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Osteoporosis clinical trials

View clinical trials related to Osteoporosis.

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NCT ID: NCT02435147 Completed - Osteoporosis Clinical Trials

Longitudinal Effects of Denosumab on Trabecular Bone Score and Femur Strength Index

Start date: April 2015
Phase:
Study type: Observational

The purpose of this study is to validate the long-term benefit of denosumab for osteoporosis treatment in a real-world clinical practice setting. We hypothesize that continued therapy (36+months) with denosumab will increase both trabecular bone score (TBS) and femur strength index (FSI) and reduce fracture and other bone health risks among post-menopausal women with osteoporosis.

NCT ID: NCT02429232 Not yet recruiting - Diabetes Mellitus Clinical Trials

A One-year Randomized Controlled Trial Evaluating the Impact of Pioglitazone Versus Linagliptin on Bone Turnover Markers

Start date: October 2015
Phase: Phase 4
Study type: Interventional

Diabetes mellitus is a common disease with much impact on human's health and is related to osteoporosis. But the mechanism remains unclear. The foreign researches revealed thiazolidinedione (TZD) would increase the risk of osteoporosis and bone fracture, specially elderly women. However, it is still controversial in terms of the youth and men. In Taiwan,there is few related study to analyze the relationship between TZD and steoporosis. This is a multicenter randomized controlled study.

NCT ID: NCT02422069 Completed - Clinical trials for Postmenopausal Osteoporosis

Study of Post Menopausal Osteoporosis (PMO) Among Gynecology Outpatients in Pakistan

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

This observational study will provide an opportunity to document local patterns of susceptibility, patient profile, and usefulness of screening in postmenopausal patients coming to gynecology outpatient clinics in Pakistan. This will also capture the initial management of PMO in diagnosed patients. The information gathered will serve as a foundation for developing national guidelines on screening and management of PMO in Pakistan.

NCT ID: NCT02421783 Completed - Clinical trials for Non-celiac Wheat Sensitivity

Osteoporosis In Non-Celiac Wheat Sensitivity Patients

Start date: May 1, 2015
Phase:
Study type: Observational

Non-celiac gluten sensitivity (NCGS) or 'wheat sensitivity' (NCWS) is included in the spectrum of gluten-related disorders. No data are available on the prevalence of low bone mass density (BMD) in NCWS. Our study aims to evaluate the prevalence of low BMD in NCWS patients and search for correlations with other clinical characteristics. This prospective observation study will include 90 NCWS patients with irritable bowel syndrome (IBS)-like symptoms, 90 IBS and 90 celiac controls. Patients will be recruited at the Internal Medicine and at the Gastroenterology Units of the University of Palermo. Elimination diet and double-blind placebo controlled (DBPC) wheat challenge proved the NCWS diagnosis. All subjects underwent BMD assessment by Dual Energy X-Ray Absorptiometry (DXA), duodenal histology, Human Leukocyte Antigen (HLA) DQ typing, body mass index (BMI) evaluation and assessment for daily calcium intake.

NCT ID: NCT02418273 Withdrawn - Osteoporosis Clinical Trials

Denosumab for Glucocorticoid-treated Children With Rheumatic Disorders

Start date: August 1, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate denosumab as a novel treatment for bone loss in children treated with glucocorticoids for rheumatic disorders. This is a pilot Phase 1/2, randomized open-label, 12-month clinical trial of denosumab to assess its effect on bone resorption markers and bone mineral density (BMD) in children with rheumatic disorders, age 4 to 16 years, recruited within 1 month of starting a chronic systemic glucocorticoid regimen. Primary outcomes include suppression of bone turnover markers and safety assessments. Secondary outcomes include changes in bone density as measured by dual energy X-ray absorptiometry (DXA) and peripheral quantitative computed tomography (pQCT) densitometry at the radius and tibia.

NCT ID: NCT02417389 Completed - Osteoporosis Clinical Trials

Efficacy of Cinacalcet in the Control of Primary Hyperparathyroidism

CA-PHP
Start date: May 2008
Phase: Phase 4
Study type: Interventional

To assess the efficacy and safety of treatment with cinacalcet and with cinacalcet plus alendronate in controlling bone loss induced by primary hyperparathyroidism.

NCT ID: NCT02416947 Completed - Clinical trials for Osteoporosis, Postmenopausal

Soluble Corn Fiber Effect on Bone Resorption in Post Menopausal Women

Start date: March 2012
Phase: N/A
Study type: Interventional

This study is designed to study the dose response effect of continuous Soluble Corn Fiber (SCF) intake over a 50 day period on bone resorption in healthy post menopausal women using the 41Calcium methodology. To further understand the dose response effect of SCF bone biomarkers will be studied. Our hypothesis is that soluble corn fiber will reduce bone resorption in a dose dependent manner in comparison to placebo when estimated by urinary 41Calcium excretion as well as bone biomarkers of resorption.

NCT ID: NCT02416271 Completed - Osteoporosis Clinical Trials

The Forteo Alendronate Comparator Trial

FACT
Start date: April 2001
Phase: Phase 4
Study type: Interventional

The main purpose of this study is to evaluate the effects of teriparatide with those of alendronate on spine bone mineral density (BMD) and other osteoporosis factors in postmenopausal women with osteoporosis.

NCT ID: NCT02399176 Completed - Osteoporosis Clinical Trials

Yoga in the Treatment of Osteoporosis

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

The study measures change in bone mineral density by the DEXA scan before and two or more years after beginning ten minutes of daily yoga designed to put pressure on the spine, hips and femur.

NCT ID: NCT02371252 Completed - Osteoporosis Clinical Trials

Efficacy and Safety of Brand Versus Generic Alendronate for Osteoporosis Treatment

Start date: April 2014
Phase: Phase 4
Study type: Interventional

Osteoporosis is a common disease defined as a decrease in bone mass and strength which increases risk of fragility fractures. This disorder may affecting health in many adults which causing disability, morbidity, and mortality. Current first-line medical therapy is bisphosphonates which alendronate is one of the most widely used. However, expenditure on medicines is one of the major problem of inadequate access to treatment. The investigators hypothesized that generic alendronate will have the same clinical efficacy as the brand formulation. Therefore, the result of this study is extremely crucial. If adequate efficacy of generic alendronate could be established and if it affords the same safety profile as those of brand alendronate, the use of generic alendronate could then be recommended.