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Bone Loss, Age-Related clinical trials

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NCT ID: NCT04265742 Completed - Clinical trials for Bone Loss, Age-related

Microbiota and Bone Fragility:Study of the Relation Between Gut Microbiota and Bone Microarchitecture

MICROBONE
Start date: February 8, 2019
Phase: N/A
Study type: Interventional

Gut microbiota regulate metabolism of their human host. Some diseases are associated with variations in gut microbiota diversity and higher fracture risk. Intestinal bacteria synthesize or influence synthesis of factors modulating bone metabolism. The link between gut microbiota and bone was assessed mainly in experimental animal studies. Clinical data, e.g. on the role of gut microbiota in postmenopausal osteoporosis are scarce. The investigators will compare gut microbiota composition in four groups of women aged ≥60 recruited on the basis of bone mineral density (BMD) and personal history of fracture. the participants will have diagnostic exams: clinical tests, bone densitometry (body composition, vertebral fractures), high resolution peripheral QCT (bone strength estimated by microfinite element analysis, micro-FEA), biological sample collection. Gut microbiome profiling will be performed at the INRA MetaGenoPolis laboratory. The investigators will compare gut microbiota diversity according to BMD level and to the fracture status. The investigators will analyze interactions of the gut microbiota diversity with bone status (bone turnover rate, BMD, bone microarchitecture, bone strength estimated by micro-FEA), muscle mass and strength, inflammatory cytokines and micro-RNAs modulating their expression. This study will provide new data concerning the importance of gut microbiota for the fracture risk in older women. It will help to identify the main metabolic pathways underlying the observed associations.

NCT ID: NCT02751008 Completed - Clinical trials for Bone Loss, Age-Related

Bone Fragility Study in Pediatric Population With Risk Factors

Start date: April 2016
Phase:
Study type: Observational

Low bone mass and osteoporosis are underdiagnosed in childhood in our environment and its prevalence is unknown. In most cases they are secondary to chronic diseases that conduct to a poor bone health condition and thereby a risk of fracture increased. The aim of this study is to identify patients with risk factors for low bone mass and determine their Bone Mineral Density (amount of bone) by performing bone densitometry and compared with healthy population of the same characteristics. Also the investigators want to evaluate bone quality by application of Trabecular Bone Score to images obtained by densitometry. As secondary objectives the investigators intend to correlate the data with with clinical variables to identify the most important in bone health clinical factors. In addition to measuring bone quality and quantity demographic and clinical process related to bone quality base and variables will be collected.

NCT ID: NCT02349113 Completed - Clinical trials for Bone Loss, Age-related

Effects of Acute Estrogen Therapy on Bone Formation

Start date: February 2012
Phase: Phase 1
Study type: Interventional

This study is being done to study age-related bone changes in women. The investigators know that the major cause of osteoporosis is a shortage of the female hormone estrogen. This study will look closer at how this shortage of estrogen works to cause a decrease in bone formation.

NCT ID: NCT00794443 Completed - Osteoporosis Clinical Trials

ONO-5920/YM529 Confirmatory Study in Involutional Osteoporosis Patients

Start date: November 2008
Phase: Phase 2/Phase 3
Study type: Interventional

This is a multi-center double-blind parallel-group study in involutional osteoporosis patients to compare the efficacy and safety of monthly oral intermittent formulation ONO-5920/YM529 with its daily formulation.

NCT ID: NCT00578981 Completed - Osteoporosis Clinical Trials

Osteoporosis Choice Decision Aid for Use of Bisphosphonates in Postmenopausal Women

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

To develop a decision aid to support the decision to use (or not use) bisphosphonates in postmenopausal women at risk for osteoporotic fractures, and to assess the impact of the decision aid on start and six month adherence to bisphosphonates.