in postmenopausal overweight/obese women, and hypothesize that it will not affect areal BMD, but will alter bone compartments (trabecular and cortical bone). In addition, higher vitamin D intake will increase serum 25OHD and suppress serum PTH and bone turnover during weight reduction. Secondary outcomes include the influence of vitamin D and weight loss on markers of insulin resistance and on cognitive tests of attention, learning, and memory.

NCT ID: NCT01631214 Completed - Clinical trials for Postmenopausal Women With Osteoporosis

Study to Determine the Efficacy and Safety of Romosozumab in the Treatment of Postmenopausal Women With Osteoporosis

ARCH
Start date: May 4, 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if treatment is effective in preventing fractures in women with postmenopausal osteoporosis.

NCT ID: NCT01627028 Completed - Osteoporosis Clinical Trials

Thai Traditional Massage Increases Biochemical Marker of Bone Formation in Postmenopausal Women

Start date: March 2011
Phase: Phase 3
Study type: Observational

To investigate the skeletal effect of Thai traditional massage by examining the changes in biochemical markers of bone turnover.

NCT ID: NCT01613144 Completed - Osteoporosis Clinical Trials

OsseoScrew Versus Fenestrated Pedicle Screws Augmented With Polymethylmethacrylate

EVOLVE
Start date: May 2012
Phase:
Study type: Observational

The purpose of this clinical investigation was to collect clinical evidence of the safety and efficacy of the OsseoScrew System. The OsseoScrew System is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion. The study was designed to compare the safety and efficacy of OsseoScrew compared to any other commercially available fenestrated pedicle screw system augmented with PMMA for posterior spinal fixation after surgical correction of spinal deformity or pathology.