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 Fractures from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 21
- Active, not recruiting: 2
- Completed: 12
- Other: 15
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT00870064 — The Treatment of Type I Open Fractures in Pediatrics
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Ann & Robert H Lurie Children’s Hospital of Chicago |
| Enrollment | 300 |
| Study Type | INTERVENTIONAL |
| Conditions | Fractures, Open |
| Interventions | ; |
Open fractures are frequently encountered in orthopaedics. Treatment usually calls for a formal, operative procedure in which the bone is exposed, foreign tissue is debrided and the wound is irrigated. While this is the current standard of care, not all open fractures are equal. In retrospective studies, centers are reporting less aggressive operative management for open fractures may result in…
NCT02390765 — Children s Growth and Behavior Study
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) |
| Enrollment | 1500 |
| Study Type | OBSERVATIONAL |
| Conditions | Obesity; Eating Behaviors; Healthy Volunteers |
Background:
- Studies show that many factors affect children’s eating behavior and health. These include sleep, mood, thinking skills, and genetics. Studying children over time may identify children at higher risk for eating-related health concerns.
Objective:
- To understand how genes and environment influence eating behavior and health over time.
Eligibility:
- Children ages 8-17 in g…
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…
NCT05415384 — Randomized Control Trial, Cryoablation as an Adjunct to Surgical Stabilization of Rib Fractures
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Wake Forest University Health Sciences |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Pain, Postoperative; Rib Fracture Multiple |
| Interventions | ; |
To determine if patients with intraoperative cryoablation have better analgesia results compared to the control group of Surgical Stabilization of Rib Fractures (SSRF) without cryoablation
NCT05131672 — Cast or Operation for Medial Epicondyle Fracture Treatment in Children
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Joseph Janicki |
| Enrollment | 334 |
| Study Type | INTERVENTIONAL |
| Conditions | Fracture Elbow |
| Interventions | ; |
This protocol describes a multicenter, prospective randomized and patient preference cohort superiority trial of medial epicondyle fracture treatments comparing functional outcomes between children treated with operative reduction and fixation or non-operative immobilization.
NCT05131685 — Distal Radius Interventions for Fracture Treatment
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Ann & Robert H Lurie Children’s Hospital of Chicago |
| Enrollment | 334 |
| Study Type | INTERVENTIONAL |
| Conditions | Fracture Distal Radius |
| Interventions | ; |
This protocol describes a multicenter, prospective randomized superiority trial with a patient preference cohort comparing functional outcomes between children treated with sedated reduction versus no formal reduction.
NCT06420141 — The Prevalence of Neuropathic Pain Pathophysiology Associated With Ankle Fracture
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Indiana University |
| Enrollment | 250 |
| Study Type | OBSERVATIONAL |
| Conditions | Neuropathic Pain |
This application addresses the Peer Reviewed Medical Research Program Investigator-Initiated Research Award FY21 W81XWH-22-CPMRP-IIRA area of Chronic Pain Management Research Program- The investigators will utilize subjects who have sustained ankle fractures and may develop chronic pain following bone union. No attempt will be made to affect the experimental outcome in the subjects. This study …
NCT05766670 — Intramedullary Calcium Sulfate Antibiotic Depot
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Wake Forest University Health Sciences |
| Enrollment | 497 |
| Study Type | INTERVENTIONAL |
| Conditions | Open tíbia Fracture; Osteomyelitis Tibia; Tibial Fractures |
| Interventions | ; ; |
The goal of this randomized clinical trial is to study the best treatment for open lower leg fractures to prevent infection. The main questions it aims to answer is if treating tibia fracture patients with a calcium sulfate antibiotic depot is better at preventing infection that the standard of care.
NCT06249126 — Primary Subtalar Arthrodesis for Calcaneal Fractures
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Wake Forest University Health Sciences |
| Enrollment | 218 |
| Study Type | INTERVENTIONAL |
| Conditions | Calcaneus Fracture |
| Interventions | ; |
Management of severe injuries to the heel (displaced intra-articular calcaneus fractures) continues to be a major challenge for orthopedic surgeons. Previous studies have demonstrated poor outcomes, and results show that patients experience long-term pain and decreased quality of life postoperatively. Poor outcomes are driven by pain, in particular, which is linked to post-traumatic subtalar ar…
NCT06679049 — Comparison of Healing Measures Tibial Fractures Following Standard Intramedullary Nailing or Micromotion Tibial Intramedullary Nailing
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Alabama at Birmingham |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Tibial Fractures |
| Interventions | ; |
The primary purpose of this study is to perform a high-quality randomized control trial comparing intramedullary tibial nail fixation with standard design nails to a micromotion tibial nail device, to evaluate the rates of union and post-operative outcomes.
NCT07678034 — Post-Market Clinical Follow-Up (PMCF) Study Evaluating the Safety and Efficacy of Tıpmed™ Shoulder Prosthesis System
| Status | Recruiting |
| Phase | N/A |
| Sponsor | TIPMED Medical Device Manufacturing Ltd. Co. |
| Enrollment | 54 |
| Study Type | OBSERVATIONAL |
| Conditions | Glenohumeral Osteoarthritis; Proximal Humerus Fracture; Rotator Cuff Arthropathy; Rheumatoid Arthritis; Avascular Necrosis |
| Interventions | ; |
This study is designed as a prospective, multicenter, observational post-market clinical follow-up (PMCF) study to evaluate the safety and effectiveness of the Tipmed™ Shoulder Prosthesis System at 12 months postoperatively. The study population includes adult patients who undergo reverse shoulder arthroplasty (RSA) or shoulder hemiarthroplasty (HA) using the Tipmed™ implant systems due to vari…
NCT07683715 — Virtual Reality-Assisted Cast Application in Children With Forearm Fractures
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Başakşehir Çam & Sakura City Hospital |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Forearm Fractures; Procedural Anxiety; Doctor-Related Fear |
| Interventions | ; |
This prospective randomized controlled trial will evaluate whether virtual reality can reduce procedural distress in children undergoing cast application for forearm fractures. Children will be assigned to either a virtual reality group or a standard care group. In the virtual reality group, children will watch a 3-minute child-friendly animated educational video using a VR headset during cast …
NCT07244211 — MAPT Protocol: Fixation Versus Arthroplasty Surgical Treatments for Early Recovery After HIP Fracture (FASTER-HIP)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Southern California |
| Enrollment | 600 |
| Study Type | INTERVENTIONAL |
| Conditions | Femoral Neck Fractures |
| Interventions | ; |
This study is an intervention domain of the Musculoskeletal Adaptive Platform Trial. The primary goal of this pragmatic, randomized, open-label, comparative effectiveness trial is to evaluate if arthroplasty is superior to internal fixation when used to treat minimally displaced femoral neck fractures in older adults ≥60 years old. We hypothesize that arthroplasty will reduce death, preserve am…
NCT06885359 — CoCrMo LOCK Bipolar Femoral Heads FU
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Limacorporate S.p.a |
| Enrollment | 60 |
| Study Type | OBSERVATIONAL |
| Conditions | Femoral Fractures; Hip Arthropathy |
Study design: monocentric, retrospective, observational and post-market clinical study.
Purpose: To demonstrate the safety and performance of CoCrMo LOCK bipolar femoral heads. The eligible study population is represented by the entire population that underwent a hip replacement with CoCrMo LOCK bipolar femoral heads from 1st January 2023 onwards at the site in accordance with the indication f…
NCT07430345 — Buprenorphine for Analgesia in Older Adults With Acute Fractures in the Emergency Department
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | The Cooper Health System |
| Enrollment | 48 |
| Study Type | INTERVENTIONAL |
| Conditions | Fracture |
| Interventions | ; |
The goal of this clinical trial is to learn if buprenorphine can treat pain in older adults who have broken bones. The main questions it aims to answer are:
Is buprenorphine as effective as opioids to treat pain? Are there less side effects with buprenorphine? Researchers will compare buprenorphine and hydromorphone to see if there are differences in pain control and side effects.
Participant…
NCT07538323 — Wrist Injury Strengthening Exercise (WISE) Versus Usual Care Advice for Improving Pain and Function
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Aarhus |
| Enrollment | 588 |
| Study Type | INTERVENTIONAL |
| Conditions | Distal Radius Fracture; Colles Fracture; Wrist Fracture; Wrist Fractures; Fracture Arm |
| Interventions | ; |
The goal of this clinical trial is to find out whether a therapist-guided exercise program helps people aged 50 and older recover better, in terms of pain and function, after a wrist fracture, compared to the usual care advice they would normally receive. The main question it aims to answer is:
• Will participants who receive a therapist-supervised exercise program have better improvement in p…
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…
NCT07548567 — A Long Axis Approach to the Femoral Artery Block (FAB) for Managing Tourniquet Pain and Hypertension in Below-the-Knee Fracture Surgery
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National and Kapodistrian University of Athens |
| Enrollment | 84 |
| Study Type | INTERVENTIONAL |
| Conditions | Tourniquet Hypertension |
| Interventions | ; ; |
This is a prospective, randomized, double-blind controlled trial evaluating an ultrasound-guided femoral artery block (FAB) using a long-axis in-plane approach compared with a short-axis approach and a control group.
The study will include adult patients (ASA I-III) undergoing below-the-knee fracture surgery with tourniquet application. All patients will receive standardized anesthesia includi…
NCT07687290 — Comparative Study Between Pericapsular Nerve Group Block (PENG) And Pericapsular Nerve Group (PENG) Block Combined With Lateral Femoral Cutaneous Nerve (LFCN) Block for Positioning Analgesia Prior to Spinal Anesthesia in Hip Fracture Patients
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Ain Shams University |
| Enrollment | 24 |
| Study Type | INTERVENTIONAL |
| Conditions | Hip Fracture Surgeries |
| Interventions | ; ; |
To evaluate and compare the effectiveness of the Pericapsular Nerve Group (PENG) block alone versus the PENG block combined with the Lateral Femoral Cutaneous Nerve (LFCN) block in providing adequate analgesia for patient positioning during spinal anesthesia in individuals undergoing surgery for hip fracture.
NCT07552766 — A Clinical Trial on the Use of Lidocaine Infusion During Surgery for Pediatric Upper Extremity Fractures and Its Impact on Total Perioperative Opioid Requirements
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Nemours Children’s Clinic |
| Enrollment | 90 |
| Study Type | INTERVENTIONAL |
| Conditions | Fracture Arm; Fracture Closed of Lower End of Forearm, Unspecified; Fracture Elbow; Fracture Fixation; Fracture Fixation, Internal |
| Interventions | ; |
This study is a prospective, randomized, double-blind clinical trial evaluating whether intraoperative intravenous lidocaine infusion (IVLI) reduces opioid requirements and improves postoperative pain control in children undergoing surgical fixation of upper extremity long bone fractures under general anesthesia. Ninety pediatric patients, ages 3-18 will be enrolled and randomized 1:1 to receiv…
NCT07453537 — Cranberry Polyphenols and Stress Resilience During Multitasking in Healthy Adults
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Florida |
| Enrollment | 84 |
| Study Type | INTERVENTIONAL |
| Conditions | Stress Response; Mental Stress; Multitasking Behavior and Multitasking Ability; Physiological Stress; Cognitive Symptoms |
| Interventions | ; |
This randomized, double-blind, placebo-controlled clinical trial evaluates whether 70 days of daily cranberry juice consumption improves cognitive performance and motor accuracy and reduces psychological and physiological stress responses during a motor-cognitive dual-task multitasking challenge in healthy adults aged 30-55 (Aim 1). It is hypothesized that chronic cranberry juice intake will en…
Active, Not Recruiting
NCT05583864 — Lumbar Fusion With Porous Versus Non-Porous Cages
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Francis Farhadi |
| Enrollment | 108 |
| Study Type | INTERVENTIONAL |
| Conditions | Spinal Fusion; Lumbar Fusion; Arthrodesis; Spondylolisthesis; Pseudarthrosis |
| Interventions | ; |
The objective of this single site, randomized controlled trial is to assess and compare radiographic and clinical outcomes in patients who are to undergo lumbar interbody fusion procedures (TLIF), supplemented with pedicle screw instrumentation, using one of the following interventions:
- Porous titanium cages
- Non-porous titanium-coated poly-ether-ether-ketone (PEEK) cages.
NCT05742932 — Prospective Study to Evaluate the Performance and the Safety of Global D’s Implants of Craniomaxillofacial Surgery (CMF) Ranges Indicated for Trauma Surgery (CMF-TRAUMA)
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Global D |
| Enrollment | 99 |
| Study Type | OBSERVATIONAL |
| Conditions | Trauma Injury; Maxilla Fracture; Maxillofacial Trauma |
| Interventions |
This study is set up within the framework of the European Union regulation 2017/745 on medical devices. Its objective is to confirm the performance and safety of the Global D implants (ORTRAUTEK® and MINITEK/MICROTEK®) used for trauma surgery.
Not Yet Recruiting
NCT07674043 — MY01 Pressure Monitoring in Adolescent Tibia Fractures
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Boston Children’s Hospital |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Proximal Tibia Fracture; Tibial Shaft Fracture; Acute Compartment Syndrome |
| Interventions |
The goal of this clinical trial is to learn more about anterior leg compartment pressures in adolescents who have sustained tibia fractures. It will also examine whether measuring anterior compartment pressure helps physicians diagnose acute compartment syndrome (ACS), a rare but dangerous complication that can develop following surgical treatment of a tibia fracture.
The main questions it aim…
NCT07671183 — Effect of Adipose Tissue Derived Autologous Mesenchymal Stem Cell Concentrate on Bone Quality in Mandibular Fracture Healing.
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Cairo University |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Mandible Fracture |
| Interventions | ; |
- The goal of study is to evaluate the effectiveness of adipose tissue derived-MSCs concentrate application in mandibular fractures. The main question it aims to answer is: Does intervention enhance bone quality, reduce complications and reduce bone regeneration time.
- Researchers will compare the effectiveness of adipose tissue derived-MSCs concentrate application with ORIF to ORIF alone to s…
NCT07237191 — Geriatric Distal Femur
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Wake Forest University Health Sciences |
| Enrollment | 256 |
| Study Type | INTERVENTIONAL |
| Conditions | Articular Fractures |
| Interventions | ; |
The goal of this clinical trial is to compare two types of surgical fixation in patients with specific kinds of distal femur fractures. The main questions it aims to answer is which operation for distal femur fractures is better for efficient return to work and everyday activities.
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 …
NCT07676734 — Comparison of Three Analgesic Strategies for Hip Fracture Surgery
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Başakşehir Çam & Sakura City Hospital |
| Enrollment | 90 |
| Study Type | INTERVENTIONAL |
| Conditions | Hip Fracture |
| Interventions | ; ; |
Hip fracture surgery is associated with significant postoperative pain and increased opioid requirements. Regional anesthesia techniques may improve analgesia and reduce opioid consumption. This prospective, randomized, double-blind, controlled trial aims to compare the postoperative analgesic efficacy of Quadro-Iliac Plane Block (QIPB), Suprainguinal Fascia Iliaca Block (SIFIB), and standard a…
NCT07668531 — Kinesiophobia and Functional Outcomes in Distal Radius Fractures
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Ebru Aloğlu Çiftçi |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Distal Radius Fracture |
| Interventions |
Distal radius fractures are among the most common fractures in adults and are frequently treated with closed reduction and cast immobilization. Although fracture healing is generally successful, some patients may develop fear of movement (kinesiophobia) after cast removal because of pain, reinjury concerns, or reduced confidence in using the injured wrist.
The purpose of this study is to evalu…
NCT07475975 — The Effect of the Cold Arm Sling Elevation Pillow on Postoperative Anxiety and Comfort in Children
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Istanbul University - Cerrahpasa |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Upper Extremity Fractures; Postoperative Anxiety; Patient Comfort |
| Interventions | ; |
The purpose of this clinical trial is to learn whether the use of a “cold and arm sling elevation pillow” affects anxiety and comfort levels in children aged 7-12 years undergoing surgery for upper extremity fractures. The main questions it aims to answer are:
- Does the use of a cold and arm sling elevation pillow reduce postoperative anxiety levels in children?
- Does the use of a cold and a…
NCT07687108 — Improving Shared DECISion-making in oldEr Hip Fracture Patients Living With Frailty
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | University of Southampton |
| Enrollment | 42 |
| Study Type | OBSERVATIONAL |
| Conditions | Hip Fractures (i.e. Femoral Neck or Intertrochanteric Hip Fractures); Hip Fractures (ICD-10 72.01-72.2); Hip Fracture; Hip Fracture, Post Surgery Recovery, Muscle Resilience |
Title Improving shared decision-making in older hip fracture patients living with frailty
Aim To use routinely information normally collected by the NHS, and interviews with patients, families, and healthcare professionals, to produce an aid to help patients make decisions about hip fracture treatment that reflects what is important to them.
Background Breaking a hip after a fall is common in…
NCT07659184 — IRONCARE: Iron Treatment in Older Patients With Hip Fractures
| Status | Not yet recruiting |
| Phase | Phase 4 |
| Sponsor | University of Aarhus |
| Enrollment | 528 |
| Study Type | INTERVENTIONAL |
| Conditions | Hip Fracture; Anemia; Iron; Placebo - Control |
| Interventions | ; ; |
The aim of this study is to investigate the effects of intravenous (IV) iron therapy compared to alternate-day oral iron treatment and no supplementation in older patients with hip fractures. This study will examine the impact of iron treatment on fatigue, functional decline, fear of falling, cognitive impairment, and quality of life, as well as its effects on iron stores and hemoglobin levels,…
NCT07672184 — Degenerative Changes After Treatment of Thoracolumbar Junction Fractures
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Sklifosovsky Institute of Emergency Care |
| Enrollment | 150 |
| Study Type | OBSERVATIONAL |
| Conditions | Thoracolumbar Spine Fracture; Facet Joint Degeneration; Intervertebral Disc Degeneration |
This observational study will evaluate how degenerative changes in the facet joints and intervertebral discs develop over time after treatment of AOSpine type A2, A3, and A4 fractures of the thoracolumbar junction. Patients treated conservatively and patients treated surgically will be compared with each other and with a control group of patients who underwent repeated computed tomography exami…
Enrolling by Invitation
NCT05501834 — Anxiety Surrounding Supracondylar Pin Removal in Children: A Randomized Controlled Trial
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | Boston Children’s Hospital |
| Enrollment | 140 |
| Study Type | INTERVENTIONAL |
| Conditions | Supracondylar Humerus Fracture; Anxiety |
| Interventions | ; ; |
This study aims to determine if removing supracondylar pins immediately following cast removal and prior to X-ray and/or using a VR headset during pin removal decreases patient and parent/guardian anxiety compared to pin removal following cast removal and X-ray and/or without the use of a VR headset. The research team hypothesizes that patient anxiety response will be lower when pins are remove…
NCT07679009 — Diagnostic Utility of Cardiac MRI
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | Baylor Research Institute |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Abandoned Endocardial Leads; Broken Endocardial Leads; Permanent Epicardial Leads |
| Interventions |
This is a prospective cohort study looking to systematically evaluate the safety of conducting cardiac Magnetic Resonance Imaging (MRI) in this high-risk patient group with abandoned, fractured endocardial leads or surgically implanted permanent epicardial leads, by monitoring clinical outcome and device functionality (if active device present).
Completed Trials
NCT00076830 — Evaluation and Treatment of Patients With Connective Tissue Disease
| Status | Completed |
| Phase | N/A |
| Sponsor | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) |
| Enrollment | 180 |
| Study Type | OBSERVATIONAL |
| Conditions | Connective Tissue Disorders; Osteogenesis Imperfecta; Bone Diseases, Metabolic; Melorheostosis |
This study offers evaluation and treatment of patients with a suspected connective tissue disorder. The protocol is not designed to test new treatments; rather, patients receive standard care. The study is designed to: 1) allow NICHD’s staff to learn more about connective tissue disorders, 2) train physicians in the evaluation and treatment of these disorders; and 3) establish a pool of patient…
NCT02227446 — Local Antibiotic Therapy to Reduce Infection After Operative Treatment of Fractures at High Risk of Infection: A Multicenter Randomized, Controlled Trial (VANCO)
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | Major Extremity Trauma Research Consortium |
| Enrollment | 1036 |
| Study Type | INTERVENTIONAL |
| Conditions | Post Operative Surgical Site Infection |
| Interventions |
The Vancomycin Study is a multi-center, prospective randomized controlled trial that will compare the proportion of deep surgical site infections within 6 months in patients treated with local Vancomycin powder compared to those treated without local Vancomycin powder at the time of fracture fixation.
NCT04015128 — A Post-Market Clinical Evaluation of the Treatment of Femur Fractures With the Femoral Nail GT
| Status | Completed |
| Phase | N/A |
| Sponsor | Stryker Trauma and Extremities |
| Enrollment | 66 |
| Study Type | OBSERVATIONAL |
| Conditions | Femoral Fracture |
| Interventions |
This investigation is a prospective, multi-center clinical investigation. It is anticipated that a total of 50 subjects will be enrolled. Neither subjects nor investigators are blinded to treatment and the clinical investigation includes a historical control which will be compared to the Femoral Nail GT of the T2 Alpha Femur Antegrade GT/PF Nailing System.
Total duration of enrollment, 12 mont…
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…
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…
NCT07256405 — Metagenomic Next-Generation Sequencing for the Diagnosis of Fracture-related Infection
| Status | Completed |
| Phase | N/A |
| Sponsor | Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer |
| Enrollment | 100 |
| Study Type | OBSERVATIONAL |
| Conditions | Infection; Fracture; Bone |
| Interventions |
The value of next-generation sequencing (NGS) using Nanopore technology has been demonstrated in the case of diabetic patients’ wounds or in prosthetic joint infections. The aim of this study is to demonstrate its relevance as a new diagnostic approach for fracture-related infections (FRI).
Bone samples from patient with FRI will be submitted to shotgun metagenomic Next-generation sequencing u…
NCT06661785 — Interlocking Polyetheretherketone Implants for Orbital Floor Reconstruction
| Status | Completed |
| Phase | N/A |
| Sponsor | Tanta University |
| Enrollment | 22 |
| Study Type | INTERVENTIONAL |
| Conditions | Large Orbital Floor Fracture |
| Interventions |
Patients with large orbital floor fracture were reconstructed with interlocking polyetheretherketone patient-specific implant and will be evaluated clinically and radiographically
NCT06096883 — Hip Socket Erosion Study
| Status | Completed |
| Phase | N/A |
| Sponsor | Rijnstate Hospital |
| Enrollment | 134 |
| Study Type | OBSERVATIONAL |
| Conditions | Femoral Neck Fractures; Hemiarthroplasty; Acetabulum; Protrusion |
The aim of this exploratory retrospective study is to gain a better understanding about the occurrence of acetabular erosion in patients after after hip hemiarthroplasty. The main objectives are i) to summarise a selection of basic patient characteristics of all patients of ≤ 75 years of age with a femoral neck fracture who have received either HA or THA, ii) to explore the proportion of patien…
NCT07351084 — Patient Factors Associated With Fragmentation of Copper Intrauterine Device (IUD) Requiring Hysteroscopic Removal
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Kansas Medical Center |
| Enrollment | 44 |
| Study Type | OBSERVATIONAL |
| Conditions | Intrauterine Device Complications; Contraceptive Device Failure; IUD Fragmentation; Retained Intrauterine Device; Female Contraception |
The purpose of this retrospective chart review was to identify risks factors for patients associated to Cooper IUD fragmentation upon removal resulting in the requirement of a hysteroscopy evaluation.
NCT07081113 — Study Comparing Cyriax Mobilization and Muscle Energy Techniques for Improving Arm Function in People Recovering From Surgery for Distal Radius (Wrist) Fractures
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Lahore |
| Enrollment | 76 |
| Study Type | INTERVENTIONAL |
| Conditions | Distal Radius Fracture Fixation; Stiffness of Hand, Not Elsewhere Classified |
| Interventions | ; |
This study aims to compare the effects of Cyriax Mobilization and Muscle Energy Techniques (METs) on functional recovery in patients who have undergone surgical fixation of distal radius fractures. A total of 76 participants between 18 and 40 years old will be randomly assigned to two groups. One group will receive Cyriax Mobilization with conventional therapy, while the other will receive METs…
NCT07673991 — Diagnostic Reliability of ChatGPT in Letournel-Judet Acetabular Fracture Classification
| Status | Completed |
| Phase | N/A |
| Sponsor | Ankara City Hospital Bilkent |
| Enrollment | 184 |
| Study Type | OBSERVATIONAL |
| Conditions | Acetabular Fractures; Pelvic Injury |
| Interventions |
This study aims to evaluate the diagnostic reliability of the multimodal artificial intelligence model ChatGPT-4o in classifying acetabular fractures using the Letournel-Judet classification system. The study retrospectively analyzed standardized pelvic radiographs (anteroposterior, iliac oblique, and obturator oblique) from 184 patients presenting with pelvic injuries. The diagnostic performan…
NCT07669714 — Comparison of Debridement, Antibiotic, Implant Retention and Implant Exchange in Early-stage Fracture-related Infections
| Status | Completed |
| Phase | N/A |
| Sponsor | Antalya Health Sciences University |
| Enrollment | 94 |
| Study Type | OBSERVATIONAL |
| Conditions | Orthopedic Surgery; Fracture Related Infection; Debridement; Implant Retention; Implant Removal/Replacement |
| Interventions | ; |
This study aims to compare the clinical outcomes of debridement, antibiotics, and implant retention (DAIR) and implant removal/replacement methods used in the treatment of fracture-related infections, and to determine the infection-free fracture healing rates and the factors affecting treatment success.
Other (Terminated)
NCT05714631 — Lidocaine Patches in Elderly Patients With Traumatic Rib Fractures
| Status | Terminated |
| Phase | Phase 4 |
| Sponsor | Medical College of Wisconsin |
| Enrollment | 5 |
| Study Type | INTERVENTIONAL |
| Conditions | Rib Fractures |
| Interventions | ; |
Many patients are prescribed lidocaine patches for rib fractures despite mixed evidence to their efficacy. The outcome of this trial offers significant benefit to patient care if it finds benefit of their use or if it does not. Reducing opioid use and increasing functional outcomes in geriatric patient suffering rib fractures can improve quality of life and ability to return to prior levels of …
Other (Suspended)
NCT06066619 — Can Cranberry Juice Enhance the Cognition Accuracy and Alleviate Negative Mental Consequences During Multitasking?
| Status | Suspended |
| Phase | N/A |
| Sponsor | University of Florida |
| Enrollment | 126 |
| Study Type | INTERVENTIONAL |
| Conditions | Stress Response; Multitasking Behavior; Mental Stress; Physiological Stress; Cognitive Symptom |
| Interventions | ; ; |
This clinical trial aims to investigate the effects of a 70-day consumption of cranberry juice on cognitive and motor accuracy, mental and physiological stress, and stress response in healthy men and women between the ages of 30 and 55 who engage in multitasking. The trial will utilize a randomized, double-blinded, placebo-controlled design. It is worth noting that studies have shown that over …
Other (Withdrawn)
NCT04314570 — Saphenous Nerve Block After Tibial Plateau ORIF
| Status | Withdrawn |
| Phase | N/A |
| Sponsor | Stanford University |
| Enrollment | N/A |
| Study Type | INTERVENTIONAL |
| Conditions | Tibial Plateau Fracture; Pain, Postoperative |
| Interventions | ; |
Fractures of the tibial plateau, while very painful, typically do not receive nerve blocks. This is because of a concern that the numbness from a nerve block would “mask” the typically painful symptoms of compartment syndrome, a condition that can lead to a permanent loss of function of the injured limb. Our study aims to evaluate the effectiveness of saphenous nerve block for pain management a…