Clinical Trials for Infectious Arthritis

Currently registered clinical trials for Infectious Arthritis from ClinicalTrials.gov. 22 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 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

StatusRecruiting
PhaseN/A
SponsorYale University
Enrollment5000
Study TypeOBSERVATIONAL
ConditionsRheumatic 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

StatusRecruiting
PhasePhase 4
SponsorMurdoch Childrens Research Institute
Enrollment285
Study TypeINTERVENTIONAL
ConditionsBone 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

StatusRecruiting
PhaseN/A
SponsorZimmer Biomet
Enrollment380
Study TypeOBSERVATIONAL
ConditionsArthroplasty 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

StatusRecruiting
PhaseN/A
SponsorXiaojuan Li
Enrollment88
Study TypeOBSERVATIONAL
ConditionsBone 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.

StatusRecruiting
PhasePhase 2 / Phase 3
SponsorUniversity Hospital, Linkoeping
Enrollment1100
Study TypeINTERVENTIONAL
ConditionsArthroplasty, 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

StatusRecruiting
PhaseN/A
SponsorM.D. Anderson Cancer Center
Enrollment125
Study TypeOBSERVATIONAL
ConditionsAnkylosing 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

StatusRecruiting
PhaseN/A
SponsorOttawa Hospital Research Institute
Enrollment7600
Study TypeINTERVENTIONAL
ConditionsHip 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

StatusRecruiting
PhaseN/A
SponsorBrain Inflammation Collaborative
Enrollment10000
Study TypeOBSERVATIONAL
ConditionsPost-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

StatusRecruiting
PhaseN/A
SponsorOregon Health and Science University
Enrollment125
Study TypeOBSERVATIONAL
ConditionsAnterior 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

StatusRecruiting
PhaseN/A
SponsorIstanbul Physical Medicine Rehabilitation Training and Research Hospital
Enrollment76
Study TypeOBSERVATIONAL
ConditionsAnkylosing 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

StatusRecruiting
PhaseN/A
SponsorSheffield Children’s NHS Foundation Trust
Enrollment30
Study TypeOBSERVATIONAL
ConditionsMusculoskeletal 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

StatusRecruiting
PhasePhase 1
SponsorShanghai Qilu Pharmaceutical Research and Development Center LTD
Enrollment102
Study TypeINTERVENTIONAL
ConditionsAtopic 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

StatusRecruiting
PhaseN/A
SponsorSemmelweis University
Enrollment300
Study TypeOBSERVATIONAL
ConditionsKidney 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

StatusRecruiting
PhasePhase 4
SponsorIndiana University
Enrollment100
Study TypeINTERVENTIONAL
ConditionsMethicillin 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

StatusRecruiting
PhaseN/A
SponsorCharite University, Berlin, Germany
Enrollment130
Study TypeINTERVENTIONAL
ConditionsHip 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

StatusRecruiting
PhaseN/A
SponsorSonoma Biotherapeutics, Inc.
Enrollment36
Study TypeOBSERVATIONAL
ConditionsRheumatoid 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

StatusRecruiting
PhasePhase 2
SponsorAkiva Mintz
Enrollment200
Study TypeINTERVENTIONAL
ConditionsHealthy 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

StatusRecruiting
PhaseN/A
SponsorBahattin Kemah
Enrollment90
Study TypeINTERVENTIONAL
ConditionsOsteoarthritis, 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)

StatusRecruiting
PhasePhase 1
SponsorUCB Biopharma SRL
Enrollment20
Study TypeINTERVENTIONAL
ConditionsModerate 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

StatusRecruiting
PhaseN/A
SponsorDiakonhjemmet Hospital
Enrollment350
Study TypeOBSERVATIONAL
ConditionsArthritis; 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

StatusRecruiting
PhaseN/A
SponsorNovartis Pharmaceuticals
Enrollment76
Study TypeOBSERVATIONAL
ConditionsHidradenitis 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

StatusRecruiting
PhasePhase 4
SponsorUniversity of Sao Paulo General Hospital
Enrollment477
Study TypeINTERVENTIONAL
ConditionsRheumatoid 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

StatusActive, not recruiting
PhasePhase 4
SponsorUniversity of Sao Paulo General Hospital
Enrollment2005
Study TypeINTERVENTIONAL
ConditionsRheumatoid 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)

StatusActive, not recruiting
PhasePhase 3
SponsorGeorge Washington University
Enrollment150
Study TypeINTERVENTIONAL
ConditionsInvestigate 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

StatusNot yet recruiting
PhaseN/A
SponsorUniversity Hospital, Grenoble
Enrollment100
Study TypeINTERVENTIONAL
ConditionsSpondylarthritis; 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

StatusNot yet recruiting
PhaseN/A
SponsorAssiut University
Enrollment20
Study TypeOBSERVATIONAL
ConditionsSeptic 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

StatusNot yet recruiting
PhaseN/A
SponsorBursa City Hospital
Enrollment300
Study TypeOBSERVATIONAL
ConditionsRheumatoid 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

StatusNot yet recruiting
PhasePhase 2
SponsorAssistance Publique - Hôpitaux de Paris
Enrollment200
Study TypeINTERVENTIONAL
ConditionsSeptic 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.

StatusNot yet recruiting
PhaseN/A
SponsorIRCCS San Raffaele
Enrollment20
Study TypeOBSERVATIONAL
ConditionsSoft 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

StatusEnrolling by invitation
PhaseN/A
SponsorEmory University
Enrollment2500
Study TypeOBSERVATIONAL
ConditionsAutoimmune 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.

StatusEnrolling by invitation
PhaseN/A
SponsorVastra Gotaland Region
Enrollment40
Study TypeOBSERVATIONAL
ConditionsImplant 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

StatusCompleted
PhaseN/A
SponsorAssistance Publique - Hôpitaux de Paris
Enrollment629
Study TypeINTERVENTIONAL
ConditionsPulmonary 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

StatusCompleted
PhasePhase 2
SponsorKevin Winthrop
Enrollment154
Study TypeINTERVENTIONAL
ConditionsHerpes 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

StatusCompleted
PhasePhase 1
SponsorNYU Langone Health
Enrollment2129
Study TypeINTERVENTIONAL
ConditionsOsteoarthritis
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

StatusCompleted
PhaseN/A
SponsorUniversity Hospital, Montpellier
Enrollment163
Study TypeOBSERVATIONAL
ConditionsChronic 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

StatusCompleted
PhaseN/A
SponsorOlive View-UCLA Education & Research Institute
Enrollment750
Study TypeOBSERVATIONAL
ConditionsSeptic 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:

  1. 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,
  2. Describe the epidemio…

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 …

NCT05570656 — Modeling Spinal Mobility in Ankylosing Spondylitis: Towards New Telekinetic Biomarkers

StatusCompleted
PhaseN/A
SponsorUniversity Hospital, Montpellier
Enrollment40
Study TypeINTERVENTIONAL
ConditionsAnkylosing 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.

StatusCompleted
PhaseN/A
SponsorJamp Pharma Corporation
Enrollment324
Study TypeOBSERVATIONAL
ConditionsCrohn 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

StatusCompleted
PhaseN/A
SponsorAstraZeneca
Enrollment1000
Study TypeOBSERVATIONAL
ConditionsSystemic 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…

StatusCompleted
PhaseN/A
SponsorBoston Medical Center
Enrollment40
Study TypeINTERVENTIONAL
ConditionsOpioid 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

StatusUnknown
PhaseN/A
SponsorHospital for Special Surgery, New York
Enrollment442
Study TypeINTERVENTIONAL
ConditionsJoint 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

StatusTerminated
PhaseN/A
SponsorUniversity Hospital, Montpellier
Enrollment100
Study TypeOBSERVATIONAL
ConditionsSeptic 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

StatusSuspended
PhaseN/A
SponsorProgenaBiome
Enrollment1000
Study TypeOBSERVATIONAL
ConditionsGut 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

StatusTerminated
PhaseN/A
SponsorAssistance Publique - Hôpitaux de Paris
Enrollment150
Study TypeINTERVENTIONAL
ConditionsSpondyloarthritis; 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

StatusTerminated
PhasePhase 2
SponsorThe University of Texas Health Science Center, Houston
Enrollment42
Study TypeINTERVENTIONAL
ConditionsAxial 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

StatusTerminated
PhasePhase 2
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment258
Study TypeINTERVENTIONAL
ConditionsRheumatoid 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

StatusTerminated
PhaseN/A
SponsorBoston Medical Center
Enrollment3
Study TypeINTERVENTIONAL
ConditionsOsteoarthritis, 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

StatusTerminated
PhaseN/A
SponsorUniversity Hospital, Montpellier
Enrollment97
Study TypeINTERVENTIONAL
ConditionsHip 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 …

StatusTerminated
PhasePhase 4
SponsorUniversity of Maryland, Baltimore
Enrollment2
Study TypeINTERVENTIONAL
ConditionsSubstance 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…