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Bone Diseases, Metabolic clinical trials

View clinical trials related to Bone Diseases, Metabolic.

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NCT ID: NCT03084432 Completed - Clinical trials for Apnea of Prematurity

Effect of Caffeine on Preterm Infants' Bone Mineral Content

Start date: December 1, 2014
Phase: N/A
Study type: Observational

The primary objective was to determine whether caffeine therapy is associated with decreases bone mineral content using dual energy x-ray absorptiometry. Secondary objectives were to determine whether caffeine therapy is associated with increased incidence of nephrocalcinosis or bone fracture.

NCT ID: NCT03026660 Completed - Clinical trials for Postmenopausal Osteoporosis

Moringa Oleifera on Bone Density

Start date: July 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effects of Moringa Oleifera on the structure and function of bone in post-menopausal women ingesting 1000 mg of Moringa Oleifera daily for 12 weeks.

NCT ID: NCT02999204 Completed - Clinical trials for Renal Insufficiency, Chronic

Effect of Vitamin D3 Supplementation on Arterial and Bone Remodeling in Chronic Kidney Disease Patients

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

To evaluate in patients with chronic kidney disease the impact of two dosages of per os vitamin D3 supplementation (cholecalciferol) on large arterial stiffness (evaluated non invasively by pulse wave velocity and high-resolution echotracking system). We will also study arterial calcification (lateral abdominal radiography and echocardiogram), arterial remodeling (high-resolution echotracking system), endothelial function (evaluated by a non-invasive finger biosensor device), and bone remodeling (evaluated by serum biomarkers and bone mineral density).

NCT ID: NCT02853539 Completed - Clinical trials for Metabolic Bone Disease

Denosumab in Metabolic Bone Disease in Chronic Intestinal Failure Patients

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

Low bone mineral density (BMD) is commonly reported in patients receiving home parenteral nutrition (HPN). Denosumab represent a new drug, which helped to prevent osteoclast. The aim of the study was to assess its value in chronic intestinal failure patients.

NCT ID: NCT02785744 Completed - Gaucher Disease Clinical Trials

Genzyme Osteopenia/Osteoporosis Study

Start date: April 1, 2016
Phase:
Study type: Observational

Gaucher disease is a most common genetic metabolic disease characterized by low platelet number, liver and spleen enlargement and various forms of bone diseases including low bone mineral density leading to brittle bones. Various treatment options are now available for this disease. The purpose of this research study is to determine the prevalence of Gaucher disease in patients with low bone mineral density as observed by DEXA scan, which is a form of X-Ray of the bone.

NCT ID: NCT02763280 Completed - Osteopenia Clinical Trials

Efficacy and Safety of Ginseng Extract on Improvement of Bone Metabolism in Menopausal Women

Start date: June 2015
Phase: N/A
Study type: Interventional

Recently, osteoporosis has been recognized as a serious health problem in the elderly, it has also increased in young • middle-aged layer. Ginseng is history 2, 000 years Korean typical herbal medicine which is used as a medicinal is known the mystery of Elixir from a long time ago. A previous study was administered ginseng extract results in animal models induced osteoporosis, the bone-related biomarkers, including improved bone density and bone mass.

NCT ID: NCT02731820 Completed - Osteopenia Clinical Trials

Efficacy of Potassium Citrate in the Treatment of Postmenopausal Osteopenia

ACAROS
Start date: September 1, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate whether the use of alkali compounds, i.e. potassium citrate (K3C6H5O7, hereinafter KCitr) is effective in preventing the progression of osteopenia. A randomized clinical trial (RCT, placebo-controlled, double-blind) has been planned to evaluate the effect of the daily administration of KCitr (3 g/die, K 30 mEq). The efficacy will be evaluated by comparing the circulating levels of bone turnover markers at the baseline and after the treatment (3, 6 months).

NCT ID: NCT02722980 Completed - Osteopenia Clinical Trials

Efficacy of a Probiotic Product on Bone Mineral Density (BMD) in Healthy Women in Early Post-menopausal Phase

ProBone16
Start date: April 2016
Phase: N/A
Study type: Interventional

The aim of the current study is to evaluate the efficacy of a probiotic product on bone mineral density (BMD) in healthy early post-menopausal women, compared to placebo. The primary endpoint is to assess changes of BMD at lumbar spine after an intervention period of 12 months. Changes in BMD at the femoral neck (hip) will also be measured as well as changes in bone turnover markers during the period of 12 months.

NCT ID: NCT02604836 Completed - Clinical trials for Postmenopausal Osteoporosis

A Study of Ibandronate (Boniva) to Evaluate Satisfaction in Women With Post-Menopausal Osteoporosis or Osteopenia

Start date: June 2004
Phase: Phase 4
Study type: Interventional

This study will investigate participant satisfaction (including compliance, preference, tolerability) with once-monthly Bonviva in women with post-menopausal osteoporosis or osteopenia transitioned from once-weekly alendronate or risedronate. The anticipated time on study treatment is 6 months, and the target sample size is 1776 individuals.

NCT ID: NCT02598453 Completed - Clinical trials for Postmenopausal Osteoporosis

PRIOR Study - A Study of Ibandronate (Boniva) in Postmenopausal Women With Osteoporosis or Osteopenia

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

The purpose of this study is to evaluate treatment adherence to different regimens of ibandronate in postmenopausal women with osteoporosis or osteopenia who are intolerant to daily or weekly alendronate or risedronate therapy due to gastrointestinal (GI) side effects. The anticipated time on study treatment is 12 months, and the target sample size is 517 individuals.