Clinical Trials for Staphylococcal Infections

Currently registered clinical trials for Staphylococcal Infections from ClinicalTrials.gov. 15 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 Staphylococcal Infections from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 15
  • Active, not recruiting: 4
  • Completed: 23
  • Other: 8

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

Recruiting Trials

NCT05137119 — Staphylococcus Aureus Network Adaptive Platform Trial

StatusRecruiting
PhasePhase 4
SponsorUniversity of Melbourne
Enrollment8000
Study TypeINTERVENTIONAL
ConditionsStaphylococcus Aureus Bacteremia
Interventions; ;

The Staphylococcus aureus Network Adaptive Platform (SNAP) trial is an International Multi-Centered Randomised Adaptive Platform Clinical Trial to evaluate a range of interventions to reduce mortality for patients with Staphylococcus Aureus bacteraemia (SAB).

NCT04886284 — Combination Cefazolin With Ertapenem for Methicillin-susceptible Staphylococcus Aureus Bacteremia

StatusRecruiting
PhasePhase 2
SponsorTodd C. Lee MD MPH FIDSA
Enrollment60
Study TypeINTERVENTIONAL
ConditionsStaphylococcus Aureus Bacteremia; Staphylococcus Aureus Septicemia; Staphylococcal Sepsis; Staphylococcus Aureus Endocarditis
Interventions;

There is a variety of in vitro, in vivo (animal model), and human case series data which suggests that the addition of ertapenem to cefazolin could improve outcomes in methicillin-susceptible S. aureus bacteremia. No randomized controlled trial has been performed.

This study is an approved sub-study of The Staphylococcus aureus Network Adaptive Platform (SNAP) trial (NCT05137119)

NCT06283355 — Comparing Single Versus Repeat NMT on the Diversity of the Neonatal Nasal Microbiome

StatusRecruiting
PhasePhase 1
SponsorJohns Hopkins University
Enrollment175
Study TypeINTERVENTIONAL
ConditionsStaphylococcus Aureus; Microbial Colonization; Neonatal Infection
Interventions;

This study aims to determine whether a parent-to-child nasal microbiota transplant (NMT) can seed and engraft parental organisms into the neonatal microbiome and increase the neonatal microbiome diversity.

NCT06749457 — A Study to Evaluate AZD7760 Safety and Pharmacokinetics in Healthy Adults (Phase I) and Adults With End-stage Kidney Disease on Hemodialysis With a Central Venous Catheter (Phase IIa)

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorAstraZeneca
Enrollment231
Study TypeINTERVENTIONAL
ConditionsStaphylococcus Aureus
Interventions;

The purpose of this study is to evaluate the safety and pharmacokinetics (PK) of AZD7760 when given as an intravenous infusion to healthy participants (Phase I) or participants with end-stage kidney disease receiving hemodialysis through a central venous catheter (Phase IIa).

NCT06726395 — Comparison of Cloxacillin and Benzylpenicillin in Penicillin Susceptible S. Aureus Bacteraemia

StatusRecruiting
PhasePhase 4
SponsorRegion Skane
Enrollment420
Study TypeINTERVENTIONAL
ConditionsStaphylococcus Aureus Bacteraemia; Staphylococcal Bacteraemia; Staphylococcus Aureus Bloodstream Infections (BSI; Bacteremia); Staphylococcus (S.) Aureus Infection
Interventions;

The goal of this study is to investigate if benzylpenicillin is a better treatment option than cloxacillin in patients with penicillin-susceptible Staphylococcus aureus bacteraemia.

NCT06457386 — Echocardiography Versus no Echocardiography in S. Aureus Bacteraemia and VIRSTA Score < 3

StatusRecruiting
PhaseN/A
SponsorAssistance Publique - Hôpitaux de Paris
Enrollment700
Study TypeINTERVENTIONAL
ConditionsStaphylococcus Aureus; Bacteremia; Infective Endocarditis
Interventions;

Staphylococcus aureus is the most frequent cause of both healthcare-associated and community-acquired bloodstream infections worldwide. Infective endocarditis (IE) has been detected in 5-17% of cases and is a determinant of poor prognosis. The investigators developed a score (the VIRSTA score) based on patients’ characteristics to rule out IE with high confidence (negative predictive value (NPV…

NCT07082283 — Short-Term Atrial Pacing and Hemodynamics After Cardiac Surgery

StatusRecruiting
PhaseN/A
SponsorSaint-Joseph University
Enrollment200
Study TypeINTERVENTIONAL
ConditionsCardiac Output
Interventions;

The goal of this clinical trial is to learn whether temporary atrial pacing improves heart function after cardiac surgery under cardiopulmonary bypass (CPB). It will also help determine the best pacing rate during the first 24 hours after surgery. The main questions it aims to answer are:

  • Does atrial pacing improve cardiac output after surgery?
  • Is 70, 80, or 90 bpm the most effective pacin…

NCT06805994 — Administering NMT to Reestablish Infant Nasal Microbiome Diversity Following Intranasal Mupirocin Treatment

StatusRecruiting
PhasePhase 1
SponsorJohns Hopkins University
Enrollment175
Study TypeINTERVENTIONAL
ConditionsStaphylococcal Aureus Infection; Microbial Colonization; Pediatric Infection; S. Aureus Colonization; Microbial Transplant
Interventions;

This protocol aims to evaluate how NMT affects pediatric nasal microbiome diversity following intranasal mupirocin treatment

NCT07093749 — Perspectives on Antibiotics and Tracking Symptoms in Children

StatusRecruiting
PhaseN/A
SponsorMurdoch Childrens Research Institute
Enrollment300
Study TypeINTERVENTIONAL
ConditionsUrinary Tract Infection; Cellulitis; Impetigo; Pharyngitis; Tonsillitis
Interventions

The study will assess families’ perspectives and decision-making regarding the duration of oral antibiotic courses prescribed to children (4-17 years) who present with uncomplicated bacterial infections at the Royal Children’s Hospital (RCH) Emergency Department (ED). The study will involve (i) children discharged from ED on oral antibiotics and (ii) children transferred to Hospital-in-the-Home…

NCT06958835 — Linezolid Plus Standard of Care

StatusRecruiting
PhaseN/A
SponsorUniversity Hospital, Basel, Switzerland
Enrollment606
Study TypeINTERVENTIONAL
ConditionsStaphylococcus Aureus Bloodstream Infections (BSI; Bacteremia)
Interventions;

The aim of the study is to assess whether targeting virulence factors by administering linezolid in addition to standard antibiotic treatment improves outcomes in patients with Staphylococcus aureus bacteraemia.

NCT07313215 — Rifampin-combined Antibiotic Therapy for Staphylococcal PJI

StatusRecruiting
PhaseN/A
SponsorFirst Affiliated Hospital of Fujian Medical University
Enrollment428
Study TypeINTERVENTIONAL
ConditionsPeriprosthetic Joint Infection
Interventions

This is a prospective, multicenter, randomized controlled study. Patients were evaluated through inclusion and exclusion criteria. Patients who meet the conditions will sign an informed consent form. After DAIR surgery, they will be treated with intravenous antibiotics for 1-2 weeks and then randomly assigned to one of the following two groups: Antibiotic treatment group: All enrolled patients …

NCT07428265 — Comparison of Wound Healing for Diabetic Carbuncle Treated With Incision and Drainage Technique Using Cruciate Incision vs Saucerization Technique Both Followed by Vacuum Assisted Closure.

StatusRecruiting
PhaseN/A
SponsorKing Edward Medical University
Enrollment124
Study TypeINTERVENTIONAL
ConditionsCarbuncle
Interventions;

The goal of this clinical trial is to compare the effectiveness of two surgical techniques for wound healing in diabetic patients aged 25-70 years with a carbuncle requiring surgical drainage. The main questions it aims to answer are:

Is there a difference in blood loss during surgery between the two techniques?

Is there a difference in the duration required for wound healing between the two …

NCT06848387 — Unbound Cloxacillin Concentrations During Continuous Infusion

StatusRecruiting
PhasePhase 4
SponsorEmeli Månsson
Enrollment25
Study TypeINTERVENTIONAL
ConditionsStaphylococcal Infections
Interventions

Cloxacillin is the first-line choice for the treatment of severe infections caused by the bacterium Staphylococcus aureus in Sweden. Over the past year, cloxacillin is increasingly administred through continuous infusion. In this study, the free (unbound) concentration of cloxacillin when administered as a continuous infusion will be measured to ensure that the free concentration is neither too…

NCT07345325 — Rifampin-free Regimen Versus Rifampin-containing Regimen in the Treatment of Staphylococcal Prosthetic Valve Endocarditis

StatusRecruiting
PhasePhase 3
SponsorNantes University Hospital
Enrollment422
Study TypeINTERVENTIONAL
ConditionsInfective Endocarditis
Interventions;

The primary objective of this study is to demonstrate that a rifampin-free regimen is non-inferior to the rifampin-containing regimen in terms of all-cause mortality in staphylococcal prosthetic valve endocarditis within 6 months after randomization.

NCT06479837 — Modeling Host-Pathogen Interaction Using Lymphoid Organoids

StatusRecruiting
PhaseN/A
SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Enrollment500
Study TypeOBSERVATIONAL
ConditionsStaphylococcal Infections

Background:

Staphylococcus aureus (S.aureus) are bacteria that can make people sick. Sometimes, an S. aureus infection can develop inside the spine; these infections can lead to paralysis and death. Researchers do not know how S. aureus interacts with a person s cells to cause infections in the spine.

Objective:

To learn how S. aureus interacts with cells in the body using tissues from tonsi…

Active, Not Recruiting

NCT01879761 — Immune Resolution After Staphylococcus Aureus Bacteremia

StatusActive, not recruiting
PhaseN/A
SponsorUniversity of Chicago
Enrollment102
Study TypeOBSERVATIONAL
ConditionsImmune Response To Sepsis; Staphylococcus Aureus Infection

The purpose of this study is to determine how monocyte HLA-DR and other markers of immune function change with time in patients with and without prior immune dysfunction who survive sepsis from Staphylococcus aureus bacteremia.

We hypothesize that patients with prior immune dysfunction will have greater reductions in HLA-DR and other markers of immune function after an episode of sepsis than p…

NCT05695196 — Feasibility and Safety Study of Parent-to-Child Nasal Microbiota Transplant

StatusActive, not recruiting
PhasePhase 1
SponsorJohns Hopkins University
Enrollment34
Study TypeINTERVENTIONAL
ConditionsStaphylococcus Aureus; Microbial Colonization; Neonatal Infection
Interventions;

This feasibility and safety pilot study looks to determine whether transferring a parents healthy, diverse nasal microbiota to the participant’s infant(s) will create a healthy, diverse neonatal nasal microbiome.

NCT06368856 — Pharmacology of Mupirocin in Nasal Application in Healthy Volunteers: Monocentric Study

StatusActive, not recruiting
PhasePhase 1
SponsorCentre Hospitalier Universitaire de Saint Etienne
Enrollment40
Study TypeINTERVENTIONAL
ConditionsHealthy; Staphylococcus Aureus Infection
Interventions; ;

Mupirocin is an old antibiotic used topically since the 1970s. Initially used in the treatment of skin infections for its antistaphylococcal action, it is now part of the decolonization strategy for Staphylococcus aureus (SA) carriage, in association with chlorhexidine. This decolonization strategy has been recommended in France for preoperative cardiac surgery in nasal SA carriers since 2013 b…

NCT07155590 — Subphenotype- and Complication-guided Adjunctive Fosfomycin Therapy for Staphylococcus Aureus Bacteraemia

StatusActive, not recruiting
PhaseN/A
SponsorHospital Universitari de Bellvitge
Enrollment369
Study TypeOBSERVATIONAL
ConditionsStaphylococcal Aureus Infection; Staphylococcus Aureus Bacteraemia

Staphylococcus aureus bacteraemia (SAB) is a major global cause of sepsis-related mortality. Randomised trials of adjunctive antibiotics, including fosfomycin, have not shown consistent benefit, possibly due to inclusion of unselected SAB populations. The FEN-AUREUS classification enables early risk stratification based on clinical subphenotypes. The investigators aim to validate this framework…

Not Yet Recruiting

NCT07280598 — Safety of Combined Intravenous Antibiotic and Bacteriophage Therapy in Adults With Cystic Fibrosis and Antibiotic-Resistant Lung Infections

StatusNot yet recruiting
PhasePhase 1
SponsorUniversity of California, San Diego
Enrollment30
Study TypeINTERVENTIONAL
ConditionsCF - Cystic Fibrosis; Klebsiella Pneumoniae Infection; E Coli Infections; Staphylococcus Aureus Infection; Achromobacter
Interventions

This is a Phase 1, open-label, multi-center pilot study evaluating the safety and microbiological activity of intravenous (IV) bacteriophage therapy in combination with standard IV antibiotics in adults with cystic fibrosis (CF) experiencing pulmonary exacerbations due to antibiotic-resistant bacterial infections. Eligible participants will receive a 7-day course of IV antibiotics, selected by …

NCT07333378 — Retention of Vernix Caseosa in Newborns for Primary Prevention of Atopic Dermatitis

StatusNot yet recruiting
PhaseN/A
SponsorPontificia Universidad Catolica de Chile
Enrollment1383
Study TypeINTERVENTIONAL
ConditionsAtopic Dermatitis
Interventions;

Atopic dermatitis (AD), also known as eczema, is a common chronic inflammatory skin disease that usually begins in infancy and causes significant itching, discomfort, and sleep disturbance. It affects up to one in five children worldwide and represents a growing public-health problem. Research has shown that genetic and environmental factors contribute to its development, especially those relat…

NCT07384702 — Adjuvant Clopidogrel in Staphylococcus Aureus Bacteremia

StatusNot yet recruiting
PhasePhase 2
SponsorFundación Pública Andaluza para la gestión de la Investigación en Sevilla
Enrollment230
Study TypeINTERVENTIONAL
ConditionsBacteremia Due to Staphylococcus Aureus
Interventions;

The CLOPI-SNAP study is a randomized, multicenter, open-label clinical trial embedded within the SNAP (NCT 05137119) research platform. It constitutes a sub-study added to the core protocol for patients suffering Staphylococcus aureus bacteremia (SAB).

NCT07524894 — Staph Nasal Decolonization to Improve Function and Feeding

StatusNot yet recruiting
PhasePhase 2
SponsorDavid Palma
Enrollment126
Study TypeINTERVENTIONAL
ConditionsRadiation Mucositis; Staphylococcal Aureus Infection; Head and Neck Cancer
Interventions;

Radiation therapy is a type of treatment that involves using radiation beams targeted at a cancer to destroy the cancer cells or slow their growth. This type of treatment has helped many cancer patients for decades and is intended to kill cancer cells directly. Patients with head and neck cancer are commonly treated with radiation, sometimes after surgery and sometimes the radiation is delivere…

NCT07635433 — Thermosensitive Gel Nasal Spray With Stem Cell Exosomes, Mupirocin, and DNase I for Chronic Sinusitis

StatusNot yet recruiting
PhaseEarly Phase 1
SponsorThe First Affiliated Hospital of Xinxiang Medical College
Enrollment108
Study TypeINTERVENTIONAL
ConditionsChronic Rhinosinusitis With Nasal Polyps
Interventions; ;

This study tests a new nasal spray for adults (18-65 years) with chronic rhinosinusitis (CRS) without nasal polyps. The spray contains a temperature-sensitive gel (thermosensitive gel) that turns into a soft gel inside the nose to slowly release three active ingredients: human umbilical cord mesenchymal stem cell exosomes (hUC-MSC-Exo) to help heal the nasal lining, mupirocin (an antibiotic tha…

NCT02664740 — Standard Treatment Associated With Phage Therapy Versus Placebo for Diabetic Foot Ulcers Infected by S. Aureus

StatusNot yet recruiting
PhasePhase 1 / Phase 2
SponsorCentre Hospitalier Universitaire de Nīmes
Enrollment60
Study TypeINTERVENTIONAL
ConditionsDiabetic Foot; Staphylococcal Infections
Interventions;

The primary objective of this study is to compare the efficacy of standard treatment associated with a topical anti-staphylococcal bacteriophage cocktail versus standard treatment plus placebo for diabetic foot ulcers monoinfected by methicillin-resistant or susceptible S. aureus (MRSA or MSSA) as measured by the relative reduction in wound surface area (%) at 12 weeks.

Completed Trials

NCT00475930 — Chlorhexidine Impregnated Cloths to Prevent Skin and Soft Tissue Infections in Marine Officer Candidates

StatusCompleted
PhaseN/A
SponsorHenry M. Jackson Foundation for the Advancement of Military Medicine
Enrollment1563
Study TypeINTERVENTIONAL
ConditionsStaphylococcus Aureus; Community-acquired Infections; Staphylococcal Skin Infections
Interventions;

Outbreaks of skin and soft tissue infections (SSTI) related to community associated Methicillin-resistant Staphylococcus aureus (MRSA) have become increasingly common in military training units. Risk factors for MRSA related SSTI such as crowding, poor hygiene and shared equipment are often hard to avoid in a military training environment, often designed to simulate battlefield conditions.

It …

StatusCompleted
PhaseN/A
SponsorCentre Hospitalier Universitaire de Nīmes
Enrollment278
Study TypeOBSERVATIONAL
ConditionsDiabetic Foot; Staphylococcus Aureus
Interventions

The presence of S aureus in the nasal passages of diabetic patients may be a risk factor for diabetic foot lesion infections. Our aim is to compare the genetic profiles of S aureus strains found in the noses and on the foot lesions of diabetic patients. The investigators are also studying the virulence of these strains, the prevalance of S aureus at either site, and whether or not the quantity …

NCT07285759 — Investigation of Antibacterial Effect of Levobupivacaine on Staphylococcus Aureus

StatusCompleted
PhaseN/A
SponsorDokuz Eylul University
Enrollment40
Study TypeINTERVENTIONAL
ConditionsStaphylococcus Aureus Bacterial Contamination
Interventions; ;

This experimental in vitro study aimed to investigate the antibacterial effect of levobupivacaine on Staphylococcus aureus in a patient-controlled analgesia (PCA) model at concentrations commonly used for postoperative pain treatment (0.125%) and painless labour (0.0625%). The antibacterial activity was evaluated using colony count reduction and supported by Scanning Electron Microscope (SEM) i…

NCT02798497 — Panton Valentine Leucocidin

StatusCompleted
PhaseN/A
SponsorHospices Civils de Lyon
Enrollment234
Study TypeINTERVENTIONAL
ConditionsStaphylococcus Aureus Pneumonias
Interventions

Staphylococcus aureus expresses a variety of virulence factors, including Panton Valentine leukocidin (PVL), a cytotoxin. PVL is specifically associated with primary skin and soft-tissue infections and severe necrotizing pneumonia (Gillet et al. Lancet, 2002;359:753-9). PVL-positive S. aureus pneumonia is often preceded by influenza-like symptoms, and is mainly characterized by hemoptysis, pleu…

NCT02812446 — Staphylokinase and ABO Group Phenotype: New Players in Staphylococcus Aureus Implant-associated Infections Development

StatusCompleted
PhaseN/A
SponsorNantes University Hospital
Enrollment88
Study TypeOBSERVATIONAL
ConditionsStaphylococcal Infection
Interventions;

The purpose of this study is to identify bacterial and/or clinical features involved in the pathogenesis of Staphylococcus aureus implant-associated infections (IAI). Materials & methods: In total, 57 IAI S. aureus and 31 nasal carriage (NC) S. aureus isolates were studied. Staphylococcus aureus genetic background was obtained by microarray analysis. Multilocus sequence typing was performed to…

NCT02219165 — Efficacy of IntraVenous ImmunoGlobulins in Toxic Shock Syndromes: a Paediatric Pilot Study

StatusCompleted
PhasePhase 2
SponsorHospices Civils de Lyon
Enrollment30
Study TypeINTERVENTIONAL
ConditionsToxic Shock Syndrome
Interventions;

Staphylococcus aureus and Streptococcus pyogenes produce many virulence factors. Some of them are responsible for severe infections in humans. Superantigen toxins synthesized by S. aureus or by S. pyogenes, are responsible for toxic shock syndromes (TSS) which lethality can attain 25% in children with validated criteria of septic shock.

Previous studies, performed in vitro and in vivo in anima…

NCT02357966 — Safety & Efficacy of True Human Antibody, 514G3, in Staphylococcus Aureus Bacteremia Hospitalized Subjects.

StatusCompleted
PhasePhase 1 / Phase 2
SponsorXBiotech, Inc.
Enrollment52
Study TypeINTERVENTIONAL
ConditionsStaphylococcus Aureus Bacteremia
Interventions; ;

This study is a Phase I/II, double-blind, placebo-controlled trial investigating the True Human monoclonal antibody 514G3 in subjects hospitalized with Staphylococcus aureus bacteremia. Phase I involves dose escalation to evaluate potential toxicity and establish the recommended phase 2 dosage of 514G3. In Phase II (dose expansion), eligible subjects will be randomized at a ratio of 2:1 to rece…

NCT02572791 — Staph Household Intervention for Eradication (SHINE)

StatusCompleted
PhasePhase 4
SponsorWashington University School of Medicine
Enrollment835
Study TypeINTERVENTIONAL
ConditionsSkin and Subcutaneous Tissue Bacterial Infections; Staphylococcus Aureus; MRSA - Methicillin Resistant Staphylococcus Aureus Infection
Interventions; ;

The investigators propose a pragmatic comparative effectiveness trial evaluating several decolonization strategies in patients with Staphylococcus aureus infection, their household contacts, and household environmental surfaces. The central hypothesis of this proposal is that an integrated approach of periodic personal and household environmental hygiene will reduce S. aureus transmission in ho…

NCT02378493 — Evaluation of the Antibiofilmogramme® Test During Diabetic Foot Infections

StatusCompleted
PhaseN/A
SponsorCentre Hospitalier Universitaire de Nīmes
Enrollment33
Study TypeINTERVENTIONAL
ConditionsDiabetic Foot; Staphylococcus Aureus
Interventions

This is an observational study that does not change routine care.

The primary objective of this study is to investigate the role of antibiogramme-antibiofilmogramme concordance (in terms of S. aureus strains and prescribed antibiotics) in the presence/absence of S. aureus strains at the end of a first regimen of antibiotics.

NCT02694458 — Comparison of Two Dosage Adjustment Strategies of Vancomycin in Children

StatusCompleted
PhaseN/A
SponsorAssistance Publique - Hôpitaux de Paris
Enrollment100
Study TypeINTERVENTIONAL
ConditionsMethicillin-resistant Staphylococcal Infections
Interventions;

Vancomycin is the standard first-line treatment for MRSA infections and a first-line empiric therapy. The relationship between exposure to vancomycin and efficacy is admitted but because of an important intersubject variability, therapeutic exposure isn’t usually achieved.

The primary aim of this randomized controlled trial is to evaluate a new early dosage adjustment strategy of vancomycin in…

NCT03489629 — STaph Aureus Resistance-Treat Early and Repeat (STAR-TER)

StatusCompleted
PhasePhase 2
SponsorUniversity of North Carolina, Chapel Hill
Enrollment37
Study TypeINTERVENTIONAL
ConditionsCystic Fibrosis
Interventions; ;

To evaluate the micro-biologic efficacy and safety of a streamlined treatment for early onset methicillin-resistant staphylococcus aureus (MRSA) in patients with cystic fibrosis.

NCT03248063 — Non-inferiority Trial Comparing Cloxacillin vs Cefazolin in Methicillin-susceptible Staphylococcus Aureus Bacteremia

StatusCompleted
PhaseN/A
SponsorAssistance Publique - Hôpitaux de Paris
Enrollment315
Study TypeINTERVENTIONAL
ConditionsBacteremia Due to Methicillin Susceptible Staphylococcus Aureus
Interventions;

“Methicillin-susceptible Staphylococcus aureus (MSSA) bacteremia remains a major cause of community- or hospital-acquired bloodstream infections with an overall mortality estimated around 25%. Anti-staphylococcal penicillins (APs) such as oxacillin or cloxacillin are recommended as first-line agents. With the exception of first-generation cephalosporin (1GC) such as cefazolin, no alternative ha…

NCT04657185 — Reducing Perioperative S. Aureus Transmission Via OR PathTrac

StatusCompleted
PhaseN/A
SponsorGeorgetown University
Enrollment804
Study TypeOBSERVATIONAL
ConditionsS. Aureus Transmission; Surgical Site Infection
Interventions

Healthcare-associated infections (HAIs) occur frequently and are associated with patient harm. It is important that healthcare facilities take the necessary steps to prevent the spread of resistant bacteria. ESKAPE bacteria (Enterococcus, S. aureus, Klebsiella, Acinetobacter, Pseudomonas, and Enterobacter spp.) are particularly pathogenic. Isolation of these pathogens from intraoperative reserv…

NCT04274348 — Staphylococcal Toxins in Atopic Dermatitis and Eczema Herpeticum

StatusCompleted
PhaseN/A
SponsorPoitiers University Hospital
Enrollment41
Study TypeINTERVENTIONAL
ConditionsAtopic Dermatitis; Staphylococcus Aureus; Bacterial Toxins; Immune Response; Cytokines
Interventions

Atopic dermatitis (AD) is the most common chronic inflammatory skin disease. Clinical studies have demonstrated a link between staphylococcal skin colonization and the pathogenesis of AD, but the implication of bacterial virulence factors remains largely uncharacterized. Finally, AD is often associated with herpes simplex skin infections. The aim of this project is to investigate the role of st…

NCT05184764 — Study Evaluating Safety, Tolerability, and Efficacy of Intravenous AP-SA02 in Subjects With S. Aureus Bacteremia

StatusCompleted
PhasePhase 1 / Phase 2
SponsorArmata Pharmaceuticals, Inc.
Enrollment56
Study TypeINTERVENTIONAL
ConditionsBacteremia; Staphylococcus Aureus; Staphylococcus Aureus Bacteremia; Bacteremia Staph; Bacteremia Due to Staphylococcus Aureus
Interventions;

Phase 1b/2a, Randomized, Double-Blind, Placebo-Controlled, Multiple Ascending Dose Escalation Study of the Safety, Tolerability, and Efficacy of Intravenous AP SA02 as an Adjunct to Best Available Antibiotic Therapy Compared to Best Available Antibiotic Therapy Alone for the Treatment of Adults With Bacteremia Due to Staphylococcus aureus

NCT06249451 — Staphylococcus Aureus Bacteraemia (SAB)-Support-Study

StatusCompleted
PhaseN/A
SponsorUniversity Medicine Greifswald
Enrollment124
Study TypeINTERVENTIONAL
ConditionsStaphylococcus Aureus Bacteremia
Interventions

The main objective of this study is to investigate whether checklist-based close telephone consultation and process surveillance for S. aureus bacteraemia (SAB) can improve adherence to our in-house SAB-guidelines (prospective quality- improvement group).

In addition, the effects of telephone consultation on the clinical outcome of patients will be examined.

NCT06210594 — Staph Intervention for Effective Local Defense

StatusCompleted
PhasePhase 4
SponsorJohns Hopkins Bloomberg School of Public Health
Enrollment78
Study TypeINTERVENTIONAL
ConditionsStaphylococcus Aureus Infection
Interventions;

Indigenous persons experience a high burden of Staphylococcus aureus (SA) invasive disease and skin and soft tissue infections. SA carriage on the skin is factor for development of SA infections. The goal of this clinical trial is to evaluate a community-informed approach to reduce carriage of SA. Participants will be assigned to education and household supplies for prevention of SA with and wi…

NCT06338176 — Optimizing the Management of Staphylococcus Aureus Bacteremia (OPTIMUS-SAB)

StatusCompleted
PhaseN/A
SponsorUniversity of Alberta
Enrollment2542
Study TypeINTERVENTIONAL
ConditionsStaph Aureus Bacteremia
Interventions

Staphylococcus aureus bacteremia (SAB) is associated with high morbidity and mortality rates with an incidence disproportionately higher in vulnerable populations. Management according to evidence-based care parameters, in particular Infectious Diseases (ID) consultation, is associated with improved mortality. SAB management is suboptimal in Alberta compared to other jurisdictions. An Alberta-b…

NCT07428915 — Evaluating Legit.Health Plus Support for Improving Diagnosis of Generalized Pustular Psoriasis and Other Skin Conditions Among Primary Care Physicians and Dermatologists

StatusCompleted
PhaseN/A
SponsorAI Labs Group S.L
Enrollment15
Study TypeOBSERVATIONAL
ConditionsPustular Psoriasis (PP); Generalized Pustular Psoriasis (GPP); Eczema Atopic Dermatitis; Acute Generalized Exanthematous Pustulosis; Acne
Interventions

This study aims to determine if an artificial intelligence (AI) medical device can help healthcare professionals more accurately diagnose rare and complex skin conditions. Dermatological issues are common in primary care, but there is often a gap in diagnostic accuracy between general practitioners and specialists, which can lead to treatment delays for serious conditions like Generalized Pustu…

NCT06702878 — Light-Activated Antimicrobial Therapy to Prevent Surgical Site Infections

StatusCompleted
PhasePhase 3
SponsorOndine Biomedical Inc.
Enrollment4787
Study TypeINTERVENTIONAL
ConditionsSurgical Site Infections; Surgical Wound Infection; Infections; Anti-Infective Agents
Interventions

This is a Phase 3 multi-center, group-randomized, crossover trial to compare nasal antimicrobial photodisinfection therapy (aPDT) with standard of care for prevention of surgical site infections in patients undergoing major elective, urgent, or emergent surgeries in a hospital setting. The main outcomes are to:

  1. compare the efficacy, and
  2. estimate the safety of applying nasal (aPDT) before…

NCT07322549 — Amoxicillin/Clavulanic Acid Susceptibility in Acute Community-acquired Pneumonia Requiring Intensive Care Management

StatusCompleted
PhaseN/A
SponsorCentre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Enrollment104
Study TypeOBSERVATIONAL
ConditionsSevere Community-acquired Pneumonia
Interventions;

Severe community-acquired pneumonia (CAP) and community-acquired aspiration pneumonia (CAAP) are common reasons for adult emergency department visits and subsequent admission to the intensive care unit (ICU). Three bacteria are primarily implicated in this type of pneumonia: Streptococcus pneumoniae, Haemophilus influenzae, and Staphylococcus aureus.

Empirical antibiotic therapy for this condi…

NCT06633588 — Decolonization Efficacy of Polyhexanide vs. Mupirocin

StatusCompleted
PhasePhase 4
SponsorSwiss Paraplegic Research, Nottwil
Enrollment24
Study TypeINTERVENTIONAL
ConditionsStaphylococcus Aureus; Colonization, Asymptomatic
Interventions;

This pilot randomized controlled trial evaluates the feasibility, tolerability, and preliminary efficacy of a decolonization regimen using polyhexanide in reducing Staphylococcus aureus colonization in the preoperative phase of elective spine surgery, compared to the standard mupirocin and chlorhexidine regimen. The trial involves 24 participants randomized into two groups: one receiving polyhe…

NCT07189858 — Light-Activated Antimicrobial Therapy to Prevent Surgical Site Infections - Canada

StatusCompleted
PhaseN/A
SponsorOndine Biomedical Inc.
Enrollment401
Study TypeINTERVENTIONAL
ConditionsSurgical Site Infections; Infections; Surgical Wound Infections; Anti-Infective Agents
Interventions

This is a Phase 4 multi-center, group-randomized, crossover trial to compare nasal antimicrobial photodisinfection therapy (aPDT) with standard of care for prevention of surgical site infections in patients undergoing major elective, urgent, or emergent surgeries in a hospital setting. The main outcomes are to:

  1. compare the efficacy, and
  2. estimate the safety of applying nasal (aPDT) before…

Other (Terminated)

NCT03869593 — Role of the NLRP3 Inflammasome in Escherichia Coli and Staphylococcus Aureus Bacteria

StatusTerminated
PhaseN/A
SponsorCentre Hospitalier Universitaire de Nice
Enrollment60
Study TypeOBSERVATIONAL
ConditionsEscherichia Coli Infections; Staphylococcus Aureus
Interventions

Our previous studies delineate a novel pathway of immune activation in animals that the investigators have named Anti-Virulence Immunity (AVI). Using a mice model of bacteremia, the investigators have demonstrated that Escherichia coli Cytotoxic Necrotizing Factor 1 (CNF1) activity is sensed by the immune system. This immune sensing results in a rapid bacterial clearing during bacteremia trigge…

NCT05710393 — Hidradenitis - an Analysis of Genetic Traits and Linkages in Families

StatusTerminated
PhaseN/A
SponsorUniversity of Chicago
Enrollment97
Study TypeOBSERVATIONAL
ConditionsHidradenitis Suppurativa

The aim of this study is to find a genetic link or family trait connecting persons with Hidradenitis Suppurativa (HS) to each other. As a result, discover the cause and perhaps treatment for Hidradenitis Suppurativa (HS).