Clinical Trials for Osteoporosis

Currently registered clinical trials for Osteoporosis from ClinicalTrials.gov. 17 recruiting, 50 total studies.

This content is for informational purposes only. Always consult a healthcare professional.

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

StatusRecruiting
PhaseN/A
SponsorNational Institute of Dental and Craniofacial Research (NIDCR)
Enrollment1000
Study TypeOBSERVATIONAL
ConditionsTumor 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

StatusRecruiting
PhaseN/A
SponsorJuin-Hong Cherng
Enrollment146
Study TypeINTERVENTIONAL
ConditionsOsteoporosis; 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

StatusRecruiting
PhaseN/A
SponsorVA Office of Research and Development
Enrollment120
Study TypeINTERVENTIONAL
ConditionsAging; 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

StatusRecruiting
PhasePhase 4
SponsorWake Forest University Health Sciences
Enrollment900
Study TypeINTERVENTIONAL
ConditionsBone 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

StatusRecruiting
PhasePhase 4
SponsorUniversity of Aarhus
Enrollment270
Study TypeINTERVENTIONAL
ConditionsOsteoporosis
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

StatusRecruiting
PhaseN/A
SponsorIstituto Ortopedico Rizzoli
Enrollment120
Study TypeOBSERVATIONAL
ConditionsOsteoporosis; 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

StatusRecruiting
PhasePhase 4
SponsorNational Taiwan University Hospital
Enrollment70
Study TypeINTERVENTIONAL
ConditionsOsteoporosis; 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

StatusRecruiting
PhaseN/A
SponsorIstituto Auxologico Italiano
Enrollment42
Study TypeINTERVENTIONAL
ConditionsOsteoporosis; 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

StatusRecruiting
PhasePhase 4
SponsorPennington Biomedical Research Center
Enrollment50
Study TypeINTERVENTIONAL
ConditionsMusculoskeletal 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

StatusRecruiting
PhaseN/A
SponsorBlueprint Medicines Corporation
Enrollment450
Study TypeOBSERVATIONAL
ConditionsClonal 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

StatusRecruiting
PhaseN/A
SponsorAmber Implants B.V.
Enrollment148
Study TypeINTERVENTIONAL
ConditionsVertebral 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

StatusRecruiting
PhaseN/A
SponsorIstanbul Physical Medicine Rehabilitation Training and Research Hospital
Enrollment65
Study TypeOBSERVATIONAL
ConditionsHemiparesis 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

StatusRecruiting
PhaseN/A
SponsorTaichung Veterans General Hospital
Enrollment1180
Study TypeINTERVENTIONAL
ConditionsOsteoporosis
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

StatusRecruiting
PhaseN/A
SponsorPrecision IO Group
Enrollment60
Study TypeINTERVENTIONAL
ConditionsBone 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

StatusRecruiting
PhaseN/A
SponsorKanuni Sultan Suleyman Training and Research Hospital
Enrollment200
Study TypeOBSERVATIONAL
ConditionsOsteoporosis; 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

StatusRecruiting
PhaseN/A
SponsorMcGill University Health Centre/Research Institute of the McGill University Health Centre
Enrollment28
Study TypeINTERVENTIONAL
ConditionsOsteoporosis
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?

StatusRecruiting
PhaseN/A
SponsorKanuni Sultan Suleyman Training and Research Hospital
Enrollment98
Study TypeOBSERVATIONAL
ConditionsOsteoporosis; 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

StatusActive, not recruiting
PhaseN/A
SponsorNational Taiwan University Hospital
Enrollment600
Study TypeOBSERVATIONAL
ConditionsOsteoporosis; 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

StatusActive, not recruiting
PhaseN/A
SponsorNational Taiwan University Hospital
Enrollment500
Study TypeOBSERVATIONAL
ConditionsOsteoporosis; 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

StatusActive, not recruiting
PhaseN/A
SponsorPenn State University
Enrollment322
Study TypeINTERVENTIONAL
ConditionsPostmenopausal 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

StatusActive, not recruiting
PhaseN/A
SponsorUniversity of Pecs
Enrollment50
Study TypeINTERVENTIONAL
ConditionsSpinal 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

StatusActive, not recruiting
PhasePhase 4
SponsorHospital for Special Surgery, New York
Enrollment70
Study TypeINTERVENTIONAL
ConditionsOsteoporosis, 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

StatusActive, not recruiting
PhaseN/A
SponsorAmber Implants B.V.
Enrollment10
Study TypeINTERVENTIONAL
ConditionsVertebral 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

StatusActive, not recruiting
PhaseN/A
SponsorUniversitätsklinikum Hamburg-Eppendorf
Enrollment659
Study TypeINTERVENTIONAL
ConditionsAsthma 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

StatusActive, not recruiting
PhaseN/A
SponsorPOROUS GmbH
Enrollment1600
Study TypeINTERVENTIONAL
ConditionsHealthy; 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

StatusActive, not recruiting
PhasePhase 4
SponsorAmgen
Enrollment102
Study TypeINTERVENTIONAL
ConditionsGlucocorticoid-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

StatusNot yet recruiting
PhaseN/A
SponsorCapital Medical University
Enrollment868
Study TypeOBSERVATIONAL
ConditionsChronic 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

StatusNot yet recruiting
PhaseN/A
SponsorIRCCS San Raffaele
Enrollment5000
Study TypeOBSERVATIONAL
ConditionsMenopause; 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

StatusNot yet recruiting
PhaseN/A
SponsorJunbo Liang
Enrollment88
Study TypeINTERVENTIONAL
ConditionsFragility 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

StatusNot yet recruiting
PhaseN/A
SponsorThe University of Hong Kong
Enrollment8336
Study TypeINTERVENTIONAL
ConditionsOsteoporosis; 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

StatusNot yet recruiting
PhasePhase 4
SponsorUniversity Hospital, Clermont-Ferrand
Enrollment30
Study TypeINTERVENTIONAL
ConditionsOsteoporotic 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 …

StatusNot yet recruiting
PhaseN/A
SponsorCentre Hospitalier Universitaire de Nice
Enrollment40
Study TypeINTERVENTIONAL
ConditionsOsteoporosis; 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

StatusEnrolling by invitation
PhaseN/A
SponsorUniversity of Texas Southwestern Medical Center
Enrollment25
Study TypeOBSERVATIONAL
ConditionsOsteoporosis
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

StatusCompleted
PhasePhase 2 / Phase 3
SponsorCreighton University
Enrollment60
Study TypeINTERVENTIONAL
ConditionsOsteoporosis (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

StatusCompleted
PhaseN/A
SponsorCentre Hospitalier Universitaire de Nice
Enrollment800
Study TypeINTERVENTIONAL
ConditionsOsteoporosis
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

StatusCompleted
PhaseN/A
SponsorUniversity Hospital, Tours
Enrollment220
Study TypeOBSERVATIONAL
ConditionsPKU; 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

StatusCompleted
PhaseN/A
SponsorCentre Hospitalier Universitaire de Nice
Enrollment30
Study TypeOBSERVATIONAL
ConditionsOdontoid 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

StatusCompleted
PhaseN/A
SponsorCentre Hospitalier Universitaire de Nīmes
Enrollment500
Study TypeOBSERVATIONAL
ConditionsOsteoporosis

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

StatusCompleted
PhasePhase 4
SponsorCalifornia Pacific Medical Center Research Institute
Enrollment2721
Study TypeINTERVENTIONAL
ConditionsParkinson 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

StatusCompleted
PhasePhase 4
SponsorUniversity of Wisconsin, Madison
Enrollment58
Study TypeINTERVENTIONAL
ConditionsOsteoporosis; 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

StatusCompleted
PhaseN/A
SponsorCentre Hospitalier Universitaire de Saint Etienne
Enrollment448
Study TypeINTERVENTIONAL
ConditionsHemophilia
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

StatusCompleted
PhasePhase 4
SponsorCentre Hospitalier Universitaire, Amiens
Enrollment47
Study TypeINTERVENTIONAL
ConditionsOsteoporosis; 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

StatusCompleted
PhaseN/A
SponsorInstituto Nacional de Rehabilitacion
Enrollment46
Study TypeINTERVENTIONAL
ConditionsPostmenopausal 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

StatusCompleted
PhaseN/A
SponsorUniversity of Exeter
Enrollment98
Study TypeOBSERVATIONAL
ConditionsParkinson 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

StatusCompleted
PhaseN/A
SponsorUniversity of Sfax
Enrollment47
Study TypeINTERVENTIONAL
ConditionsBone 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

StatusCompleted
PhaseN/A
SponsorSuleyman Demirel University
Enrollment60
Study TypeINTERVENTIONAL
ConditionsOsteoporosis (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

StatusWithdrawn
PhaseN/A
SponsorUniversity Hospital, Rouen
EnrollmentN/A
Study TypeINTERVENTIONAL
ConditionsOsteoporosis
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

StatusWithdrawn
PhasePhase 3
SponsorUniversity of Texas Southwestern Medical Center
EnrollmentN/A
Study TypeINTERVENTIONAL
ConditionsOsteoporosis; 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

StatusWithdrawn
PhasePhase 2
SponsorUniversity of Pittsburgh
EnrollmentN/A
Study TypeINTERVENTIONAL
ConditionsOsteoporosis, 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

StatusWithdrawn
PhaseN/A
SponsorUniversity of Alabama at Birmingham
EnrollmentN/A
Study TypeINTERVENTIONAL
ConditionsOsteopenia; 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.