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Bone Diseases clinical trials

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NCT ID: NCT05942690 Terminated - Osteopathia Clinical Trials

Osteopathic Intervention in Professional Handball Players

ECHODIAPOST
Start date: July 30, 2023
Phase: N/A
Study type: Interventional

The aim is to study the effectiveness of a common osteopathic intervention in professional handball players on diaphragmatic contractility and its correlations with posture. This study has never been done in healthy subjects. It is a scientific process of objectification of an osteopathic technique commonly performed in this population. The main objective is to assess diaphragmatic contractibility using ultrasound after abdominal osteopathic intervention (OMT).

NCT ID: NCT04271605 Terminated - Clinical trials for Osteoporosis, Postmenopausal

Intervention on Osteoporosis and Chronic Kidney Disease-mineral and Bone Disorder (CKD-MBD)

Start date: February 14, 2020
Phase: N/A
Study type: Interventional

Older adults having chronic kidney disease (CKD) have a higher rate of fracture than those without chronic kidney disease. Osteoporosis and chronic kidney disease mineral and bone disorder (CKD-MBD) are risk factors for skeletal fractures. In addition, CKD-MBD is also a risk factor for cardiovascular disease. Pharmacological and non-pharmacological therapy are both important to prevent complications of chronic kidney disease and osteoporosis. Therefore, a prospective intervention study is purposed to investigate the effect of a multifaceted intervention including exercise, diet modification, and pharmacological therapy on their outcomes. Patients who are older than 50 years old and have chronic kidney disease G3-G4 (estimated glomerular filtration rate > 20 ml/min per 1.73 m2) with a high risk of fracture (screening by Fracture Risk Assessment Tool (FRAX®)) are enrolled. Baseline questionnaire, clinical, laboratory and radiological examination are performed. If CKD-MBD or osteoporosis are revealed, the intervention will be given accordingly. All examinations will be repeated every 3 months, except bone mineral density and x-ray film for the spine to investigate the effect of the intervention. After one-year, primary outcomes including mortality, cardiovascular events, subsequent fracture, and fall rate will be examined. The secondary outcomes include changes in biochemistry laboratory data before and after interventions (pharmacological therapy and lifestyle modifications). The bivariate analysis will be performed using the t-test or Mann-Whitney U test for continuous variables with normal or non-normal distribution, respectively. Chi-squared test for categorical variables will be used to test correlations between baseline characteristics, change of laboratory results and outcomes. The paired t-test will be used to examine the difference between before and after the interventions. Stepwise multivariate logistic regression models will be used to identify the correlates of outcomes after adjusting for potential confounders.

NCT ID: NCT03802656 Terminated - Scoliosis Clinical Trials

Vertebral Body Tethering Treatment for Idiopathic Scoliosis

Start date: June 24, 2019
Phase: N/A
Study type: Interventional

This study will determine whether vertebral body tethering is a safe and feasible method of treatment for pediatric idiopathic scoliosis.

NCT ID: NCT02070484 Terminated - Clinical trials for Musculoskeletal Diseases

Human Amniotic Tissue-derived Allograft, NuCel, in Posteriolateral Lumbar Fusions for Degenerative Disc Disease

Start date: February 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effect and safety of NuCel to DBX on patients undergoing posteriolateral lumbar spinal fusions for degenerative disc disease.

NCT ID: NCT01725113 Terminated - Kidney Failure Clinical Trials

Management of Mineral and Bone Disease in Hemodialysis-Calcitriol vs. Paricalcitol

ECRIP
Start date: November 2012
Phase: Phase 4
Study type: Interventional

The purpose of this non-inferiority study is to compare the safety and effectiveness of a mineral and bone disease treatment protocol based on calcitriol to one based on paricalcitol in hemodialysis patients using revised Kidney Disease: Improving Global Outcomes (KDIGO) parathyroid hormone targets.

NCT ID: NCT00904423 Terminated - Breast Cancer Clinical Trials

Ph I/II of Vitamin D on Bone Mineral Density & Markers of Bone Resorption

Start date: April 2009
Phase: Phase 1/Phase 2
Study type: Interventional

Aromatase inhibitors are potent suppressors of breast cancer growth, but side effects include bone loss, fractures, arthralgias and myalgias. We hypothesize vitamin D administration might be beneficial in treating these symptoms and to protect bone.

NCT ID: NCT00711763 Terminated - Preterm Infants Clinical Trials

Calciuric Effect and Cyclic Parenteral Nutrition in Preterm Infants

Start date: July 2008
Phase:
Study type: Observational

The aim of our work is to study the effect of total parenteral nutrition (TPN) cycling in preterm infants on hypercalcuria (excessive calcium excretion in urine). TPN cycling refers to administering the TPN over a portion of the day rather than the whole day. Our hypothesis is that cyclic TPN includes more hypercalcuria in preterm infants as compared to continuous TPN. Objectives: Measure Urinary Calcium(Ca) during the periods of continuous and cyclic TPN. Compare the amount of Ca losses in the urine continuous vs. cyclic TPN

NCT ID: NCT00698347 Terminated - Clinical trials for Rheumatoid Arthritis

A Clinical Investigation of the M2a-Magnumâ„¢ Hip System

Start date: November 2004
Phase: N/A
Study type: Observational

The purpose of this prospective clinical data collection is to document the performance and clinical outcomes of the M2a-Magnumâ„¢ Hip System

NCT ID: NCT00663104 Terminated - Coronary Disease Clinical Trials

Effect of Exercise and Phytoestrogen on Bone, Metabolic Syndrome Criteria and Complaints of the Early Menopause

Start date: April 2008
Phase: Phase 3
Study type: Interventional

The aim of the study is to compare the effect of a progressive, periodized exercise training designed to impact bone, CHD-risk-factors and menopausal complaints versus the combined effect of exercise and "phytoestrogen" (cimicifuga racemosa; CR). After randomization, 84 females 1-3 year postmenopausal with no medication or illness affecting bone metabolism exercise over 12 months (EG; 42 with, 42 without CR), 42 women serve as wellness-control. Three group training sessions/week will be performed in the EG. Both groups will be individually supplemented with calcium and Vit-D (cholecalciferol).

NCT ID: NCT00591162 Terminated - Burn Clinical Trials

Bone Disease in Severely Burned Children

Start date: October 1992
Phase: Phase 2/Phase 3
Study type: Interventional

Bone metabolism is adversely affected by severe burns in children for a period of time.