[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"enterococcus-faecalis-infection\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:enterococcus-faecalis-infection":25},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,46,76],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":28,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100580153","antimicrobial-combination-therapy-for-treatment-of-enterococcus-faecalis-bacteremia-100580153",false,"NCT06833593","Antimicrobial Combination Therapy for Treatment of Enterococcus Faecalis Bacteremia","Efficacy of Optimized Antimicrobial Combination Therapy for Treatment of Enterococcus Faecalis Bacteremia and Identification of Intestinal Microbiota Signature","MicroEFfAECT","Inclusion Criteria:\n\n* Adult (≥18 years)\n* Monomicrobial EF-BSI\n* Receipt of ≥ 5 days of at least one in vitro active drug (ampicillin, amoxicillin\u002Fclavulanate, ampicillin\u002Fsulbactam, piperacillin, vancomycin, teicoplanin, daptomycin and linezolid) with or without a synergistic drug (ceftriaxone, gentamycin, streptomycin), at common suggested dosages for EF-BSI in empirical or definitive therapy\n* Written informed consent\n\nExclusion Criteria:\n\n* Short term (within 3 days from BSI) mortality\n* Other concomitant infection","ALL","18 Years",{"count":20,"type":21},510,"ESTIMATED","OBSERVATIONAL","Prospective, multicenter, national, observational pharmacological study on the evaluation of efficacy of appropriate monotherapy vs combination treatment for non-complicated Enterococcus faecalis (EF) bloodstream infection (BSI) and identification of gut microbiota fingerprint of patients with EF-BSI correlated to antimicrobial treatment and clinical outcome",[25,26,27],"Enterococcus Faecalis Infection","Blood Stream Infection","Gut Microbiomes",[29,30,31,32],"Enterococcus faecalis bloodstream infection","Human tissue analysis in vitro","Gut microbiota analysis","Enterococcus faecalis genomic analysis","RECRUITING","2025-11-26",{"date":36,"type":37},"2025-12-03","ACTUAL",{"date":39,"type":37},"2021-02-06",{"date":41,"type":21},"2026-09-26",{"name":43,"class":44},"IRCCS Azienda Ospedaliero-Universitaria di Bologna","OTHER",4,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":53,"minAge":18,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":56,"phases":57,"briefSummary":59,"conditions":60,"keywords":4,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":4},"100578765","phase-3-an-open-clinical-trial-of-the-safety-and-efficacy-of-the-drug-fluorothiazinone-300-mg-tablets-with-the-participation-of-adult-patients-with-chronic-bacterial-cystitis-100578765","NCT06815549","An Open Clinical Trial of the Safety and Efficacy of the Drug Fluorothiazinone, 300 Mg Tablets with the Participation of Adult Patients with Chronic Bacterial Cystitis\"","An Open Clinical Trial of the Safety and Efficacy of the Drug Fluorothiazinone, 300 Mg Tablets (Gamaleya Research Institute of Epidemiology and Microbiology, Health Ministry of the Russian Federation) with the Participation of Adult Patients with Chronic Bacterial Cystitis\"","Inclusion Criteria:\n\n1. Patient's written consent to participate in the study in accordance with the current legislation.\n2. The ability to understand the requirements for the study participants, the willingness to follow the procedures according to the Study Protocol.\n3. Female Patients, at least 18 years old.\n4. Ambulatory treatment, absence of indications for emergency hospitalization during the period of inclusion in the study for the infection under study.\n5. Bacterial cystitis, a history of chronic recurrent bladder infection.\n6. The presence of symptoms characteristic of exacerbation of chronic cystitis: pain syndrome (pain in the lower abdomen, when urinating), dysuric symptoms (frequent urination, pain or burning when urinating, imperative urge to urinate, feeling of incomplete emptying of the bladder). 6 points or higher when assessing the characteristic symptoms on the ACSS scale.\n7. Consent of patients with preserved reproductive potential to use effective methods of contraception using one of the following methods: abstinence, intrauterine device, oral\u002F injectable contraceptive, subcutaneous implant or double barrier method (condom with local contraceptive) for the period of participation in the study.\n8. Negative pregnancy test result before randomization for female patients with preserved reproductive potential.\n\nExclusion Criteria:\n\n1. Inability to read in Russian; inability or unwillingness to understand the essence of the research. Any other conditions that limit the validity of obtaining informed consent or may affect the volunteer's ability to participate in the study.\n2. Participation in any other study in the last 90 days;\n3. Presence of an infection of another organ other than a bladder infection, such as endocarditis, osteomyelitis, abscess, meningitis, pneumonia, etc.\n4. Symptoms requiring hospitalization (macrohematuria, concomitant diseases that complicate the course of the disease).\n5. Cystocele of 3-4 degrees.\n6. Treatment with Nitrofurantoin for 30 days before randomization.\n7. Mental illness (registered by a psychiatrist according to medical records).\n8. Treatment with hormonal drugs (with the exception of hormonal contraceptives, hormone replacement therapy, topical medications) for the last 10 days.\n9. Autoimmune diseases or systemic connective tissue diseases in the anamnesis, requiring the appointment of immunosuppressive therapy.\n10. Recipients of solid organs or tissues (bone marrow or peripheral blood stem cells).\n11. Taking immunosuppressive drugs and\u002For immunomodulators for 6 months prior to the start of the study.\n12. The presence of congenital or acquired immunodeficiency (AIDS, etc. according to medical history).\n13. History of malignant neoplasms, with the exception of basal cell or squamous cell epithelial carcinomas of the skin, which were removed without signs of metastasis more than 3 years ago.\n14. Blood donation (450 ml or more of blood or plasma) less than 2 months before the start of the study.\n15. Planned hospitalization and \u002F or surgical intervention during the period of participation in the study, as well as 4 weeks before the expected date of drug administration.\n16. The presence of a concomitant disease that may affect the evaluation of the results of the study or which, in the opinion of the investigator, will not allow the patient to participate in the study or may affect the conduct of the study and \u002F or its results (including the assessment of safety parameters), any conditions that, in the opinion of the medical investigator, may be a contraindication to participating in the study.\n17. Pregnancy or breast-feeding.\n18. Taking any long-acting systemic antibiotic (i.e., with a frequency of administration no more than once a day) for less than 12 hours before randomization.\n19. The need at the time of randomization for additional systemic antimicrobial therapy (including antibacterial, antifungal therapy) other than treatment with the investigational drug, with the exception of a single oral administration of any antifungal drug for the treatment of vaginal candidiasis.\n20. Lactose intolerance, lactase deficiency or glucose-galactose malabsorption, allergy to the components of the studied drug \u002F reference drug in the anamnesis.\n21. Contraindications to the use of Nitrofurantoin (severe renal excretory function disorders, renal insufficiency, oliguria, glucose-6-phosphate dehydrogenase deficiency, hypersensitivity to Nitrofurantoin, stage II-III heart failure, liver cirrhosis, chronic hepatitis, acute porphyria).","FEMALE",{"count":55,"type":21},280,"INTERVENTIONAL",[58],"PHASE3","This study is designed to evaluate the safety, clinical efficacy and antibacterial activity of the drug Fluorothiazinone, 300 mg tablets, (Gamaleya Research Institute of Epidemiology and Microbiology, Health Ministry of the Russian Federation) in the mode of antibacterial monotherapy with the participation of adult patients with chronic bacterial cystitis.\n\nThe main objectives of this study are:\n\n1. To evaluate the safety of the use of the drug Fluorothiazinone according to the indicators\n\n   1. adverse events\u002Freactions;\n   2. serious adverse events\u002Freactions;\n   3. deviations from clinical and laboratory parameters.\n2. To evaluate the therapy effectiveness:\n\n   1. clinical cure - complete resolution or improvement of the signs and symptoms of chronic cystitis that were present at baseline and the absence of new symptoms requiring antimicrobial therapy on days 7, 14 and 28 after the start of therapy;\n   2. the timing of the disappearance of symptoms according to the patient's subjective feelings;\n   3. microbiological response when comparing pre-treatment and post-treatment cultures;\n   4. changes on VAS (visual analogue scale) for pain intensity determination;\n   5. changes on PUF (Pelvic pain and urgency\u002Ffrequency patient symptom scale) for assessing symptoms by patients;\n   6. changes on ACSS (acute cystitis symptom scale);\n   7. development of relapses within 90 days after the start of therapy.\n3. To collect clinical isolates of pathogens for molecular genetic analysis. The identification of DNA and the determination of the bacterial genotype will allow us to assess the microbiological outcomes such as relapse or reinfection.\n4. To determine the sensitivity of the obtained isolates to antibiotics.",[61,62,63,64,25,65],"P. Aeruginosa","Baumannii","Klebsiella Pneumonia","E.coli Infections","Chronic Bacterial Cystitis","NOT_YET_RECRUITING","2025-02-03",{"date":69,"type":37},"2025-02-07",{"date":71,"type":21},"2025-02-17",{"date":73,"type":21},"2025-12-31",{"name":75,"class":44},"Gamaleya Research Institute of Epidemiology and Microbiology, Health Ministry of the Russian Federation",{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":81,"acronym":4,"eligibilityCriteria":82,"healthyVolunteers":83,"sex":17,"minAge":84,"maxAge":85,"enrollmentInfo":86,"targetDuration":4,"studyType":56,"phases":88,"briefSummary":90,"conditions":91,"keywords":94,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":105,"locationsCount":107},"100557061","antimicrobial-efficacy-of-nano-based-icm-on-ef-100557061","NCT06533215","Antimicrobial Efficacy of Nano-Based ICM on E.F","Antimicrobial Efficacy of Nano-Based Intracanal Medications on Enterococcus Faecalis","Inclusion Criteria:\n\n* Single rooted, single canal premolar teeth.\n* Teeth indicated for non-surgical root canal retreatment.\n* Teeth have signs and\u002For symptoms of post-treatment disease manifested by recurrent acute and\u002For chronic periapical abscess.\n* Teeth have clinical signs and symptoms of endodontic failure as sensitivity to percussion, pain, swelling or fistula.\n* Teeth with radiographic features of endodontic failure as persistent periapical lesion or widening of periodontal ligament.\n* Symptomatic or asymptomatic teeth with short root canal filling indicated for prosthetic restoration\n\nExclusion Criteria:\n\n* Patients with any systemic diseases.\n* Pregnant or lactating patients.\n* Immunocompromised patients.\n* Non-restorable tooth.\n* Calcified root canal.\n* Teeth with root fracture.\n* Teeth with periodontal pocket deeper than 4mm.\n* Teeth have procedural error like ledge, broken instrument, or perforation",true,"19 Years","60 Years",{"count":87,"type":21},30,[89],"NA","This in-vivo study aims to evaluate the antimicrobial effect of nano based intracanal medications (Triple antibiotic-loaded chitosan nanoparticles and chlorohexidine loaded by silver nanoparticles) on Enterococcus faecalis count reduction in secondary endodontic infection cases.",[25,92,93],"Endodontically Treated Teeth","Endodontic Disease",[95,96,97],"intracanal medication","Enterococcus Faecalis","secondary endodontic infection cases.","2024-07-30",{"date":100,"type":37},"2024-08-01",{"date":102,"type":37},"2024-01-02",{"date":104,"type":21},"2025-03-02",{"name":106,"class":44},"Tanta University",1]