Clinical Trials for Joint Disorders

Currently registered clinical trials for Joint Disorders from ClinicalTrials.gov. 16 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 Joint Disorders from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 16
  • Active, not recruiting: 9
  • Completed: 17
  • Other: 8

Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.

Recruiting Trials

NCT00024479 — Studies of the Natural History of Rheumatic Diseases

StatusRecruiting
PhaseN/A
SponsorNational Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Enrollment7500
Study TypeOBSERVATIONAL
ConditionsRheumatic Diseases; Arthritis

This study will explore the causes of rheumatic diseases and why many of them affect certain minority communities more severely. Rheumatic diseases may cause joint pain, stiffness or swelling. Some can involve bones, muscles, tendons or ligaments. Some cause abnormalities of the immune system-the body s defense against disease. Some rheumatic diseases are painful or deforming and some can be li…

NCT00051857 — MRI Study of Musculoskeletal Function

StatusRecruiting
PhaseN/A
SponsorNational Institutes of Health Clinical Center (CC)
Enrollment750
Study TypeOBSERVATIONAL
ConditionsAbnormalities; Imaging; Patellofemoral Pain Syndrome

This study will use magnetic resonance imaging (MRI) and ultrasound images to study how muscles, tendons, and bones work together to cause motion. The procedure is one of several tools being developed to characterize normal and impaired musculoskeletal function, with the goal of developing improved methods of diagnosis and treatment of movement disorders.

Healthy normal volunteers must be age …

NCT01422694 — Natural History and Development of Spondyloarthritis

StatusRecruiting
PhaseN/A
SponsorNational Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Enrollment2000
Study TypeOBSERVATIONAL
ConditionsArthritis; Spondylitis, Ankylosing

Background:

- Spondyloarthritis (SpA) is a group of bone and joint disorders that may cause back and joint pain and stiffness. In some cases, SpA can lead to abnormal bone growth affecting the joints and spine. Some patients have SpA without ever developing these growths, while others develop them after only a few years. Researchers are interested in studying people with SpA and their relativ…

NCT06214923 — Neural Mechanisms of Immersive Virtual Reality in Chronic Pain (VR TMD EEG)

StatusRecruiting
PhaseN/A
SponsorUniversity of Maryland, Baltimore
Enrollment78
Study TypeINTERVENTIONAL
ConditionsPain; Virtual Reality; Placebo; Temporomandibular Disorder
Interventions; ;

This project examines, in chronic pain, the mechanisms of immersive virtual reality compared to the mechanisms of placebo hypoalgesia. The potential of developing new non-pharmacological premises for low-risk interventions for pain management is high.

NCT06491745 — Is Adding Extracorporeal Shock Wave Therapy to Physiotherapy and Corticosteroid Injection Beneficial for Frozen Shoulder

StatusRecruiting
PhaseN/A
SponsorShin Kong Wu Ho-Su Memorial Hospital
Enrollment94
Study TypeINTERVENTIONAL
ConditionsFrozen Shoulder; Corticosteroid Injection; Physical Therapy; Extracorporeal Shock Wave Therapy; Rehabilitation
Interventions;

Frozen shoulder, or adhesive capsulitis of the shoulder, is a common clinical problem characterized by pain, loss of both passive and active range of motion (ROM) of glenohumeral joint (GHJ), leads to functional limitation, and reduces quality of life. Primary frozen shoulder occurs without any obvious connection to any other condition, and secondary frozen shoulder is related to some medical p…

NCT06807424 — A Study to Evaluate the Efficacy and Safety of Icotrokinra (JNJ-77242113) in Biologic-experienced and Biologic-naive Participants With Active Psoriatic Arthritis

StatusRecruiting
PhasePhase 3
SponsorJanssen Research & Development, LLC
Enrollment750
Study TypeINTERVENTIONAL
ConditionsArthritis, Psoriatic
Interventions;

The purpose of this study is to evaluate the efficacy of icotrokinra (JNJ-77242113) compared to placebo in biologic-experienced and biologic-naive participants with active psoriatic arthritis (PsA) by assessing the reduction in signs and symptoms of PsA.

NCT07688902 — Intralesional Versus Perilesional 5% Dextrose Injection in Partial Rotator Cuff Tears

StatusRecruiting
PhaseN/A
SponsorAnkara City Hospital Bilkent
Enrollment30
Study TypeINTERVENTIONAL
ConditionsPartial Rotator Cuff Tears; Rotator Cuff Tendinopathy; Shoulder Pain Chronic; Supraspinatus Tendon Tear
Interventions;

This prospective, randomized, double-blind controlled clinical trial aims to compare the clinical and ultrasonographic outcomes of intralesional and perilesional 5% dextrose injection in patients with partial rotator cuff tears. Eligible participants will be randomized into two parallel groups. Both groups will receive ultrasound-guided 5% dextrose injection to the supraspinatus enthesis. In ad…

StatusRecruiting
PhasePhase 3
SponsorUCB Biopharma SRL
Enrollment40
Study TypeINTERVENTIONAL
ConditionsEnthesitis-related Arthritis; Juvenile Psoriatic Arthritis
Interventions

The purpose of this study is to assess plasma bimekizumab concentrations following subcutaneous (sc) bimekizumab administration.

NCT06915363 — BioPoly® Partial Resurfacing Knee Implant IDE

StatusRecruiting
PhaseN/A
SponsorBioPoly LLC
Enrollment152
Study TypeINTERVENTIONAL
ConditionsKnee Pain Chronic; Knee Osteoarthritis; Cartilage Damage; Cartilage Defects of the Knee; Cartilage or Osteochondral Defects in the Knee
Interventions;

The goal of this randomized controlled clinical trial is to demonstrate the safety and effectiveness of the BioPoly® Partial Resurfacing Knee Implant for the treatment of cartilage defects of the distal femur in adult patients with knee pain and symptoms who are candidates for surgical intervention of the knee compared to outcomes for the control group.

The primary effectiveness endpoint is Mo…

NCT07153471 — A Study of Orforglipron (LY3502970) in Participants With Obesity or Overweight and Osteoarthritis (OA) of the Knee

StatusRecruiting
PhasePhase 3
SponsorEli Lilly and Company
Enrollment800
Study TypeINTERVENTIONAL
ConditionsOsteoarthritis
Interventions;

The GZPT master protocol will support two independent studies, J2A-MC-GZT1 and J2A-MC-GZT2. Each study will see how well and safely orforglipron works in people with obesity or overweight who have osteoarthritis (OA) of the knee with pain. Participation in the study will last about 74 weeks.

NCT07016672 — Efficacy of Therapy With PRP Injections Versus HA in Patients With Advanced Grade of GONArthrosis

StatusRecruiting
PhaseN/A
SponsorCentre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Enrollment150
Study TypeINTERVENTIONAL
ConditionsKnee Osteoarthritis
Interventions;

Gonarthrosis is a chronic pathology affecting the knee joint and tissues. It is characterized by progressive degeneration of articular cartilage, bone and surrounding structures. Diagnosis is based on clinical, biological and radiological criteria.

When knee osteoarthritis becomes symptomatic, it leads to pain associated with stiffness and functional discomfort, impacting on patients’ quality …

NCT07689461 — VR Effects After Hip Replacement Surgery Pain

StatusRecruiting
PhaseN/A
SponsorAdiyaman University
Enrollment80
Study TypeINTERVENTIONAL
ConditionsVirtual Reality; Hip Arthropathy; Comfort; Anxiety; Pain, Postoperative
Interventions

Total Hip Arthroplasty (THA), a procedure performed to enhance the quality of life, is accompanied by postoperative challenges such as pain and anxiety that adversely affect patient comfort. Inadequate management of these complications can prolong the length of hospital stay, delay recovery, lead to functional impairments, and elevate the risk of chronic pain development. Conventional pharmacol…

NCT07220824 — A Study of Guselkumab in Participants With Psoriatic Arthritis (PsA) in a Real-World Setting

StatusRecruiting
PhaseN/A
SponsorJanssen Research & Development, LLC
Enrollment200
Study TypeOBSERVATIONAL
ConditionsArthritis, Psoriatic

The purpose of this study is to assess how well guselkumab works in improving symptoms of psoriatic arthritis (an inflammatory disease that affects the joints in participants with psoriasis, a skin condition that causes red, scaly patches) using muscoloskeletal ultrasound (MSUS) in a real-world setting.

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…

NCT07353931 — Efficacy and Safety of Eloralintide (LY3841136) in Participants With Osteoarthritis Knee Pain and Obesity or Overweight

StatusRecruiting
PhasePhase 3
SponsorEli Lilly and Company
Enrollment900
Study TypeINTERVENTIONAL
ConditionsOsteoarthritis; Overweight or Obesity
Interventions;

The YDAN master protocol will support two independent studies, J3R-MC-YOA1 and J3R-MC-YOA2. Each study will investigate how well and safely Eloralintide (LY3841136) works in adults with obesity or overweight who have osteoarthritis (OA) of the knee with pain. Participation in the study will last about 75 weeks, including screening.

NCT07293871 — Ultrasound Neuroimmune Modulation in Adults With Rheumatoid Arthritis

StatusRecruiting
PhaseN/A
SponsorSurf Therapeutics
Enrollment40
Study TypeINTERVENTIONAL
ConditionsRheumatoid Arthritis
Interventions;

This two-stage, multicenter clinical trial is designed to evaluate the feasibility, safety, and preliminary efficacy of splenic ultrasound stimulation to activate immune-neuromodulation (SUSTAIN) in patients with rheumatoid arthritis (RA) and at least moderate disease activity. The findings from this trial will directly inform the design and power calculations for a future pivotal trial by iden…

Active, Not Recruiting

NCT04624256 — Germline DNA-Based Radiosensitivity Biomarker Influence on Toxicity Following Prostate Radiotherapy, GARUDA Trial

StatusActive, not recruiting
PhaseN/A
SponsorJonsson Comprehensive Cancer Center
Enrollment208
Study TypeINTERVENTIONAL
ConditionsProstate Adenocarcinoma; Stage I Prostate Cancer American Joint Committee on Cancer (AJCC) v8; Stage II Prostate Cancer AJCC v8; Stage IIA Prostate Cancer AJCC v8; Stage IIB Prostate Cancer AJCC v8
Interventions; ;

This trial studies the changes in long-term physician-scored genitourinary toxicity achieved in prostate cancer patients eligible for stereotactic radiation therapy when both patients and physicians have access to convincing but non-validated germline signature that can characterize patients as having a low or high risk of developing toxicity after radiation therapy. The information learned fro…

NCT04936308 — Guselkumab in Active Psoriatic Arthritis Participants With Inadequate Response/Intolerance to One Prior Anti-TNF Alpha Agent

StatusActive, not recruiting
PhasePhase 3
SponsorJanssen Research & Development, LLC
Enrollment453
Study TypeINTERVENTIONAL
ConditionsArthritis, Psoriatic
Interventions;

The purpose of this study is to evaluate the efficacy of guselkumab treatment in participants with active psoriatic arthritis (PsA) and inadequate response (IR) and/or intolerance to a prior anti-tumor necrosis factor (TNF) by assessing the reduction in signs and symptoms of PsA.

NCT05092269 — A Long-term Extension Study of Ustekinumab in Pediatric Participants

StatusActive, not recruiting
PhasePhase 3
SponsorJanssen Research & Development, LLC
Enrollment159
Study TypeINTERVENTIONAL
ConditionsCrohn Disease; Colitis, Ulcerative; Arthritis, Psoriatic
Interventions

The purpose of this study is to collect long-term safety data of subcutaneous (SC) ustekinumab

NCT05703178 — Web-based Pain Coping Skills Training for Breast Cancer Survivors With AI-Associated Arthralgia

StatusActive, not recruiting
PhasePhase 3
SponsorNorthwestern University
Enrollment452
Study TypeINTERVENTIONAL
ConditionsBreast Cancer; Arthralgia; Pain, Chronic
Interventions;

The main goal of this clinical trial is to test benefits of completing online pain coping skills training program in women who have been diagnosed with stage I-III breast cancer, who have completed their primary cancer treatment, who are taking an AI medication, and who have arthralgia. Arthralgia is a type of joint, bone, and muscle pain that is a common side effect of AI medications. The main…

NCT05772325 — The Effect of Brief Versus Individually Tailored Dietary Advice on Change in Lipids, Blood Pressure, and Diet in Patients With Inflammatory Joint Disease

StatusActive, not recruiting
PhaseN/A
SponsorDiakonhjemmet Hospital
Enrollment70
Study TypeINTERVENTIONAL
ConditionsRheumatoid Arthritis; Psoriatic Arthritis; Spondyloarthritis
Interventions;

A randomized controlled study comparing brief dietary intervention with a personal, tailored dietary advice (60 min) on change in LDL-c and change in diet.

NCT05985915 — A Randomized, Double-blind 2-arm, Followed by an Open-label 1-arm, NEPTUNUS Extension Study to Assess the Long-term Safety and Efficacy of Ianalumab in Patients With Sjogrens Syndrome.

StatusActive, not recruiting
PhasePhase 3
SponsorNovartis Pharmaceuticals
Enrollment612
Study TypeINTERVENTIONAL
ConditionsSjogrens Syndrome
Interventions;

The purpose of this study is to measure the long-term safety and tolerability of ianalumab in participants with Sjögren’s syndrome who have previously completed treatment from one of two NEPTUNUS 1 year core studies (CVAY736A2301 [NCT05350072] or CVAY736A2302 [NCT05349214]).

NCT06001853 — Allogeneic BM-MSCs in Patients With Painful Lumbar Facet Arthropathy

StatusActive, not recruiting
PhasePhase 2
SponsorMayo Clinic
Enrollment40
Study TypeINTERVENTIONAL
ConditionsFacet-Mediated Low Back Pain; Lumbar Facet Joint Osteoarthritis
Interventions;

The purpose of this research study is to evaluate the safety and effect of bone marrow-derived stem cells for the treatment of low back pain.

NCT06741969 — Nipocalimab in Moderate to Severe Sjogren’s Disease

StatusActive, not recruiting
PhasePhase 3
SponsorJanssen Research & Development, LLC
Enrollment655
Study TypeINTERVENTIONAL
ConditionsSjogrens Syndrome
Interventions; ;

The purpose of this study is to evaluate the clinical efficacy and safety of nipocalimab in participants with moderate to severe Sjogren’s disease (SjD).

NCT07688174 — The REFLECT Study- Flares in axSpA

StatusActive, not recruiting
PhaseN/A
SponsorRoyal United Hospitals Bath NHS Foundation Trust
Enrollment40
Study TypeOBSERVATIONAL
ConditionsAxial Spondyloarthritis (AxSpA); Axial Spondyloarthritis, Non-Radiographic; Axial Spondyloarthritis, Radiographic; Axial Spondylarthritis (r-axSpA)

Axial spondyloarthritis (axSpA) is a long-term inflammatory condition that affects the spine and sacroiliac joints. People living with axSpA often experience periods when their symptoms suddenly worsen, known as disease “flares.” These flares can be painful, unpredictable, and significantly affect daily life, work and psychological wellbeing. Their unpredictable nature can leave people feeling …

Not Yet Recruiting

NCT07688642 — Circulatory Exercise After Total Knee Replacement

StatusNot yet recruiting
PhaseN/A
SponsorAssiut University
Enrollment68
Study TypeINTERVENTIONAL
ConditionsTotal Knee Replacement; Knee Osteoarthritis; Postoperative Edema; Postoperative Inflammation
Interventions;

Total knee replacement is commonly associated with early postoperative inflammation, edema, pain, and reduced mobility. This randomized controlled trial will evaluate whether adding a simple circulatory exercise program to standard postoperative rehabilitation reduces early limb edema and inflammatory response after unilateral primary total knee replacement. Participants will be randomized to s…

NCT07522489 — Imageless Navigation Versus Image-Based Navigation in Robotic-Assisted Total Knee Arthroplasty for Knee Osteoarthritis

StatusNot yet recruiting
PhaseN/A
SponsorMedical University of Warsaw
Enrollment146
Study TypeINTERVENTIONAL
ConditionsOsteoarthritis (OA) of the Knee; Knee Pain Arthritis; Total Knee Arthroplasty (TKA); Robotic Assisted Arthroplasty
Interventions;

The goal of this clinical trial is to learn if imageless navigation is not inferior to image-based navigation in robotic-assisted total knee arthroplasty (RA-TKA) for treating patients with knee osteoarthritis.

The main questions the study aims to answer are:

  1. Does imageless procedure provide functional results comparable to those of image-based navigation?
  2. Are there differences in posto…

NCT07688096 — Regenerative Medicine for Joint Hypermobility and Instability

StatusNot yet recruiting
PhasePhase 1 / Phase 2
SponsorManhattan Pain Medicine, PLLC
Enrollment100
Study TypeINTERVENTIONAL
ConditionsEhlers-Danlos Syndrome Hypermobility Type (hEDS); Ehlers-Danlos Syndrome (EDS); Joint Hypermobility; Joint Instability; Hypermobility Spectrum Disorder
Interventions; ;

This clinical trial is designed to evaluate whether a stepwise injection-based treatment approach can reduce pain and improve function in adults with joint hypermobility, connective tissue laxity, and joint instability.

Joint hypermobility occurs when joints move beyond their normal range, often because of looser connective tissue. For some patients, this can contribute to chronic pain, recurr…

NCT07288411 — Effects of Vagus Nerve Stimulation on Temporomandibular Disorders.

StatusNot yet recruiting
PhaseN/A
SponsorArpana Church
Enrollment10
Study TypeINTERVENTIONAL
ConditionsTMD; Temporomandibular Disorders (TMDs)
Interventions

The study aims to examine the effects of transcutaneous non-invasive vagus nerve stimulation (nVNS) on symptoms and brain mechanisms in premenopausal women with temporomandibular disorders (TMD). Non-invasive vagus nerve stimulation (nVNS) is the most well researched and possibly the most effective non-invasive neuromodulation treatment for chronic pain conditions that targets the brain-gut-mic…

NCT07685743 — Extended Post-operative Oral TXA in Primary THA

StatusNot yet recruiting
PhasePhase 4
SponsorOregon Health and Science University
Enrollment170
Study TypeINTERVENTIONAL
ConditionsOsteoarthritis (OA) of the Hip; Osteoarthritis (OA) of the Knee
Interventions;

The goal of this clinical trial is to learn if extended post-operative oral tranexamic acid (TXA) - a medication that reduces bleeding by slowing the breakdown of blood clots - can improve functional recovery following surgery in adults undergoing primary total knee or hip arthroplasty for osteoarthritis. The main question it aims to answer is: Does extended post-operative oral TXA improve func…

NCT07563803 — The restor3d Outcomes Registry

StatusNot yet recruiting
PhaseN/A
SponsorRestor3D
Enrollment2000
Study TypeOBSERVATIONAL
ConditionsJoint Replacement; Arthropathy
Interventions

The restor3d Outcomes Registry is a prospective, longitudinal, decentralized study designed to capture patient-reported outcomes (PROs) from adults who have received an FDA-cleared or approved restor3d patient-specific orthopedic implant. Using a master protocol framework, the study enrolls patients across multiple joint cohorts (knee, hip, foot & ankle, shoulder) under a single protocol, with…

NCT07189585 — Inulin Supplementation for Reducing Inflammation and Knee Pain in Older Adults With Osteoarthritis

StatusNot yet recruiting
PhasePhase 2
SponsorYale University
Enrollment84
Study TypeINTERVENTIONAL
ConditionsKnee Osteoarthritis
Interventions;

This study will test whether inulin, a type of dietary fiber, can reduce inflammation in older adults with knee osteoarthritis. Inflammation in the body may contribute to both joint pain and the progression of osteoarthritis. Inulin is a prebiotic fiber that may improve gut health and reduce lipopolysaccharide (LPS), a marker of bacterial products in the blood that is linked to inflammation.

I…

Enrolling by Invitation

NCT07286513 — Persona SoluTion PPS Femur PMCF

StatusEnrolling by invitation
PhaseN/A
SponsorZimmer Biomet
Enrollment200
Study TypeOBSERVATIONAL
ConditionsRhematoid Arthritis; Osteo Arthritis of the Knee; Traumatic Arthritis of Knee (Diagnosis); Polyarthritis; Collagen Disorders
Interventions

The goal of this study is to generate clinical evidence and evaluate the safety and performance of the Persona® SoluTion® PPS Femurs in the US market, with data supporting global regulatory submissions, including CE marking under EU MDR.

The target population consists of adults undergoing knee arthroplasty with the Persona SoluTion femoral component paired with a Medial Congruent (MC) or Poste…

Completed Trials

NCT01862731 — Muscle Strength Loss and Its Effect on Knee Cap Motion in Volunteers With Anterior Knee Pain

StatusCompleted
PhaseN/A
SponsorNational Institutes of Health Clinical Center (CC)
Enrollment35
Study TypeOBSERVATIONAL
ConditionsPatellofemoral Pain Syndrome

Background:

- Researchers are interested in how the muscles affect the movement of the knee cap. These muscles may be related to different kinds of knee pain that are not caused by an injury or a disease. Imaging studies such as magnetic resonance imaging (MRI) can be used to look at these muscles. To study these muscles and how they move, researchers will use MRI to look at healthy individua…

NCT07688226 — Effect of Therapeutic Ultrasound Combined With Exercise on Subacromial Impingement Syndrome

StatusCompleted
PhaseN/A
SponsorUniversity of Sao Paulo General Hospital
Enrollment120
Study TypeINTERVENTIONAL
ConditionsShoulder Impingement Syndromes
Interventions; ;

The aim of this study is to analyze the effects of Therapeutic Ultrasound combined with a Therapeutic Exercises program on pain reduction and improvement of function, range of motion (ROM), and functionality in individuals with Subacromial Impingement Syndrome. The main questions it aims to answer are:

Can the application of therapeutic ultrasound combined with exercise reduce pain and improve…

NCT04196868 — Methotrexate and Metformin in Rheumatoid Arthritis Patients

StatusCompleted
PhasePhase 2
SponsorUniversity Hospital, Bordeaux
Enrollment128
Study TypeINTERVENTIONAL
ConditionsArthritis, Rheumatoid
Interventions; ;

Methotrexate (MTX) is the anchor drug for patients with rheumatoid arthritis (RA). Despite its marked efficacy and acceptable side effect profile, about 1/3 of patients failed to reach RA remission. Metformin is the first-line therapy for type 2 diabetes. Its antioxidative and anti-inflammatory properties make it a good candidate for the treatment of inflammatory diseases such as rheumatoid art…

NCT05027581 — Chondrochymal® for Subjects With Knee Osteoarthritis (Knee OA)

StatusCompleted
PhasePhase 2
SponsorTaiwan Bio Therapeutics Inc.
Enrollment72
Study TypeINTERVENTIONAL
ConditionsOsteoarthritis, Knee
Interventions;

This is a randomized, single-blind, parallel, active-controlled study to evaluate the efficacy and safety of bone marrow mesenchymal stem cells (BM-MSCs), Chondrochymal®, in subjects aged 40 to 80 with knee OA.

NCT03291470 — Study to Determine the Efficacy and Safety of TG-C in Subjects With Kellgren/Lawrence Grade 2 or 3 OA of the Knee

StatusCompleted
PhasePhase 3
SponsorKolon TissueGene, Inc.
Enrollment531
Study TypeINTERVENTIONAL
ConditionsDegenerative Osteoarthritis
Interventions;

A randomized, double-blind, placebo-controlled, multi-center, phase 3 study to determine the efficacy and safety of TG-C in subjects with Kellgren and Lawrence Grade 2 or 3 Osteoarthritis of the Knee, Osteoarthritis Research Society International (OARSI) medial joint space narrowing (JSN) Grade 1 or 2 of the knee joint. TG-C is to be administered by a single intra-articular injection to the dam…

NCT05350072 — Two-arm Study to Assess Efficacy and Safety of Ianalumab (VAY736) in Patients With Active Sjogren’s Syndrome

StatusCompleted
PhasePhase 3
SponsorNovartis Pharmaceuticals
Enrollment275
Study TypeINTERVENTIONAL
ConditionsSjogren Syndrome
Interventions;

A randomized, double-blind, placebo controlled, 2-arm multicenter phase 3 study to assess the efficacy and safety of ianalumab in patients with active Sjogren’s syndrome (NEPTUNUS-1)

NCT05530551 — Effect of Single vs Multiple Prophylactic Antibiotic Doses on PJI Following Primary THA in Patients With OA

StatusCompleted
PhaseN/A
SponsorSoren Overgaard
Enrollment20000
Study TypeINTERVENTIONAL
ConditionsOsteoarthritis, Hip; Total Hip Arthroplasty; Prosthetic-joint Infection
Interventions

Aim: To compare the effect of one single dose versus multiple doses of prophylactic antibiotics administered within 24 hours, on the development of PJI in patients with osteoarthritis undergoing primary THA.

The study is designed as a cross-over, cluster randomized, non-inferiority trial. All Danish orthopedic surgery departments performing primary THA with the majority being within inclusion …

NCT07687927 — Fixed Versus Conventional Twin Block Appliances for Skeletal Class II Malocclusion

StatusCompleted
PhaseN/A
SponsorAl-Azhar University
Enrollment20
Study TypeINTERVENTIONAL
ConditionsSkeletal Class II Malocclusion; Mandibular Retrognathia
Interventions

This study compares two types of dental appliances a fixed Twin Block appliance and a conventional (removable) Twin Block appliance used to treat a bite problem called skeletal Class II malocclusion in growing children and teenagers. In this condition, the lower jaw is positioned further back than the upper jaw. Both appliance types work by guiding the lower jaw forward during growth. The study…

NCT06288867 — A 12 Months Prospective Study Comparing Functional Outcome Scores in Hip Arthroscopic Labral Repair Versus Debridement

StatusCompleted
PhaseN/A
SponsorAin Shams University
Enrollment60
Study TypeINTERVENTIONAL
ConditionsHip Injuries; Acetabular Labral Tear; Femoro Acetabular Impingement
Interventions;

This study aims to address hip labral tears and compare between arthroscopic labral repair versus debridement in non non-athletic population aged 20 to 40 years old, including both sexes.

NCT05706493 — Association Between Periodontitis and the Level of Anti-citrullinated Protein Antibodies in Rheumatoid Arthritis

StatusCompleted
PhaseN/A
SponsorMisr International University
Enrollment62
Study TypeOBSERVATIONAL
ConditionsPeriodontal Diseases; Rheumatoid Arthritis

the relationship between rheumatoid arthritis and periodontal disease is crucial and has been explained via a complex interplay of genetic, environmental, and hormonal factors that influence the host immune tolerance leading to both disease characteristics. The aim of this study is to clinically investigate the correlation between the levels of anti-citrullinated protein antibodies (ACPAs) in g…

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…

NCT06336252 — Technology Assisted Nudging to Increase Physical Activity Among Hospitalised Medical Patients

StatusCompleted
PhaseN/A
SponsorBispebjerg Hospital
Enrollment130
Study TypeINTERVENTIONAL
ConditionsCOPD; Heart Failure; Parkinson Disease; Arthritis; Old Age; Cachexia
Interventions

Primary Objective To investigate if patients hospitalised for older adults with a decreased level of physical function, either related to a chronic condition e.g., COPD, Congestive heart failure, renal failure; infections; frailty and tendency of falling; orthopaedic surgery - after hip fracture will increase their time spent out of bed during hospitalisation and 3 months after discharge throug…

NCT06626568 — Comparison of Ultrasound-Guided Subacromial vs. Systemic Steroid Injections for Frozen Shoulder: a Multicenter Pilot Study

StatusCompleted
PhasePhase 2
SponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University
Enrollment40
Study TypeINTERVENTIONAL
ConditionsFrozen Shoulder
Interventions; ;

The goal of this multicenter pilot study is to validate the effectiveness of extending the injection interval between betamethasone doses from one to two weeks for treating frozen shoulder (adhesive capsulitis) in adults aged 18 to 75. This study also aims to screen potential study centers and gather data to refine the sample size calculation for a larger, future trial. The main questions it ai…

NCT06869200 — Study on the Use of a Concentrated Growth Factor Preparation Kit for the Treatment of Knee Osteoarthritis

StatusCompleted
PhaseN/A
SponsorGuangdong Hongzhi Health Technology
Enrollment104
Study TypeINTERVENTIONAL
ConditionsKnee Osteoarthritis
Interventions;

The goal of this clinical trial is to evaluate the effectiveness and safety of an autologous platelet-rich concentrated growth factor (CGF) preparation kit for the treatment of knee osteoarthritis in patients diagnosed with this condition. The main question it aims to answer is:

Can the CGF preparation kit effectively improve symptoms and reduce pain in patients with knee osteoarthritis compar…

NCT05475639 — Axillary Phonophoresis Versus Post Isometric Facilitation in the Treatment of Shoulder Adhesive Capsulitis

StatusCompleted
PhaseN/A
SponsorCairo University
Enrollment45
Study TypeINTERVENTIONAL
ConditionsAdhesive Capsulitis of Shoulder
Interventions; ;

the aim of this study is to compare the effect of Axillary Phonophoresis versus Post isometric facilitation in subjects with Adhesive capsulitis

NCT07689916 — Machine Learning-Based Risk Identification and Precision Exercise for Common Running Injuries

StatusCompleted
PhaseN/A
SponsorZeyi Zhang
Enrollment204
Study TypeINTERVENTIONAL
ConditionsRunning-related Injuries; Medial Tibial Stress Syndrome; Patellofemoral Pain, PFP; Chronic Achilles Tendinopathy
Interventions;

This study aims to identify biomechanical risk factors associated with common running-related injuries in recreational runners using machine learning analysis. It also aims to evaluate whether a precision exercise intervention based on these risk factors can improve injury-related biomechanical and kinematic outcomes.

The main questions it aims to answer are:

Which biomechanical features iden…

NCT07639918 — Effect of Kinesio-taping With Routine Physical Therapy in Wrist Joint Hypermobility

StatusCompleted
PhaseN/A
SponsorUniversity of Lahore
Enrollment38
Study TypeINTERVENTIONAL
ConditionsWrist Joint Hypermobility
Interventions;

The study will be randomized controlled trial. This study will be conducted at the University of Lahore Teaching Hospital, Lahore, Pakistan. This will investigate the effects of routine physical therapy with and without Kinesio taping in patients with Wrist Joint Hypermobility. A sample size of 38 participants will be randomly assigned into two groups. Group A will receive routine physical ther…