Clinical Trials for Fractures

Currently registered clinical trials for Fractures from ClinicalTrials.gov. 21 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 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

StatusRecruiting
PhaseN/A
SponsorAnn & Robert H Lurie Children’s Hospital of Chicago
Enrollment300
Study TypeINTERVENTIONAL
ConditionsFractures, 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

StatusRecruiting
PhaseN/A
SponsorEunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Enrollment1500
Study TypeOBSERVATIONAL
ConditionsObesity; 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

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…

NCT05415384 — Randomized Control Trial, Cryoablation as an Adjunct to Surgical Stabilization of Rib Fractures

StatusRecruiting
PhaseN/A
SponsorWake Forest University Health Sciences
Enrollment80
Study TypeINTERVENTIONAL
ConditionsPain, 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

StatusRecruiting
PhaseN/A
SponsorJoseph Janicki
Enrollment334
Study TypeINTERVENTIONAL
ConditionsFracture 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

StatusRecruiting
PhaseN/A
SponsorAnn & Robert H Lurie Children’s Hospital of Chicago
Enrollment334
Study TypeINTERVENTIONAL
ConditionsFracture 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

StatusRecruiting
PhaseN/A
SponsorIndiana University
Enrollment250
Study TypeOBSERVATIONAL
ConditionsNeuropathic 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

StatusRecruiting
PhasePhase 3
SponsorWake Forest University Health Sciences
Enrollment497
Study TypeINTERVENTIONAL
ConditionsOpen 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

StatusRecruiting
PhaseN/A
SponsorWake Forest University Health Sciences
Enrollment218
Study TypeINTERVENTIONAL
ConditionsCalcaneus 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

StatusRecruiting
PhaseN/A
SponsorUniversity of Alabama at Birmingham
Enrollment100
Study TypeINTERVENTIONAL
ConditionsTibial 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

StatusRecruiting
PhaseN/A
SponsorTIPMED Medical Device Manufacturing Ltd. Co.
Enrollment54
Study TypeOBSERVATIONAL
ConditionsGlenohumeral 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

StatusRecruiting
PhaseN/A
SponsorBaşakşehir Çam & Sakura City Hospital
Enrollment120
Study TypeINTERVENTIONAL
ConditionsForearm 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)

StatusRecruiting
PhaseN/A
SponsorUniversity of Southern California
Enrollment600
Study TypeINTERVENTIONAL
ConditionsFemoral 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

StatusRecruiting
PhaseN/A
SponsorLimacorporate S.p.a
Enrollment60
Study TypeOBSERVATIONAL
ConditionsFemoral 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

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorThe Cooper Health System
Enrollment48
Study TypeINTERVENTIONAL
ConditionsFracture
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

StatusRecruiting
PhaseN/A
SponsorUniversity of Aarhus
Enrollment588
Study TypeINTERVENTIONAL
ConditionsDistal 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?

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…

NCT07548567 — A Long Axis Approach to the Femoral Artery Block (FAB) for Managing Tourniquet Pain and Hypertension in Below-the-Knee Fracture Surgery

StatusRecruiting
PhaseN/A
SponsorNational and Kapodistrian University of Athens
Enrollment84
Study TypeINTERVENTIONAL
ConditionsTourniquet 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

StatusRecruiting
PhaseN/A
SponsorAin Shams University
Enrollment24
Study TypeINTERVENTIONAL
ConditionsHip 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

StatusRecruiting
PhasePhase 4
SponsorNemours Children’s Clinic
Enrollment90
Study TypeINTERVENTIONAL
ConditionsFracture 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

StatusRecruiting
PhaseN/A
SponsorUniversity of Florida
Enrollment84
Study TypeINTERVENTIONAL
ConditionsStress 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

StatusActive, not recruiting
PhaseN/A
SponsorFrancis Farhadi
Enrollment108
Study TypeINTERVENTIONAL
ConditionsSpinal 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:

  1. Porous titanium cages
  2. 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)

StatusActive, not recruiting
PhaseN/A
SponsorGlobal D
Enrollment99
Study TypeOBSERVATIONAL
ConditionsTrauma 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

StatusNot yet recruiting
PhaseN/A
SponsorBoston Children’s Hospital
Enrollment50
Study TypeINTERVENTIONAL
ConditionsProximal 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.

StatusNot yet recruiting
PhaseN/A
SponsorCairo University
Enrollment20
Study TypeINTERVENTIONAL
ConditionsMandible 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

StatusNot yet recruiting
PhaseN/A
SponsorWake Forest University Health Sciences
Enrollment256
Study TypeINTERVENTIONAL
ConditionsArticular 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

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 …

NCT07676734 — Comparison of Three Analgesic Strategies for Hip Fracture Surgery

StatusNot yet recruiting
PhaseN/A
SponsorBaşakşehir Çam & Sakura City Hospital
Enrollment90
Study TypeINTERVENTIONAL
ConditionsHip 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

StatusNot yet recruiting
PhaseN/A
SponsorEbru Aloğlu Çiftçi
Enrollment100
Study TypeINTERVENTIONAL
ConditionsDistal 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

StatusNot yet recruiting
PhaseN/A
SponsorIstanbul University - Cerrahpasa
Enrollment80
Study TypeINTERVENTIONAL
ConditionsUpper 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

StatusNot yet recruiting
PhaseN/A
SponsorUniversity of Southampton
Enrollment42
Study TypeOBSERVATIONAL
ConditionsHip 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

StatusNot yet recruiting
PhasePhase 4
SponsorUniversity of Aarhus
Enrollment528
Study TypeINTERVENTIONAL
ConditionsHip 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

StatusNot yet recruiting
PhaseN/A
SponsorSklifosovsky Institute of Emergency Care
Enrollment150
Study TypeOBSERVATIONAL
ConditionsThoracolumbar 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

StatusEnrolling by invitation
PhaseN/A
SponsorBoston Children’s Hospital
Enrollment140
Study TypeINTERVENTIONAL
ConditionsSupracondylar 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

StatusEnrolling by invitation
PhaseN/A
SponsorBaylor Research Institute
Enrollment20
Study TypeINTERVENTIONAL
ConditionsAbandoned 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

StatusCompleted
PhaseN/A
SponsorEunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Enrollment180
Study TypeOBSERVATIONAL
ConditionsConnective 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)

StatusCompleted
PhasePhase 3
SponsorMajor Extremity Trauma Research Consortium
Enrollment1036
Study TypeINTERVENTIONAL
ConditionsPost 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

StatusCompleted
PhaseN/A
SponsorStryker Trauma and Extremities
Enrollment66
Study TypeOBSERVATIONAL
ConditionsFemoral 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

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…

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…

StatusCompleted
PhaseN/A
SponsorCentre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Enrollment100
Study TypeOBSERVATIONAL
ConditionsInfection; 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

StatusCompleted
PhaseN/A
SponsorTanta University
Enrollment22
Study TypeINTERVENTIONAL
ConditionsLarge 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

StatusCompleted
PhaseN/A
SponsorRijnstate Hospital
Enrollment134
Study TypeOBSERVATIONAL
ConditionsFemoral 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

StatusCompleted
PhaseN/A
SponsorUniversity of Kansas Medical Center
Enrollment44
Study TypeOBSERVATIONAL
ConditionsIntrauterine 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

StatusCompleted
PhaseN/A
SponsorUniversity of Lahore
Enrollment76
Study TypeINTERVENTIONAL
ConditionsDistal 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

StatusCompleted
PhaseN/A
SponsorAnkara City Hospital Bilkent
Enrollment184
Study TypeOBSERVATIONAL
ConditionsAcetabular 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…

StatusCompleted
PhaseN/A
SponsorAntalya Health Sciences University
Enrollment94
Study TypeOBSERVATIONAL
ConditionsOrthopedic 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

StatusTerminated
PhasePhase 4
SponsorMedical College of Wisconsin
Enrollment5
Study TypeINTERVENTIONAL
ConditionsRib 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?

StatusSuspended
PhaseN/A
SponsorUniversity of Florida
Enrollment126
Study TypeINTERVENTIONAL
ConditionsStress 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

StatusWithdrawn
PhaseN/A
SponsorStanford University
EnrollmentN/A
Study TypeINTERVENTIONAL
ConditionsTibial 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…