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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) |
| Enrollment | 7500 |
| Study Type | OBSERVATIONAL |
| Conditions | Rheumatic 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institutes of Health Clinical Center (CC) |
| Enrollment | 750 |
| Study Type | OBSERVATIONAL |
| Conditions | Abnormalities; 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) |
| Enrollment | 2000 |
| Study Type | OBSERVATIONAL |
| Conditions | Arthritis; 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)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Maryland, Baltimore |
| Enrollment | 78 |
| Study Type | INTERVENTIONAL |
| Conditions | Pain; 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Shin Kong Wu Ho-Su Memorial Hospital |
| Enrollment | 94 |
| Study Type | INTERVENTIONAL |
| Conditions | Frozen 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
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Janssen Research & Development, LLC |
| Enrollment | 750 |
| Study Type | INTERVENTIONAL |
| Conditions | Arthritis, 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Ankara City Hospital Bilkent |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Partial 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…
NCT06668181 — An Open-label Study to Evaluate the Pharmacokinetics and Safety of Bimekizumab in Pediatric Study Participants With Active Juvenile Idiopathic Arthritis Subtypes Enthesitis-related Arthritis (Including Juvenile-onset Ankylosing Spondylitis) and Juvenile Psoriatic Arthritis
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | UCB Biopharma SRL |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Enthesitis-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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | BioPoly LLC |
| Enrollment | 152 |
| Study Type | INTERVENTIONAL |
| Conditions | Knee 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
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 800 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoarthritis |
| 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer |
| Enrollment | 150 |
| Study Type | INTERVENTIONAL |
| Conditions | Knee 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Adiyaman University |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Virtual 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Janssen Research & Development, LLC |
| Enrollment | 200 |
| Study Type | OBSERVATIONAL |
| Conditions | Arthritis, 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
| 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…
NCT07353931 — Efficacy and Safety of Eloralintide (LY3841136) in Participants With Osteoarthritis Knee Pain and Obesity or Overweight
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 900 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoarthritis; 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Surf Therapeutics |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatoid 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
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Jonsson Comprehensive Cancer Center |
| Enrollment | 208 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate 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
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Janssen Research & Development, LLC |
| Enrollment | 453 |
| Study Type | INTERVENTIONAL |
| Conditions | Arthritis, 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
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Janssen Research & Development, LLC |
| Enrollment | 159 |
| Study Type | INTERVENTIONAL |
| Conditions | Crohn 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
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Northwestern University |
| Enrollment | 452 |
| Study Type | INTERVENTIONAL |
| Conditions | Breast 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
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Diakonhjemmet Hospital |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatoid 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.
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 612 |
| Study Type | INTERVENTIONAL |
| Conditions | Sjogrens 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
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Mayo Clinic |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Facet-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
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Janssen Research & Development, LLC |
| Enrollment | 655 |
| Study Type | INTERVENTIONAL |
| Conditions | Sjogrens 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
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Royal United Hospitals Bath NHS Foundation Trust |
| Enrollment | 40 |
| Study Type | OBSERVATIONAL |
| Conditions | Axial 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
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Assiut University |
| Enrollment | 68 |
| Study Type | INTERVENTIONAL |
| Conditions | Total 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
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Medical University of Warsaw |
| Enrollment | 146 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoarthritis (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:
- Does imageless procedure provide functional results comparable to those of image-based navigation?
- Are there differences in posto…
NCT07688096 — Regenerative Medicine for Joint Hypermobility and Instability
| Status | Not yet recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Manhattan Pain Medicine, PLLC |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Ehlers-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.
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Arpana Church |
| Enrollment | 10 |
| Study Type | INTERVENTIONAL |
| Conditions | TMD; 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
| Status | Not yet recruiting |
| Phase | Phase 4 |
| Sponsor | Oregon Health and Science University |
| Enrollment | 170 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoarthritis (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
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Restor3D |
| Enrollment | 2000 |
| Study Type | OBSERVATIONAL |
| Conditions | Joint 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
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | Yale University |
| Enrollment | 84 |
| Study Type | INTERVENTIONAL |
| Conditions | Knee 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
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | Zimmer Biomet |
| Enrollment | 200 |
| Study Type | OBSERVATIONAL |
| Conditions | Rhematoid 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
| Status | Completed |
| Phase | N/A |
| Sponsor | National Institutes of Health Clinical Center (CC) |
| Enrollment | 35 |
| Study Type | OBSERVATIONAL |
| Conditions | Patellofemoral 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
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Sao Paulo General Hospital |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Shoulder 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
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | University Hospital, Bordeaux |
| Enrollment | 128 |
| Study Type | INTERVENTIONAL |
| Conditions | Arthritis, 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)
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Taiwan Bio Therapeutics Inc. |
| Enrollment | 72 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoarthritis, 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
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | Kolon TissueGene, Inc. |
| Enrollment | 531 |
| Study Type | INTERVENTIONAL |
| Conditions | Degenerative 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
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 275 |
| Study Type | INTERVENTIONAL |
| Conditions | Sjogren 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Soren Overgaard |
| Enrollment | 20000 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoarthritis, 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Al-Azhar University |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Skeletal 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Ain Shams University |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Hip 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Misr International University |
| Enrollment | 62 |
| Study Type | OBSERVATIONAL |
| Conditions | Periodontal 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…
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…
NCT06336252 — Technology Assisted Nudging to Increase Physical Activity Among Hospitalised Medical Patients
| Status | Completed |
| Phase | N/A |
| Sponsor | Bispebjerg Hospital |
| Enrollment | 130 |
| Study Type | INTERVENTIONAL |
| Conditions | COPD; 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
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Second Affiliated Hospital, School of Medicine, Zhejiang University |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Frozen 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Guangdong Hongzhi Health Technology |
| Enrollment | 104 |
| Study Type | INTERVENTIONAL |
| Conditions | Knee 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Cairo University |
| Enrollment | 45 |
| Study Type | INTERVENTIONAL |
| Conditions | Adhesive 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Zeyi Zhang |
| Enrollment | 204 |
| Study Type | INTERVENTIONAL |
| Conditions | Running-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
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Lahore |
| Enrollment | 38 |
| Study Type | INTERVENTIONAL |
| Conditions | Wrist 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…