Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to Osteoporosis from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 17
- Active, not recruiting: 9
- Completed: 13
- Other: 11
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT00024804 — A Natural History Study of Bone and Mineral Disorders
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Dental and Craniofacial Research (NIDCR) |
| Enrollment | 1000 |
| Study Type | OBSERVATIONAL |
| Conditions | Tumor Induced Osteomalcia; Osteomalacia; Familial Tumoral Calcinosis |
This study has four objectives: 1) to provide investigators the opportunity to study bone specimens from patients with various skeletal diseases; 2) to treat patients with skeletal diseases at the NIH; 3) to expose NIH trainees to certain skeletal diseases; and 4) to gain more knowledge about skeletal diseases and stimulate further study of bone biology.
Anyone with a disease that affects the …
NCT07665424 — Safety and Efficacy Clinical Trial of the Vessel-X® Bone Filling Container System
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Juin-Hong Cherng |
| Enrollment | 146 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoporosis; Osteoporotic Vertebral Compression Fractures |
| Interventions | ; |
Osteoporotic vertebral compression fractures (OVCFs) are a common and serious complication of osteoporosis, particularly among elderly and postmenopausal patients. OVCFs may result in severe pain, functional impairment, spinal deformity, and reduced quality of life. Conventional conservative treatments, including bed rest, analgesics, and bracing, may provide limited symptom relief. Minimally i…
NCT05266976 — Mode of Exercise and Bone Biomarkers in Older Veterans
| Status | Recruiting |
| Phase | N/A |
| Sponsor | VA Office of Research and Development |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Aging; Musculoskeletal Diseases; Osteoporosis |
| Interventions | ; |
Adults are often encouraged to exercise to maintain or improve bone health. However, there is evidence that exercise does not always lead to increases in bone mass, and exercise could lead to bone loss under certain conditions. Endurance exercise can increase bone resorption following an exercise bout, which may explain why bone does not always favorably adapt to exercise, but it is unclear if …
NCT05764733 — Bone, Exercise, Alendronate, and Caloric Restriction
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Wake Forest University Health Sciences |
| Enrollment | 900 |
| Study Type | INTERVENTIONAL |
| Conditions | Bone Loss |
| Interventions | ; ; |
The purpose of this research is to identify strategies that minimize bone loss that occurs when older adults lose weight. Participation in this research will involve up to nine assessment visits and last up to two years.
NCT06059222 — The Optimised Use of Romozosumab Study
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | University of Aarhus |
| Enrollment | 270 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoporosis |
| Interventions | ; ; |
OPTIMIST is a two-year, randomised, active controlled, open-label, multicentre intervention trial. OPTIMIST includes 3 treatment groups each comprising combinations of romosozumab (ROMO) and zoledronate (ZOL) treatment used in standard doses (210 mg monthly (sc) and 5 mg yearly (iv), respectively).
The study will investigate if it is possible to maximize the effect of romosozumab by giving it …
NCT06551155 — Peripheral Mononuclear Cells to Screen, Monitor and Stratify the Population at Risk of Osteoporosis and Fractures
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Istituto Ortopedico Rizzoli |
| Enrollment | 120 |
| Study Type | OBSERVATIONAL |
| Conditions | Osteoporosis; Osteopenia; Osteoporosis Fracture |
| Interventions |
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…
NCT06938152 — Effects of Cycle Therapy vs Sequential Therapy With Romosozumab and Denosumab in Postmenopausal Osteoporosis Patients
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | National Taiwan University Hospital |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoporosis; Osteoporosis Postmenopausal |
| Interventions | ; |
This study is a prospective, randomized, controlled clinical trial comparing the efficacy of a 24-month cyclic therapy regimen (6 months of Romosozumab followed by 6 months of Denosumab, repeated for two years) versus a traditional sequential treatment regimen (12 months of Romosozumab followed by 12 months of Denosumab). The goal is to determine which approach yields better therapeutic outcome…
NCT07616401 — MicroRNA and Markers and Therapeutic Response to Romosozumab and Abaloparatide in Postmenopausal Osteoporosis
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Istituto Auxologico Italiano |
| Enrollment | 42 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoporosis; Menopause |
| Interventions |
Osteoporosis is a systemic skeletal disorder affecting approximately 10% of individuals over 50 years of age. It is characterised by an increased risk of fragility fractures, which constitute a major source of morbidity, mortality, and healthcare burden worldwide.
A range of pharmacological therapies has been approved for osteoporosis, with demonstrated efficacy in reducing fracture risk. Thes…
NCT07154719 — GLP-1R Actions on Muscle and the Skeleton
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Pennington Biomedical Research Center |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Musculoskeletal Abnormalities; Obesity; Sarcopenic Obesity; Osteoporosis; Drug Effect |
| Interventions | ; |
The GRAMS study objectives are to assess the musculoskeletal changes that occur after weight loss using GLP-1 based therapy. A lifestyle intervention with diet and exercise is included to assess any mitigating effects are provided, versus a control group with regular exercise and diet.
NCT07143669 — Screening Study for KIT D816V Mutated Mast Cell Disease in Select Populations
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Blueprint Medicines Corporation |
| Enrollment | 450 |
| Study Type | OBSERVATIONAL |
| Conditions | Clonal Mast Cell Disease; KIT D816V Mutation; Suspected KITD816V Mutated Clonal Mast Cell Disease |
| Interventions |
This is a multicenter screening study to characterize the prevalence of the KIT D816V mutation in participants with suspected clonal mast cell disease.
NCT07301749 — A Clinical Study Evaluating the Safety and Efficacy of the VCFix Spinal System for Treatment of Vertebral Compression Fractures
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Amber Implants B.V. |
| Enrollment | 148 |
| Study Type | INTERVENTIONAL |
| Conditions | Vertebral Compression Fracture |
| Interventions |
This study is being conducted to evaluate the safety and performance of the VCFix Spinal System, a medical device designed to treat certain types of spinal fractures called vertebral compression fractures (VCFs) in adults.
Up to 8 hospitals in Europe will take part in the study. All participants will receive treatment with the VCFix device. The treatment will be provided according to the inten…
NCT07651306 — Radiographic Cortical Thickness of the Humerus in Detecting Post-Stroke Regional Bone Loss
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Istanbul Physical Medicine Rehabilitation Training and Research Hospital |
| Enrollment | 65 |
| Study Type | OBSERVATIONAL |
| Conditions | Hemiparesis After Stroke; Dual Energy X-ray Absorptiometry; Osteoporosis |
Post-stroke immobilization and reduced weight-bearing frequently lead to significant regional bone mineral density loss and asymmetry, particularly in the paretic upper extremity, which increases fracture risks. While Dual-Energy X-ray Absorptiometry (DXA) is the gold standard for evaluating systemic bone loss, it primarily focuses on axial or lower extremity sites and lacks universal accessibi…
NCT07620834 — Artificial Intelligence-Guided Diagnosis for High-Risk Osteoporosis Populations: A Pragmatic Randomized Clinical Trial
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Taichung Veterans General Hospital |
| Enrollment | 1180 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoporosis |
| Interventions |
Project Summary
I. Project Objectives
With the rapid advancement of medical technology, smart medical devices have become one of the key components of modern healthcare. However, integrating these emerging technologies into the national health insurance (NHI) reimbursement system while ensuring their clinical value and economic benefits remains a major challenge worldwide.
The primary goal o…
NCT07325578 — U.S. Prospective Evaluation of EPIONE Device for Percutaneous MSK Procedures
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Precision IO Group |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Bone Tumor; Osteoporosis; Traumatic Fracture |
| Interventions |
The goal of this investigational device exemption is to evaluate the Epione assistance for introducer placement during percutaneous procedures in musculo-skeletic (MSK) structures of the pelvis and the spine in adults.
The main question is the determination of the rate of feasible procedures assisted by the Epione device
Participants will undergo their procedure(s) as planned by their physici…
NCT07677033 — Functional Muscle-Bone Incongruity Index (FKUI): A Prospective Observational Study
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Kanuni Sultan Suleyman Training and Research Hospital |
| Enrollment | 200 |
| Study Type | OBSERVATIONAL |
| Conditions | Osteoporosis; Musculoskeletal Health; Sarcopenia; Osteopenia |
The Functional Muscle-Bone Incongruity Index (FKUI) is a novel approach developed to evaluate the relationship between muscle function and bone health. This prospective observational study aims to investigate the clinical applicability of FKUI, which combines handgrip strength, total hip bone mineral density (BMD), and lumbar-hip BMD discordance. Approximately 200 adult participants undergoing …
NCT07621679 — People With Osteoporosis Can Walk-BEST to Reduce Fall and Fracture Risk
| Status | Recruiting |
| Phase | N/A |
| Sponsor | McGill University Health Centre/Research Institute of the McGill University Health Centre |
| Enrollment | 28 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoporosis |
| Interventions | ; |
The aim of the Walk BEST study is to provide evidence that it is feasible to implement the technology assisted gait- focused walking program Walk-BEST™ in older adults with osteoporosis, and that this program is acceptable to this population.
NCT07677072 — Can Serum Lumican Level Identify a Hidden Fragility Phenotype Beyond Bone Mineral Density in Postmenopausal Women?
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Kanuni Sultan Suleyman Training and Research Hospital |
| Enrollment | 98 |
| Study Type | OBSERVATIONAL |
| Conditions | Osteoporosis; Postmenopausal Osteoporosis; Frailty; Fragility Fractures |
Osteoporosis is a major cause of morbidity and fragility fractures in postmenopausal women. Bone mineral density (BMD) alone may not fully reflect fracture risk and skeletal fragility. Lumican, an extracellular matrix proteoglycan involved in collagen organization and musculoskeletal tissue homeostasis, has emerged as a potential biomarker for bone health. This prospective observational study a…
Active, Not Recruiting
NCT02194660 — Fragility Fracture Liaison Service Project
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | National Taiwan University Hospital |
| Enrollment | 600 |
| Study Type | OBSERVATIONAL |
| Conditions | Osteoporosis; Fracture |
Aims: to Establish the FLS services at the National Taiwan University Hospital (NTUH) and its Beihu Branch (BB).
Method: From Jan., 2014, two related fracture liaison services (FLSs) following the 13 ‘Capture the Fracture Best Practice Standards’ were implemented at the National Taiwan University Hospital (NTUH) health care system. The main hospital (MH) program enrolled patient with 1) new hi…
NCT02194647 — Anti-osteoporosis Medication Monitoring and Management Service
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | National Taiwan University Hospital |
| Enrollment | 500 |
| Study Type | OBSERVATIONAL |
| Conditions | Osteoporosis; Fracture |
BACKGROUND:
One-year adherence to oral anti-osteoporosis medication (AOMs) was only about 30%. In recent years, efforts have been made to change the delivery of these medications from oral form to injection form every, 3, 6 or 12 months to increase adherence. However, both patients and providers are sometimes confused about the multiple choices. Also, patients may receive extra medications if …
NCT02822378 — Dried Plums and Bone Health in Postmenopausal Women
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Penn State University |
| Enrollment | 322 |
| Study Type | INTERVENTIONAL |
| Conditions | Postmenopausal Osteoporosis |
| Interventions | ; ; |
Postmenopausal women often seek non-pharmacologic interventions for the protection of bone health. Previous research in humans and rodents has indicated that dietary dried plum consumption may be beneficial for bone health, especially in postmenopausal women. However, it is unknown in what quantity dried plums need to be consumed to be of benefit and through what mechanisms dried plums act to i…
NCT07669181 — Examination of the Role of Human Exoskeletons in Rehabilitation
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University of Pecs |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Spinal Cord Injury |
| Interventions |
Background and Rationale:
Traumatic spinal cord injury (SCI) affects approximately 12,400 individuals annually in the USA, predominantly impacting healthy young adults aged 20-40 years. Complete SCI above the lumbar region results in paraplegia or tetraplegia, severely compromising quality of life. Wheelchair-dependent lifestyle and immobilization lead to serious secondary complications includ…
NCT04467983 — Abaloparatide Added to Ongoing Denosumab vs Continued Denosumab Alone
| Status | Active, not recruiting |
| Phase | Phase 4 |
| Sponsor | Hospital for Special Surgery, New York |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoporosis, Postmenopausal |
| Interventions | ; |
This randomized open label clinical trial will evaluate the effect of continued denosumab alone over 18 months versus denosumab with added abaloparatide for 18 months. 70 postmenopausal women will be enrolled over a period of 18 months. The co-primary outcomes will be group differences in bone mineral density (BMD) of the total hip and lumbar spine at 18 months. Secondary outcomes will include …
NCT07259811 — Vertebral Augmentation Using VCFix Spinal System in Stand-alone Configuration
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Amber Implants B.V. |
| Enrollment | 10 |
| Study Type | INTERVENTIONAL |
| Conditions | Vertebral Compression Fracture |
| Interventions |
This study will review the safety and possibility of the VCFix Spinal System. This is a proof-of-concept study and an initial review of the surgical procedure and how well the VCFix device works, to who that the VCFix is safe and works well in early testings, so that a larger safety study can be done later to help get CE approval. The VCFix Spinal System will be used in its independent setup, w…
NCT06831994 — Digital Implementation of the German S3 Clinical Practice Guideline for Multimorbidity
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Universitätsklinikum Hamburg-Eppendorf |
| Enrollment | 659 |
| Study Type | INTERVENTIONAL |
| Conditions | Asthma Bronchiale; Breast Neoplasms; Coronary Disease; Diabetes Mellitus, Type 2; Diabetes Mellitus, Type 1 |
| Interventions |
The web application gp-multitool.de is a digital tool for implementing the German S3 clinical practice guideline for multimorbidity of the German Society of General Practitioners and Family Physicians in primary care. The tool enhances evidence-based and patient-centered care by assessing and providing information relevant for the primary care of this patient group. This cluster-randomised clin…
NCT06567054 — Clinical Study to Predict the Risk of Bone Fractures With the POROUS Ultrasound Device
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | POROUS GmbH |
| Enrollment | 1600 |
| Study Type | INTERVENTIONAL |
| Conditions | Healthy; Osteopenia; Osteoporosis |
| Interventions | ; ; |
Osteoporosis is a widespread medical condition among older people. It causes the bones to weaken and become more likely to break. Osteoporosis and bone fracture risk are currently evaluated by looking at clinical risk factors and measuring bone mineral density (BMD). The lower the BMD is, the higher the risk of osteoporotic fractures in the future. However, most bone fractures occur in people w…
NCT06588153 — A Study for the Evaluation of Efficacy and Safety of Prolia® in Participants With Glucocorticoid-induced Osteoporosis in Mainland China
| Status | Active, not recruiting |
| Phase | Phase 4 |
| Sponsor | Amgen |
| Enrollment | 102 |
| Study Type | INTERVENTIONAL |
| Conditions | Glucocorticoid-induced Osteoporosis |
| Interventions |
The main objective of this study is to evaluate the efficacy of Prolia® in improving bone mass density (BMD) of lumbar spine at month 12.
Not Yet Recruiting
NCT07645794 — Clinical Study on a New Diagnostic Strategy for Osteoporosis and Sarcopenia in Chronic Kidney Disease Patients Based on MRI-FF
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Capital Medical University |
| Enrollment | 868 |
| Study Type | OBSERVATIONAL |
| Conditions | Chronic Kidney Disease; Osteoporosis |
| Interventions |
This is a single-center, observational cohort study aiming to validate the diagnostic value of MRI-FF in identifying osteoporosis and sarcopenia in patients with chronic kidney disease (CKD). A total of 868 participants, including 434 CKD patients and 434 non-CKD controls, will be enrolled at Beijing Jishuitan Hospital. All subjects will undergo MRI-FF scans of the lumbar spine and thigh to ass…
NCT07606326 — A Retrospective and Prospective Clinical Registry for Data Collection of Perimenopausal, Menopausal and Premature Ovarian Insufficiency Women
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | IRCCS San Raffaele |
| Enrollment | 5000 |
| Study Type | OBSERVATIONAL |
| Conditions | Menopause; Menopausal Hormone Therapy; Menopause Surgical; Menopause Related Conditions; Menopausal Complaints |
This study is designed as on observational, retrospective, and prospective clinical registry aimed at collecting comprehensive real-world data on women in perimenopause, menopause, and with premature ovarian insufficiency (POI) attending a specialized Menopause Clinic and a Multidisciplinary Outpatient Clinic dedicated to Endocrinology and Metabolic Disorders.
The registry comprises both retro…
NCT07639619 — Robot Assisted Minimally Invasive Treatment Versus Conventional Surgery for FFP3-4 Fragility Fractures of the Pelvis in Elderly Patients
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Junbo Liang |
| Enrollment | 88 |
| Study Type | INTERVENTIONAL |
| Conditions | Fragility Fractures of the Pelvis (FFP); Osteoporosis |
| Interventions | ; |
This prospective randomized controlled trial aims to compare the efficacy and safety of robot assisted minimally invasive treatment versus conventional surgery in elderly patients with FFP3-4 fragility fractures of the pelvis. Eligible patients will be stratified according to FFP classification and randomly assigned in a 1:1 ratio to receive either robot assisted minimally invasive fixation or …
NCT07611097 — Osteoporosis and Sarcopenia Prevention in Middle-Aged Population
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | The University of Hong Kong |
| Enrollment | 8336 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoporosis; Sarcopenia |
| Interventions | ; |
This initiative is designed to yield substantial and multi-level benefits for the Hong Kong community by pioneering a transformative model of preventive healthcare. It represents the largest randomized controlled trial for osteoporosis and sarcopenia prevention in the region, adopting a comprehensive approach to fracture prevention through innovative fitness, lifestyle, and digital strategies. …
NCT07691359 — Osteoporotic Fracture and Lidocaine Plaster 5% for Neuropathic Pain preventioN
| Status | Not yet recruiting |
| Phase | Phase 4 |
| Sponsor | University Hospital, Clermont-Ferrand |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoporotic Vertebral Fracture; Neuropathic Pain |
| Interventions |
Osteoporotic vertebral fractures may lead to chronic pain with a neuropathic component, which is often underdiagnosed and undertreated in older adults. This proof-of-concept randomized controlled trial aims to evaluate whether early application of a 5% lidocaine plaster can prevent the development of neuropathic pain following an osteoporotic vertebral fracture. Participants will be randomized …
NCT07660484 — Link Between ASCorbemia Level and Osteoporosis
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Centre Hospitalier Universitaire de Nice |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoporosis; Vitamin C Deficiency; Vertebral Fractures |
| Interventions |
This monocentric observational study aims to evaluate the association between plasma vitamin C levels (ascorbemia) and the presence of osteoporotic vertebral fractures in patients with osteoporosis. Forty participants will be enrolled at the Rheumatology
Enrolling by Invitation
NCT06811363 — Contribution of Bone to Urine Citrate
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | University of Texas Southwestern Medical Center |
| Enrollment | 25 |
| Study Type | OBSERVATIONAL |
| Conditions | Osteoporosis |
| Interventions | ; ; |
Identification of the mechanisms by which bone contributes to urine citrate could lead to alternative explanations for and approaches to hypocitraturia. This proposal to explore the role of bone in urine citrate addresses the mission of the CMMCR to discover new mechanisms and innovative therapies for diseases of mineral metabolism. The results will be used to apply for extramural funding to fu…
Completed Trials
NCT07660536 — To Study the Efficacy and Safety of Doxercalciferol on Spinal and Femoral Density in Postmenopausal Osteopenic Women in a Long Term 2 Year Study
| Status | Completed |
| Phase | Phase 2 / Phase 3 |
| Sponsor | Creighton University |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoporosis (Senile) |
| Interventions | ; |
A clinical trial to compare the effect of doxercalciferol or placebo in preventing bone loss from the spine and femur in postmenopausal women
NCT00821925 — Estimation of Osteoporosis’ Prevalence in France: Pilot Study in the Department of the Alpes-Maritimes
| Status | Completed |
| Phase | N/A |
| Sponsor | Centre Hospitalier Universitaire de Nice |
| Enrollment | 800 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoporosis |
| Interventions |
The purpose of this study is to estimate Osteoporosis’ prevalence in France and is a pilot study in the Department of the Alpes-Maritimes.
NCT01619722 — Study of a National Cohort of Adult Patients With Phenylketonuria
| Status | Completed |
| Phase | N/A |
| Sponsor | University Hospital, Tours |
| Enrollment | 220 |
| Study Type | OBSERVATIONAL |
| Conditions | PKU; Hyperphenylalaninemia |
Phenylketonuria (PKU) is a metabolic disease of genetic origin. This is a rare disease (incidence 1 / 16000 births) which is the subject of a systematic neonatal screening in France, because it is treatable by a diet low in phenylalanine. This plan is required upon confirmation of diagnosis and continued until the age of 8 years. The current trend is to continue the scheme at least until adoles…
NCT02800278 — Characteristics and Outcomes of Odontoid Fragility Fractures in Elderly
| Status | Completed |
| Phase | N/A |
| Sponsor | Centre Hospitalier Universitaire de Nice |
| Enrollment | 30 |
| Study Type | OBSERVATIONAL |
| Conditions | Odontoid Fracture; Osteoporosis; Surgery |
| Interventions |
Usually, cervical spine fractures are not considered as osteoporotic fractures. However, recent studies show that odontoid fractures are the most common fractures of the cervical spine in elderly and may occur in a context of low trauma energy. Thus, the goal of this observationnal study is :
- to describe the different type of odontoid fracture and to characterize bone status in elderly patie…
NCT02924545 — Evaluation of Osteoporosis Support After a Severe Osteoporotic Fracture in Women Over 50 Years in University Hospital
| Status | Completed |
| Phase | N/A |
| Sponsor | Centre Hospitalier Universitaire de Nīmes |
| Enrollment | 500 |
| Study Type | OBSERVATIONAL |
| Conditions | Osteoporosis |
Evaluate the support of osteoporosis in women over 50 years with severe osteoporotic fractures (hip, vertebral, rib, Humeral, pelvic fractures) in the Nîmes University Hospital taking prediction of treatment of osteoporosis as criterion.
NCT03924414 — Trial of Parkinson’s And Zoledronic Acid
| Status | Completed |
| Phase | Phase 4 |
| Sponsor | California Pacific Medical Center Research Institute |
| Enrollment | 2721 |
| Study Type | INTERVENTIONAL |
| Conditions | Parkinson Disease; Osteoporosis; Parkinsonism; Parkinson’s Disease and Parkinsonism; Atypical Parkinsonism |
| Interventions | ; |
This home-based study is a randomized (1:1) placebo-controlled trial of a single infusion of zoledronic acid-5 mg (ZA) for the prevention of fractures in men and women aged 60 years and older with Parkinson’s disease and parkinsonism with at least 2 years of follow-up. A total of 2650 participants will be enrolled and randomized in the United States. Participants, follow-up outcome assessors, a…
NCT04167163 — Abaloparatide Before Total Knee Arthroplasty
| Status | Completed |
| Phase | Phase 4 |
| Sponsor | University of Wisconsin, Madison |
| Enrollment | 58 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoporosis; Arthroplasties, Knee Replacement |
| Interventions |
The investigator hypothesizes that treating osteoporotic patients with abaloparatide prior to and after total knee arthroplasty will significantly reduce the amount of bone loss.
NCT04384341 — Haemophilia and Bone Loss - PHILEOS Study
| Status | Completed |
| Phase | N/A |
| Sponsor | Centre Hospitalier Universitaire de Saint Etienne |
| Enrollment | 448 |
| Study Type | INTERVENTIONAL |
| Conditions | Hemophilia |
| Interventions | ; |
Haemophilia is a rare bleeding disorder, characterized by factor VIII (HA) or factor IX (HB) deficiency. The absence or the reduction of fVIII or fIX result in impaired thrombin generation and clot formation, causing excessive bleeding (mainly haemarthrosis). Osteoporosis is a systemic bone disease characterized by a low bone mineral density (BMD). A decrease of mean BMD has been described in h…
NCT03926377 — Influence of Dermocorticoids on Bone Mineral Density in Patients With Bullous Pemphigoid
| Status | Completed |
| Phase | Phase 4 |
| Sponsor | Centre Hospitalier Universitaire, Amiens |
| Enrollment | 47 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoporosis; Bullous Pemphigoid |
| Interventions | ; ; |
Bullous pemphigoid is the most common type of bullous skin disease and is clinically characterized by clear-tense bullae, which result in post-bullous cutaneous erosions, altering the skin barrier. The treatment of this pathology consists of the application of high doses of topical corticosteroids (clobetasol propionate) for a prolonged period of at least 6 months. The main objective of this st…
NCT07685392 — Progressive Strength and Balance Exercise for Fall Prevention in Postmenopausal Women With Osteoporosis
| Status | Completed |
| Phase | N/A |
| Sponsor | Instituto Nacional de Rehabilitacion |
| Enrollment | 46 |
| Study Type | INTERVENTIONAL |
| Conditions | Postmenopausal Osteoporosis; Accidental Falls, Aged, Exercise Movement Techniques; Fragility Fractures |
| Interventions | ; |
Postmenopausal osteoporosis increases the risk of fragility fractures, and falls are a major modifiable pathway leading to fracture. This single-blind randomized controlled pilot trial evaluated whether a supervised progressive strength and balance exercise program reduced fall occurrence compared with a conventional home-based exercise program in postmenopausal women with osteoporosis. Women a…
NCT05913219 — Smart Wearable Device (gaitQ): Walk Better Project
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Exeter |
| Enrollment | 98 |
| Study Type | OBSERVATIONAL |
| Conditions | Parkinson Disease; Stroke; Multiple Sclerosis; Osteoporosis; Arthritis |
This study will be underpinned by the new MRC guidelines for developing a complex intervention with a participatory design methodology that uses evidence-based research and behaviour change models alongside COSMIN methodology for validating a measure. Research question: To what extent does gaitQ’s smart cueing system improve people with long-term conditions including people with Parkinson’s (Pw…
NCT07584785 — Mediterranean Diet and Progressive Resistance Training Effects on BMD and Bone Turnover in the Elderly
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Sfax |
| Enrollment | 47 |
| Study Type | INTERVENTIONAL |
| Conditions | Bone Health; Osteoporosis |
| Interventions |
This randomized controlled trial was designed to investigate the effects of progressive resistance training (PRT) combined with a Mediterranean diet on bone mineral density (BMD) and bone turnover markers (BTMs) in older adults.
Participants underwent a detailed medical history assessment, clinical examination, and dietary evaluation. Individuals who met the inclusion criteria provided written…
NCT07245355 — Contribution of Recreational Exercises to Balance and Muscle Strength in Osteoporosis Risk
| Status | Completed |
| Phase | N/A |
| Sponsor | Suleyman Demirel University |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoporosis (Senile) |
| Interventions | ; ; |
This study aims to evaluate the effects of recreational exercises such as Pilates, swimming and walking on muscle strength and balance in women at risk of osteoporosis.
Study hypotheses:
H1: Pilates exercises will be more effective than walking exercises in improving muscle strength among women at risk of osteoporosis.
H2: Swimming exercises will be more effective than walking exercises in i…
Other (Withdrawn)
NCT04253340 — Study of a Bone Assessment Technique, Bone Mineral Analyser, Concerning the Prediction of Improvement in Bone Status After an Infusion of Zoledronic Acid in Osteoporotic Women
| Status | Withdrawn |
| Phase | N/A |
| Sponsor | University Hospital, Rouen |
| Enrollment | N/A |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoporosis |
| Interventions |
- Collection of epidemiological data
- Biological assessment as part of routine care.
- Measurement of the Hurst coefficient at D0
- Measurement of bone density and TBS on D0
- Zoledronic acid infusion the month following inclusion
- phone call at 1 month (observance of zoledronic acid)
- Measurement of bone density, calculation of the Hurst coefficient at M12
NCT05998863 — EffCaMgCit to Prevent Mineral Metabolism and Renal Complications of Chronic PPI Therapy
| Status | Withdrawn |
| Phase | Phase 3 |
| Sponsor | University of Texas Southwestern Medical Center |
| Enrollment | N/A |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoporosis; Hypomagnesemia |
| Interventions | ; |
Proton pump inhibitors (PPIs) are widely used for the control of gastric ulcer-gastritis, erosive esophagitis (gastroesophageal reflux disease), peptic ulcer disease (duodenal ulcer), and heartburn. Despite their efficacy, their use has been implicated in possibly causing fragility fractures (osteoporosis), hypomagnesemia (magnesium deficiency) and increased risk of chronic kidney disease (CKD)…
NCT06973109 — Romosozumab Effects on Bone Density, Muscle Mass, and Spine Surgery Outcomes
| Status | Withdrawn |
| Phase | Phase 2 |
| Sponsor | University of Pittsburgh |
| Enrollment | N/A |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoporosis, Post-menopausal |
| Interventions | ; ; |
The goal of this clinical trial is to learn if romosozumab (Evenity) can improve bone and muscle health in postmenopausal women with osteoporosis who are undergoing lumbar spine surgery. The main questions it aims to answer are:
- Does romosozumab improve bone strength and reduce the risk of complications during and after spine surgery?
- Does romosozumab increase muscle mass and help patients…
NCT05060380 — Feasibility of a Novel Resistance Exercise in Individuals With Osteoporosis
| Status | Withdrawn |
| Phase | N/A |
| Sponsor | University of Alabama at Birmingham |
| Enrollment | N/A |
| Study Type | INTERVENTIONAL |
| Conditions | Osteopenia; Osteoporosis; Postmenopausal Osteoporosis; Sarcopenia |
| Interventions |
The aim of the 2 month randomized controlled trial is to investigate the feasibility of a novel progressive muscle resistance exercise in individuals with low bone mass.