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 Infectious Arthritis from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 22
- Active, not recruiting: 2
- Completed: 10
- Other: 16
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT04402086 — Rheumatology Patient Registry and Biorepository
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Yale University |
| Enrollment | 5000 |
| Study Type | OBSERVATIONAL |
| Conditions | Rheumatic Diseases; Adult Onset Still Disease; Ankylosing Spondylitis; Psoriatic Arthritis; Reactive Arthritis |
To facilitate clinical, basic science, and translational research projects involving the study of rheumatic diseases.
NCT04538053 — BonE and Joint Infections - Simplifying Treatment in Children Trial
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Murdoch Childrens Research Institute |
| Enrollment | 285 |
| Study Type | INTERVENTIONAL |
| Conditions | Bone Infection; Septic Arthritis; Bone and Joint Infection; Osteomyelitis |
| Interventions | ; |
This is a multi- centre trial of children with bone and joint infections (BJIs) at eight major paediatric hospitals in Australia and New Zealand. The primary objective is to establish if in children with acute, uncomplicated BJIs, entirely oral antibiotic treatment is not inferior to initial intravenous (IV) treatment for 1 to 7 days followed by an oral antibiotic course in achieving full recov…
NCT04821154 — Persona Revision Knee System Outcomes
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Zimmer Biomet |
| Enrollment | 380 |
| Study Type | OBSERVATIONAL |
| Conditions | Arthroplasty Complications; Infection; Knee Disease; Knee Osteoarthritis |
| Interventions |
The study will evaluate the performance, clinical benefits and safety of the Persona Revision Knee System in patients who have received primary or revision total knee arthroplasty (TKA) treatment. This will be done using a multicenter, single-arm, consecutive series, retrospective cohort study with prospective follow-up.
NCT04536103 — Multi-Vendor Multi-Site Novel Accelerated MRI Relaxometry
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Xiaojuan Li |
| Enrollment | 88 |
| Study Type | OBSERVATIONAL |
| Conditions | Bone Diseases, Infectious; Musculoskeletal Diseases; Joint Diseases; Osteoarthritis; ACL Tear |
| Interventions |
Currently the diagnosis of OA is based on radiographs and clinical findings, which is limited to detecting late-stage disease. There is a pressing, unmet clinical need for robust assessment of early changes in cartilage health. Towards this goal, extensive efforts are ongoing to develop quantitative MRI for cartilage matrix analysis. MR T1ρ and T2 relaxation times have shown to be promising ima…
NCT05169229 — Antibiotic Impregnated Bone Graft to Reduce Infection in Hip Replacement.
| Status | Recruiting |
| Phase | Phase 2 / Phase 3 |
| Sponsor | University Hospital, Linkoeping |
| Enrollment | 1100 |
| Study Type | INTERVENTIONAL |
| Conditions | Arthroplasty, Replacement, Hip; Osteoarthritis, Hip; Antibiotic Resistant Infection; Prosthetic Joint Infection |
| Interventions | ; |
Total hip replacement is the most successful treatment modern healthcare can offer patients to regain quality of life. Periprosthetic joint infection (PJI) is the most common and devastating complication after total hip replacement (THR). Between 0.5 to 2% of primary THR (first time hip replacement), and 8-10% of revision THR (replacement of a hip prosthesis) will become infected.1 The introduc…
NCT04751396 — Testing of an Educational Tool for Patients With Melanoma and Pre-Existing Autoimmune Disease Who Are Candidates for Immune Checkpoint Inhibitors
| Status | Recruiting |
| Phase | N/A |
| Sponsor | M.D. Anderson Cancer Center |
| Enrollment | 125 |
| Study Type | OBSERVATIONAL |
| Conditions | Ankylosing Spondylitis; Autoimmune Disease; Crohn Disease; Enteropathic Arthritis; Enteropathic Spondylitis |
| Interventions | ; ; |
This study learn how easily patients can use an educational tool that will be created for patients with melanoma and pre-existing autoimmune diseases who receive or will receive immune checkpoint inhibitor drugs. Patients will be asked their opinions about the design, accessibility, and content of the tool. Researchers will use the information collected to improve the educational materials that…
NCT05543941 — Evaluating XPERIENCE™ Advanced Surgical Irrigation
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Ottawa Hospital Research Institute |
| Enrollment | 7600 |
| Study Type | INTERVENTIONAL |
| Conditions | Hip Osteoarthritis; Hip Arthritis; Knee Osteoarthritis; Knee Arthritis |
| Interventions | ; |
A prospective, multi-center, double-arm, parallel, interventional, randomized, controlled clinical trial to assess the rate of periprosthetic joint infection (PJI) in patients undergoing primary total knee arthroplasty (TKA), total hip arthroplasty (THA) or hip resurfacing (HR) with XPERIENCE™ (XP) Advanced Surgical Irrigation versus dilute Betadine (DB).
NCT04806620 — Unhide® Project: A Digital Health Platform to Collect Lifestyle Data for Brain Inflammation Research
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Brain Inflammation Collaborative |
| Enrollment | 10000 |
| Study Type | OBSERVATIONAL |
| Conditions | Post-Acute COVID-19 Syndrome; ME/CFS; Rheumatic Arthritis; Juvenile Rheumatoid Arthritis (JRA); Psoriatic Arthritis (PsA) |
The unhide® Project is a non-interventional, longitudinal research study designed to establish a secure data repository of demographic, health, and lifestyle information from individuals with brain inflammation and related neuroinflammatory conditions. Participants in the United States aged 2 years and older will provide self-reported health data, biometrics, and symptom diaries through the MyD…
NCT07065747 — Quantification & Classification of Inflammatory Cells in Uveitis Using OCT
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Oregon Health and Science University |
| Enrollment | 125 |
| Study Type | OBSERVATIONAL |
| Conditions | Anterior Uveitis (AU); Birdshot Chorioretinitis; Behcet Disease; Herpes Simplex Virus; Juvenile Idiopathic Arthritis (JIA) |
The goal of this study is to determine if it’s possible to use a high resolution imaging device called optical coherence tomography (OCT) to develop an unbiased, standard method of counting and categorizing the various types of cells and proteins found in an eye condition called anterior uveitis. Anterior uveitis is a type of inflammation in the eye that can be caused by many different diseases…
NCT06967883 — Ultrasound Assessment of Neck Muscles and Balance in Male Patients With Ankylosing Spondylitis
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Istanbul Physical Medicine Rehabilitation Training and Research Hospital |
| Enrollment | 76 |
| Study Type | OBSERVATIONAL |
| Conditions | Ankylosing Spondylitis; Balance Assessment; Balance; Spondylarthropathies; Spondylitis, Ankylosing |
| Interventions |
The aim of this study is to evaluate the relationship between ultrasonographic measurements of the cervical muscles and balance parameters in patients diagnosed with ankylosing spondylitis (AS)
NCT07388017 — Infrared Thermography for Diagnosis of Musculoskeletal Infections
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Sheffield Children’s NHS Foundation Trust |
| Enrollment | 30 |
| Study Type | OBSERVATIONAL |
| Conditions | Musculoskeletal Infection; Septic Arthritis; Osteomyelitis/Septic Arthritis |
| Interventions |
This is a pilot proof of feasibility study to explore the efficacy of High Resolution Infrared Thermographic Imaging (HRTI) to assist with the detection of musculoskeletal infections in children. In HRTI, a sensitive thermal camera is used to capture the temperature profile of the suspected infected body region in the form of images. In this study, a 10-second video will be recorded to allow dy…
NCT06946641 — A Phase I Study of QLS12010 Capsules: Safety, Tolerability, PK, PD, and Food Effects in Healthy Adults and Moderate to Severe Atopic Dermatitis Patients
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Shanghai Qilu Pharmaceutical Research and Development Center LTD |
| Enrollment | 102 |
| Study Type | INTERVENTIONAL |
| Conditions | Atopic Dermatitis; Hidradenitis Suppurativa (HS); Rheumatoid Arthritis (RA) |
| Interventions | ; |
The goal of this clinical trial is to evaluate the safety, tolerability, PK, and PD of single and multiple ascending doses of QLS12010 Capsules and the effect of food on their PK profiles in healthy adult participants and participants with atopic dermatitis. This study consists of four parts: Part A is a single ascending dose (SAD) study, once sufficient safety and PK data are obtained from the…
NCT07086989 — Cardiovascular Risk in Children With Chronic Conditions Study
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Semmelweis University |
| Enrollment | 300 |
| Study Type | OBSERVATIONAL |
| Conditions | Kidney Transplant; Familial Hypercholesterolaemia; Type 1 Diabetes Mellitus (T1DM); Type 2 Diabetes Mellitus (T2DM); Chronic Kidney Disease |
Children living with chronic health conditions face a higher risk of developing cardiovascular diseases than their peers, largely due to the accelerated aging of the heart and blood vessels. Although experts recognize this elevated risk and recommend close monitoring and early intervention, the underlying mechanisms driving this phenomenon remain poorly understood. At present, no effective inte…
NCT06982105 — Trimethoprim-sulfamethoxazole vs. Clindamycin for the Treatment of Children With Invasive MRSA Infections
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Indiana University |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Methicillin Resistant Staphylococcus Aureus; Osteomyelitis Acute; Septic Arthritis; Orbital Cellulitis; Facial Cellulitis |
| Interventions |
The goal of this clinical trial is to learn if trimethoprim-sulfamethoxazole (TMP-SMX) works to treat invasive infections due to methicillin-resistant Staphylococcus aureus (MRSA) in children. It will also learn about the safety of TMP-SMX in the treatment of children with invasive MRSA infections. The main questions it aims to answer are:
-Is TMP-SMX effective at successfully treating childre…
NCT07651462 — Preoperative Fasting and the Gut Microbiome Before Hip Replacement
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Charite University, Berlin, Germany |
| Enrollment | 130 |
| Study Type | INTERVENTIONAL |
| Conditions | Hip Osteoarthritis; Arthroplasty, Replacement, Hip; Postoperative Complications; Surgical Wound Infection; Gastrointestinal Microbiome |
| Interventions |
Postoperative complications occur in 5-15% of patients undergoing elective primary total hip arthroplasty (THA), including periprosthetic joint infection (PJI), thrombosis, wound healing disorders, and metabolic dysregulation. The gut microbiome and the systemic immune profile have both been implicated as modifiable contributors to perioperative complication risk. Preoperative therapeutic fasti…
NCT07123038 — A Long-Term Follow-Up Observational Study to Evaluate Safety in Subjects Who Have Received a Gene-Modified Regulatory T Cell (Treg) Therapeutic
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Sonoma Biotherapeutics, Inc. |
| Enrollment | 36 |
| Study Type | OBSERVATIONAL |
| Conditions | Rheumatoid Arthritis (RA); Hidradenitis Suppurativa (HS) |
| Interventions |
To assess the emergence, type, severity, and potential causality of delayed adverse events following administration of a gene-modified Treg therapeutic.
NCT07284563 — Ultralow Dose PET Imaging for 18F-NaF Uptake
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Akiva Mintz |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Healthy Volunteer; Bone Alteration; Bone and Joint Cancer; Bone and Joint Infection; Arthritis |
| Interventions |
The goal of this clinical trial is to evaluate an investigational ultralow dose positron emission tomography (PET imaging) technique for increased bone turnover that is found in diseases such as cancer, trauma, infection, arthritis, and other benign diseases of bone detection and monitoring. The main question it aims to answer is:
Can the investigators optimize the timing, scan duration, and i…
NCT07439575 — Wound Closure Materials and Techniques in Hip and Knee Arthroplasty
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Bahattin Kemah |
| Enrollment | 90 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoarthritis, Knee; Osteoarthritis, Hip |
| Interventions | ; |
This prospective randomized clinical study aims to evaluate the effects of different suture materials and wound closure techniques on wound healing, functional outcomes, and postoperative complications in patients undergoing total hip and knee arthroplasty.
A total of at least 90 adult patients undergoing primary or aseptic revision lower extremity arthroplasty will be randomized into two grou…
NCT06888193 — A Study to Assess the Concentration of Bimekizumab in Mature Breast Milk From Mothers Receiving Treatment With Bimzelx® (Bimekizumab)
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | UCB Biopharma SRL |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Moderate to Severe Plaque Psoriasis; Psoriatic Arthritis; Axial Spondyloarthritis; Hidradenitis Suppurativa |
| Interventions |
Primary purpose of the study is to assess the concentration of bimekizumab in mature human breast milk.
NCT06718569 — Pain in Inflammatory Joint Diseases
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Diakonhjemmet Hospital |
| Enrollment | 350 |
| Study Type | OBSERVATIONAL |
| Conditions | Arthritis; Arthritis, Juvenile Idiopathic; Arthritis,Rheumatoid; Arthritis, Reactive; Arthritis, Psoriatic |
| Interventions |
Our primary objective is to better understand the etiology and consequences of chronic paint by using an explorative approach to identify phenotypes and endotypes of patients with inflammatory joint diseases, with a special focus on central sensitization and cognitive functioning as a key element in chronic pain. We will also examine the risk factors and clinical impact of these factors on pain…
NCT07243782 — Regulatory Post-Marketing Surveillance in Hidradenitis Suppurativa, Pediatric Plaque Psoriasis and JIA Treated With Cosentyx®(Secukinumab) in Korea
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 76 |
| Study Type | OBSERVATIONAL |
| Conditions | Hidradenitis Suppurativa; Pediatric Plaque Psoriasis; Juvenile Idiopathic Arthritis |
| Interventions |
Regulatory Post-Marketing Surveillance in hidradenitis suppurativa, pediatric plaque psoriasis and JIA treated with Cosentyx®(secukinumab) in Korea
NCT07087912 — Safety and Immunogenicity of the Live Attenuated Tetravalent Butantan-Dengue Vaccine in Autoimmune Rheumatic Diseases
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | University of Sao Paulo General Hospital |
| Enrollment | 477 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatoid Arthritis (RA); Juvenile Idiopathic Arthritis (JIA); Systemic Lupus Erythematosus (SLE); Juvenile Systemic Lupus Erythematosus; Systemic Sclerosis (SSc) |
| Interventions |
The goal of this clinical trial is to evaluate whether the live attenuated tetravalent Butantan-Dengue vaccine (Butantan-DV) is safe and capable of inducing an immune response in patients aged 12 to 59 years with autoimmune rheumatic diseases (ARDs) who are clinically stable and under low-grade or no immunosuppression, as well as in healthy volunteers matched by sex and age.
The main questions…
Active, Not Recruiting
NCT05879419 — Recombinant Herpes Zoster Vaccine in Patients With Autoimmune Rheumatic Diseases
| Status | Active, not recruiting |
| Phase | Phase 4 |
| Sponsor | University of Sao Paulo General Hospital |
| Enrollment | 2005 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatoid Arthritis; Spondylitis, Ankylosing; Spondyloarthritis; Systemic Lupus Erythematosus; Sjogren’s Syndrome |
| Interventions | ; ; |
Introduction: Patients with autoimmune rheumatic diseases (ARDs), rheumatoid arthritis (RA), juvenile idiopathic arthritis (JIA), psoriatic arthritis (PAs), ankylosing spondylitis (AS), systemic lupus erythematosus (SLE), primary Sjögren’s syndrome (pSS) , systemic sclerosis (SSc), idiopathic inflammatory myopathies (IIM) and primary vasculitides, have a high risk of herpes zoster (HZ) infectio…
NCT04483466 — Methotrexate Treatment of Arthritis Caused by Chikungunya Virus (MARCH)
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | George Washington University |
| Enrollment | 150 |
| Study Type | INTERVENTIONAL |
| Conditions | Investigate the Effect(s) of Methotrexate Treatment on Arthritis Disease Severity |
| Interventions | ; |
MARCH is the first randomized, double-blind, placebo-controlled evaluation of the efficacy and pathologic mechanism determined by synovial biopsy of 6 months of methotrexate (n=100) versus placebo (n=50) therapy for chronic chikungunya (CHIKV) arthritis in Colombia with the option for open-label use of the medication for up to one year for all participants. Our central hypothesis is that methot…
Not Yet Recruiting
NCT07034404 — Effects of a Digital Exercise Intervention on Sleep and Physical Activity in Patients With Spondyloarthritis
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | University Hospital, Grenoble |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Spondylarthritis; Spondylarthropathies; Spondylitis, Ankylosing |
| Interventions | ; |
The goal of this clinical trial is to assess whether a tailored digital Adapted Physical Activity (APA) program can improve physical activity levels and sleep quality in adults diagnosed with spondyloarthritis (SpA).
The main questions it aims to answer are:
Does participation in a 6-month digital APA program increase average daily step count (measured with an activity tracker)? Does the prog…
NCT07321418 — Mid-term Results of Epiphyseal Transfer for Hip Post Septic Epiphyseal Loss
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Assiut University |
| Enrollment | 20 |
| Study Type | OBSERVATIONAL |
| Conditions | Septic Arthritis of the Native Hip; Epiphyseal Arrest, Lower Leg |
Absence or loss of the growth plate together with the epiphysis of a long bone presents a very difficult condition to treat. An example of this is the loss of the head and neck of the femur especially as a part of severe sequelae of infantile septic arthritis.
NCT07329556 — Skin Autofluorescence Assessment of Advanced Glycation End Products in Rheumatic Diseases
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Bursa City Hospital |
| Enrollment | 300 |
| Study Type | OBSERVATIONAL |
| Conditions | Rheumatoid Arthritis (RA; Ankylosing Spondylitis; Psoriatic Arthritis; Reactive Arthritis (ReA); Crystal Arthropathies |
Rheumatic diseases are chronic inflammatory conditions that can lead to long-term tissue damage and increased cardiovascular and metabolic risk. Advanced glycation end products (AGEs) are harmful molecules that accumulate in the body over time and are known to promote inflammation and oxidative stress. Increased AGE burden has been implicated in several chronic diseases; however, its role in rh…
NCT07440238 — Evaluation of the Efficacy of Corticosteroids in Septic Arthritis in Adults
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | Assistance Publique - Hôpitaux de Paris |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Septic Arthritis |
| Interventions |
Septic arthritis is a severe infection associated with significant morbidity and mortality. Despite eradication of the microorganisms, persistent inflammation may lead to substantial long-term functional joint sequelae. The use of corticosteroids could reduce this inflammation, thereby improving functional joint outcomes and facilitating first-line medical treatment. The hypothesis of this stud…
NCT07426471 — Delafloxacin Plasma and Tissue Concentration in Patients With Skin, Soft Tissue, and Bone and Joint Infections.
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | IRCCS San Raffaele |
| Enrollment | 20 |
| Study Type | OBSERVATIONAL |
| Conditions | Soft Tissue Infections; Mediastinitis; Osteomyelitis/Septic Arthritis; Prosthetic Joint Infection |
| Interventions |
The goal of this observational study is to measure how well the antibiotic delafloxacin penetrates into the blood and various body tissues in adult patients over 18 years old. Specifically, this study focuses on patients who are receiving the drug to treat bacterial infections and are undergoing surgery for post-sternotomy wound infections, mediastinitis, or infected prosthetic joints .
The ma…
Enrolling by Invitation
NCT02422875 — Comparative Autoantibody and Immunologic Cell Marker Study
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | Emory University |
| Enrollment | 2500 |
| Study Type | OBSERVATIONAL |
| Conditions | Autoimmune Diseases; Lupus Erythematosus, Systemic; Communicable Diseases |
The purpose of this study is to compare immune phenotype, function, and specificity of B lymphocytes from different developmental stages in autoimmune patients to B cells from infectious disease patients and healthy controls.
NCT07264296 — Implant-Related Infections in Patients With Skeletal Sarcomas
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | Vastra Gotaland Region |
| Enrollment | 40 |
| Study Type | OBSERVATIONAL |
| Conditions | Implant Infection; Skeletal Sarcoma; Hip Arthritis; Prosthesis-Related Infections; Knee Arthritis |
The aim of this observational study is to gain knowledge on the microbial and immunological factors behind implant-related infections in patients with skeletal sarcoma.
The main research question the project aims to answer is:
• Are immunological factors more important than microbial factors in peri-prosthetic joint infections in orthopaedic oncology patients?
Patients with skeletal sarcoma …
Completed Trials
NCT01208792 — Auto-immunity and Pulmonary Arterial Hypertension
| Status | Completed |
| Phase | N/A |
| Sponsor | Assistance Publique - Hôpitaux de Paris |
| Enrollment | 629 |
| Study Type | INTERVENTIONAL |
| Conditions | Pulmonary Arterial Hypertension; HIV Infection; Congenital Heart Defect; Systemic Sclerosis; Connective Tissue Disease |
| Interventions | ; |
The investigators have recently evidenced the presence of antibodies to endothelial cells and fibroblasts in patients with idiopathic or SSc-associated PAH. The investigators also have identified several target antigens of anti-fibroblasts antibodies.
The objective of this study is to further investigate for the presence of antibodies to endothelial cells and fibroblasts in patients and charac…
NCT03604406 — The Immunogenicity and Safety of Zostavax® and Shingrix® in Rheumatoid Arthritis Patients Using Abatacept
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Kevin Winthrop |
| Enrollment | 154 |
| Study Type | INTERVENTIONAL |
| Conditions | Herpes Zoster; Inflammatory Disease; Rheumatoid Arthritis |
| Interventions | ; ; |
This investigator-initiated study will serve as a sub-study for the American College of Rheumatology-sponsored VERVE protocol currently funded by the NIH. This double-blinded multicenter randomized pragmatic trial is designed to determine whether Zostavax or Shingrix are safe and effective in patients with rheumatoid arthritis (RA) currently using anti-tumor necrosis factor (TNF) therapies. Inc…
NCT04075526 — Vancomycin Powder and Dilute Povidone Iodine Lavage for Infection Prophylaxis in High Risk Total Joint Arthroplasty
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | NYU Langone Health |
| Enrollment | 2129 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoarthritis |
| Interventions | ; ; |
This is a prospective, randomized, controlled, open label, parallel four-arm design, multi-center study to compare different intraoperative interventions in the prevention of acute PJI development.
NCT04530682 — COVID-19 in Rheumatic Inflammatory Diseases Under Immuno-suppressive Drugs
| Status | Completed |
| Phase | N/A |
| Sponsor | University Hospital, Montpellier |
| Enrollment | 163 |
| Study Type | OBSERVATIONAL |
| Conditions | Chronic Inflammatory Rheumatism |
| Interventions |
Accurate knowledge of the humoral immune responses induced by SARS-CoV-2 in patients undergoing immunosuppressive therapy is essential to guide recommendations for infected patients and for vaccination policy for uninfected immunosuppressed patients.
NCT05341908 — Prevalence of Pathogens in Synovial Fluid Obtained From Emergency Department Patients
| Status | Completed |
| Phase | N/A |
| Sponsor | Olive View-UCLA Education & Research Institute |
| Enrollment | 750 |
| Study Type | OBSERVATIONAL |
| Conditions | Septic Arthritis; Joint Infection |
This is a prospective, observational study of patients presenting to the emergency departments at 9 EMERGEncy ID NET sites. The objectives of the proposed study are to:
- Describe the range and proportion of infectious agents in synovial fluid as detected by standard C&S and investigational PCR testing, i.e., Biofire® Film Array® Bone and Joint Infection (BJI) Panel,
- Describe the epidemio…
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 …
NCT05570656 — Modeling Spinal Mobility in Ankylosing Spondylitis: Towards New Telekinetic Biomarkers
| Status | Completed |
| Phase | N/A |
| Sponsor | University Hospital, Montpellier |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Ankylosing Spondylitis |
| Interventions |
Ankylosing spondylitis (AS) is a chronic inflammatory rheumatic disease that mainly affects the spine and pelvis in its axial form. It is responsible for chronic inflammatory pain and sometimes ankylosis with significant functional retention.
Clinicians need markers capable of precisely measuring the restriction of range of motion in these patients, reflections of the activity and/or sequelae …
NCT05913817 — The Evaluation of Injection Site Pain and Adherence in Patients Switching From a Low To High Concentration Adalimumab (AVT-02) Across Multiple Indications.
| Status | Completed |
| Phase | N/A |
| Sponsor | Jamp Pharma Corporation |
| Enrollment | 324 |
| Study Type | OBSERVATIONAL |
| Conditions | Crohn Disease; Ulcerative Colitis; Rheumatoid Arthritis; Ankylosing Spondylitis; Psoriatic Arthritis |
| Interventions |
The purpose of the Phase IV study is to investigate the effects of both Volume and Citrate on Injection Site Pain (ISP), adherence, patient satisfaction, Quality of Life, and Disease Assessment in the Canadian Adalimumab Market.
The phase IV study is an observational, pan-Canadian, multidisciplinary study aiming to enroll 600 patients across 50-70 sites across 3 different Therapeutic Areas (GI…
NCT06698900 — This Project Aims to Understand the Needs of Rheumatologists and Other Specialties in the Care of Patients With SLE
| Status | Completed |
| Phase | N/A |
| Sponsor | AstraZeneca |
| Enrollment | 1000 |
| Study Type | OBSERVATIONAL |
| Conditions | Systemic Lupus Erythematosus |
The project will be conducted in four distinct stages. Firstly, evidence synthesis will be carried out to gather and analyze available data on the topic. Following this, a discussion among physicians will be facilitated to understand the knowledge gaps among rheumatologists and other specialists regarding SLE. Subsequently, consensus will be sought among a select group of rheumatologists on var…
NCT06489535 — Retention and Re-Engagement in Treatment for Addiction Following Serious Injection Related Infections (RETAIN)
| Status | Completed |
| Phase | N/A |
| Sponsor | Boston Medical Center |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Opioid Use Disorder; Bloodstream Infection; Osteomyelitis; Endocarditis; Septic Arthritis |
| Interventions | ; |
This project is a pilot study of an adapted intervention of an existing Opioid Use Disorder (OUD) treatment retention intervention called Recovery Management Checkups (RMC). This intervention has been adapted to better fit the experiences and unique issues of those that have been hospitalized with serious injection related infections (SIRI) based on the findings from a prior qualitative study f…
Other (Unknown)
NCT03704766 — Alpha-Defensin and Synovial Proteins to Improve Detection of Pediatric Septic Arthritis
| Status | Unknown |
| Phase | N/A |
| Sponsor | Hospital for Special Surgery, New York |
| Enrollment | 442 |
| Study Type | INTERVENTIONAL |
| Conditions | Joint Infection; Infection of Hip Joint (Disorder); Infection of Shoulder Joint; Septic Arthritis |
| Interventions | ; ; |
Differentiating between septic arthritis and other causes of joint inflammation in pediatric patients is challenging and of the utmost importance because septic arthritis requires surgical debridement as part of the treatment regimen. The current gold standard to diagnose septic arthritis in children is a positive synovial fluid culture; however, joint cultures may take several days to return. …
Other (Terminated)
NCT03827759 — Differentiate Children Septic and Inflammatory Arthritis by Comparative Analysis
| Status | Terminated |
| Phase | N/A |
| Sponsor | University Hospital, Montpellier |
| Enrollment | 100 |
| Study Type | OBSERVATIONAL |
| Conditions | Septic Arthritis; Inflammatory Arthritis; Children |
The purpose is to found new biomarker that differentiate septic arthritis and Juvenile Idiopathic Arthritis in children. Synovial liquid and blood samples with proteomic, MiRNA searching, multiplex cytokine analysis and cellular phenotyping, will be analysed. The results for each data will be compared in function of the disease to search discriminant markers. On behalf with this result specific…
Other (Suspended)
NCT04031469 — A Non-Interventional Pilot Study to Explore the Role of Gut Flora in Disease
| Status | Suspended |
| Phase | N/A |
| Sponsor | ProgenaBiome |
| Enrollment | 1000 |
| Study Type | OBSERVATIONAL |
| Conditions | Gut Microbiome; Gastrointestinal Microbiome; Autism; Autism Spectrum Disorder; Autism Spectrum Disorder High-Functioning |
| Interventions |
This study seeks to correlate microbiome sequencing data with information provided by patients and their medical records.
NCT04584541 — SarS-Cov-2 Viral Infection (COVID-19) in Patients With Chronic Inflammatory Rheumatism
| Status | Terminated |
| Phase | N/A |
| Sponsor | Assistance Publique - Hôpitaux de Paris |
| Enrollment | 150 |
| Study Type | INTERVENTIONAL |
| Conditions | Spondyloarthritis; Rheumatoid Arthritis; Covid19 |
| Interventions | ; ; |
The purpose of this study is to assess whether immunosuppressive therapies used by patients with chronic inflammatory rheumatic diseases have an impact on the viral load and the humoral and cellular responses during viral infection with SarSCoV2, compared to members of their family cluster infected with the same viral strain.
NCT04115098 — Individualizing Anti-Inflammatory Medications for Adults With Axial Spondyloarthritis: A Series of N-of 1 Trials
| Status | Terminated |
| Phase | Phase 2 |
| Sponsor | The University of Texas Health Science Center, Houston |
| Enrollment | 42 |
| Study Type | INTERVENTIONAL |
| Conditions | Axial Spondyloarthritis |
| Interventions | ; ; |
The purpose of this study is to compare selective cyclooxygenase-2 (COX-2) and non selective COX inhibitors with respect to the extent to which disease activity is improved without self reported, unacceptable side effects among individual patients with axial spondyloarthritis (AxSpA),to compare selective COX-2 and nonselective COX inhibitors impact on Health related Quality of Life (HrQOL) and …
NCT05000216 — COVID-19 Booster Vaccine in Autoimmune Disease Non-Responders
| Status | Terminated |
| Phase | Phase 2 |
| Sponsor | National Institute of Allergy and Infectious Diseases (NIAID) |
| Enrollment | 258 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatoid Arthritis (RA); Systemic Lupus Erythematosus (SLE); Pemphigus Vulgaris; Multiple Sclerosis (MS); Systemic Sclerosis (SSc) |
| Interventions | ; ; |
This is a randomized, multi-site, adaptive, open-label clinical trial comparing the immune response to different additional doses of COVID-19 vaccine in participants with autoimmune disease requiring IS medications. All study participants will have negative serologic or suboptimal responses (defined as a Roche Elecsys® Anti-SARS-CoV-2 S result ≤200 U/mL) or a low immune response (defined as a R…
NCT05156762 — Total Joint Arthroplasty (TJA) Weight Loss Study
| Status | Terminated |
| Phase | N/A |
| Sponsor | Boston Medical Center |
| Enrollment | 3 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoarthritis, Hip; Osteoarthritis, Knee; Obesity, Morbid |
| Interventions | ; ; |
This is a randomized clinical trial (RCT) to assess the efficacy of bariatric surgery vs medical weight loss vs. the “usual standard of care” to optimize a morbidly obese patient with end-stage osteoarthritis of the hip or knee joint for total joint arthroplasty (TJA).
The study population will include patients with hip or knee joint osteoarthritis and BMI (Body Mass Index) > 40 kg/m2 who are…
NCT05615701 — Image Quality of EOSedge for Radiographic Evaluation of Hip Implant
| Status | Terminated |
| Phase | N/A |
| Sponsor | University Hospital, Montpellier |
| Enrollment | 97 |
| Study Type | INTERVENTIONAL |
| Conditions | Hip Osteoarthritis; Hip Prosthesis Infection |
| Interventions |
EOSedge is a precise, low dose imaging system that delivers full body, high-quality images covering the full set of musculoskeletal and orthopedic exams.
The objective of the study is to evaluate the quality of the focused pelvis/hip X-ray images on EOSedge compared to those performed on DR (current practice) to perform a preoperative radiographic evaluation of hip implant, A sufficient image …
NCT05521880 — Anchoring Sequential Intermittent Long Acting Antimicrobials With Medication for Opioid Use Disorder (MOUD) for Invasive Infections Related to Opioid Use
| Status | Terminated |
| Phase | Phase 4 |
| Sponsor | University of Maryland, Baltimore |
| Enrollment | 2 |
| Study Type | INTERVENTIONAL |
| Conditions | Substance Use Disorders; Infection, Soft Tissue; Bacteremia; Osteomyelitis Acute; Septic Arthritis |
| Interventions |
Standard of care for patients with opioid use disorder and complicated infections is discharge to subacute nursing facilities on IV antibiotics until completion of treatment course. We aim to determine the efficacy of an alternative strategy using intermittent outpatient oritavancin therapy dosed weekly combined with initiation and continuation of medication assisted treatment for opioid use di…