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Bone Diseases clinical trials

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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: NCT01150071 Completed - Clinical trials for Lung Diseases, Obstructive

Growth, Health and Development in Children Born Extremely Preterm

PEP11
Start date: August 2010
Phase: N/A
Study type: Observational

Background: In a national Norwegian cohort of children born before 28 weeks gestation or with a birth weight less than 1000 g born in 1999 and 2000, 372 survived. Compared with earlier studies survival increased for the most immature infants, but at the cost of more early complications and a high rate of impairments, while the less immature children had fewer early complications and less impairments detectable within 5 years. These changes show the importance of monitoring outcome as treatment modalities change. Large brain haemorrhages were highly predictive of severe disabilities, but we have not found good predictive factors for milder impairments such as cognitive, behavioural and motor difficulties. However, at 5 years later function may be difficult to predict, and the children's potentials are better understood after completing several years in school. Objectives: The children will be re-examined at age 11 in order to assess their physical and mental health, and cognitive, motor and social function, and to determine if early life events and development at 2 and 5 years are predictive of long term health and functioning. MRI-studies, including functional MRI will be performed to examine if different outcomes related to brain function can be explained by differences in brain development. Methods: For all, data will be collected from the compulsory national test in 5th grade and questionnaires to the child, parents and teacher. For children in Western Norway (n=87) extensive examinations of lung and brain function, including clinical diagnostic tests and MRI, will be added. For all aspects of the study the investigators have appropriate current and historic reference populations for comparison. Implications: Knowledge on causes and of early predictions of outcome is needed to give appropriate advice to families, professionals and society, and to develop preventive programs.

NCT ID: NCT01108211 Completed - Scoliosis Clinical Trials

Improving Low Bone Mass With Vibration Therapy in Adolescent Idiopathic Scoliosis (AIS)

Start date: January 2009
Phase: Phase 3
Study type: Interventional

This is a prospective randomized controlled trial investigating the effect of vibration therapy on bone mineral density (BMD) and bone quality in AIS subjects suffering from osteopenia (low bone mass).

NCT ID: NCT01067508 Completed - Clinical trials for Bone Diseases, Metabolic

Effects of Naturally Silicon-Rich Water on Bone Metabolism in Women

Start date: June 2007
Phase: N/A
Study type: Interventional

The aim of this research study is to determine by laboratory analyses the effects of drinking silicon-rich water on bone health. This will be determined from blood and urine samples from subjects who will be asked to drink 1 liter per day of either silicon-rich water or water without silicon for 12 weeks.

NCT ID: NCT01041456 Completed - Clinical trials for Protein Malnutrition

Laparoscopic Revision From Biliopancreatic Diversion to Gastric Bypass

BPD-to-RYGB
Start date: March 2009
Phase: N/A
Study type: Observational

The aim of this study is to describe the clinical presentation, indications, and operative treatment as well as assess the morbidity, mortality, and overall performance of revisional GBP after either failed and/or complicated Biliopancreatic Diversion "BPD" for weight loss. With such information, we hope to determine what features might assist us in advancing our knowledge about mechanisms of failure after primary bariatric surgery, mechanism of action of revisional GBP, and performance of revisional GBP through traditional outcome measurements as well as identifying predictors of good or poor outcome after revisional GBP in this specific subpopulation.

NCT ID: NCT01002872 Completed - Clinical trials for Metabolic Bone Disease

The Effect of Lanthanum Carbonate on Fibroblast Growth Factor 23 ( FGF23) in Chronic Kidney Disease

Start date: October 2009
Phase: N/A
Study type: Interventional

The aim of the study is to assess the effects of the drug lanthanum carbonate (a phosphorus binder drug) on c-terminal and on FGF23 levels in patients with Chronic Kidney Disease (CKD). Targeting FGF23 measurement in CKD patients may impact both the progression of kidney disease and patient mortality.

NCT ID: NCT00995163 Completed - Clinical trials for End Stage Renal Disease

Mineral and Bone Disorders Outcomes in Stage 5D of Chronic Kidney Disease

MBD-5D
Start date: January 2008
Phase: N/A
Study type: Observational

The MBD-5D is a prospective observational study with a case-cohort and a cohort design. Eligible patients are receiving hemodialysis and have secondary hyperparathyroidism. The study's three goals are (1) to record the patients' characteristics, and variation in the patterns of their treatment; (2) to analyze factors associated with variation in those medical practice patterns; and (3) to identify practice patterns and other factors that affect hospitalization, mortality, and other patient-level outcomes.

NCT ID: NCT00965978 Completed - Osteoporosis Clinical Trials

A Study to Evaluate Food Effect on ONO-5920/YM529 Intermittent Formulation

Start date: July 2009
Phase: Phase 1
Study type: Interventional

The aim of the study is to evaluate the effects of food intake on the plasma concentration profile of YNO-5920/YM529 in post menopausal women.

NCT ID: NCT00935935 Completed - HIV Infections Clinical Trials

Study of Bone Disease in Older HIV-infected Adults

Start date: December 2009
Phase: N/A
Study type: Observational

This study will look to see if there are changes in the blood cells that are associated with bone disease and sort out effects that are due to the HIV virus itself, the medications and see if faster aging occurs in the cells of HIV infected persons. Bone disease will be measured by a special X-ray called a DEXA scan. A DEXA scan is used by doctors to see if someone has normal bone mass for their age or if there is thinning of the bones. The purposes of this study are: - to learn how common bone disease is in HIV infected patients over the age of 50 years that receive their care at the CORE Center - to see what are the common causes of bone disease in older HIV infected persons - to see if there are differences in blood cells and levels of cytokines in patients who do or do not have bone disease, as this may help researchers determine the cause of bone disease.

NCT ID: NCT00913796 Completed - Metabolic Acidosis Clinical Trials

Metabolic Acidosis in Renal Transplant Patients

MART
Start date: December 2007
Phase: Phase 2
Study type: Interventional

Acidosis (accumulation of acid in the body) may be an underrecognized problem in patients after renal transplantation. It may have consequences on physical performance due to negative effects on bone and muscle metabolism. Therefore, the purpose of this study is 1. to determine the status of physical capacity and bone structure in renal transplant patients with metabolic acidosis 2. to study the effect of substituting base equivalents (citrate) on acid/base status of renal transplant patients with acidosis 3. to compare the status of physical capacity and bone structure in renal transplant patients with metabolic acidosis before and after substitution with citrate