Osteoporosis Fracture

4

Review clinical trials related to Osteoporosis Fracture. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Peripheral Mononuclear Cells to Screen, Monitor and Stratify the Population at Risk of Osteoporosis and Fractures

Osteoporosis (OP) is one of most common age-associated and chronic metabolic bone diseases, featured by a decrease of bone mineral density (BMD) that increases the risk of bone fractures.OP guidelines agree that Dual-X-ray Absorptiometry (DXA) is the gold standard for BMD assessment, but for the different OP stages screening and diagnosis, BMD by itself is not an accurate predictor. Thus, OP is often misdiagnosed. Aim of the this study is to improve a tool for OP diagnosis based on the ability of circulating peripheral blood mononuclear cells (PBMCs) to maintain or not their in vitro viability (IRCCS Istituto Ortopedico Rizzoli European patent n.3008470 March 21, 2018) for the measurement of the different OP severity levels, also considering specific gender related differences.

Participants needed: 120
Trial details
Age: 40+Biological sex: AllType: ObservationalSponsor: Istituto Ortopedico RizzoliUpdated: May 28, 2026Locations: 2
Eligibility criteria

Healthy patients (at risk and undergoing periodic follow-up and/or attending out... [+4]

Hematopoietic system disorders (hemolytic, aplastic, and neoplastic anemias) [+8]

Status: Not yet recruiting

The Effect of Semaglutide on Bone Health

Semaglutide has effects that include lowering blood sugar, reducing weight, and improving cardiovascular and renal outcomes, and it is now widely used in clinical practice. Given that weight loss is associated with bone loss, its effect on bone health has recently raised concerns. Therefore, the goal of this clinical trial is to learn the effect of semaglutide on bone mineral density and fractures in patients with type 2 diabetes. The investigators will compare semaglutide combined with metformin to metformin alone to see if semaglutide treatment has effects on bone mineral density and bone turnover markers in patients with type 2 diabetes after 12 months. The intervention group will receive semaglutide combined with metformin for 12 months, while the control group will receive metformin alone for the same duration. After 12 months of treatment, the investigators will compare the bone mineral density, fracture incidence, and levels of bone turnover markers between the two groups.

Participants needed: 150
Trial details
Phase: Phase 4Age: 50-75Biological sex: AllType: InterventionalSponsor: The First Affiliated Hospital of Xiamen UniversityUpdated: Sep 17, 2025Locations: 1
Eligibility criteria

Type 2 diabetes (according to WHO diagnostic criteria), [+4]

Bone mineral density (lumbar spine, hip, or femoral neck) T-score < -2.5, [+6]

Status: Recruiting

New Biomarkers and Therapeutic Targets in Osteoporosis Via Omics Technologies

This study aims to discover novel biomarkers and therapeutic targets for osteoporosis through the use of advanced omics technologies, including proteomics and metabolomics. By analyzing bone and plasma samples from patients with osteoporosis, the research seeks to understand the underlying mechanisms of the disease and identify potential diagnostic and therapeutic biomarkers.

Participants needed: 60
Trial details
Biological sex: FemaleType: ObservationalSponsor: National and Kapodistrian University of AthensUpdated: Jul 29, 2024Locations: 1
Eligibility criteria

Postmenopausal Female Patients with osteoporotic subcapital femoral neck fractur... [+1]

Patients that have undergone before osteoporotic fractures [+1]

Status: Recruiting

Development and Validation of a Postoperative Re-fracture Risk Model for Osteoporotic Spinal Fractures

In this project, IDEAL-IQ technology and PDFF and R2\* image-based imaging methods are used to analyze the intrinsic relationship between preoperative vertebral bone marrow fat content, magnetic susceptibility properties of bone tissue and bone strength (bone volume and bone mass), to explore the mechanism of vertebral re-fracture after PVP / PKP, and to explore the imaging markers for the risk of postoperative vertebral re-fracture after PVP / PKP. To construct a precise and individualized risk assessment model of vertebral re-fracture after PVP/ PKP by combining clinical risk factors, preoperative quantitative MRI parameters (PDFF, R2\*) and imaging characteristics, so as to achieve the goal of objectively and accurately evaluating the risk of vertebral re-fracture at the early stage of the postoperative period (1 year).

Participants needed: 560
Trial details
Age: 50-90Biological sex: AllType: InterventionalSponsor: The Seventh Affiliated Hospital of Sun Yat-sen UniversityUpdated: Apr 23, 2024Locations: 1
Eligibility criteria

Patients diagnosed with osteoporotic vertebral fractures of the thoracic and lum... [+2]

History of severe scoliosis, vertebroplasty, or internal spinal fixation; [+2]