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Tundra lists 3 Enterococcus Faecalis Infection clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.
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NCT06833593
Antimicrobial Combination Therapy for Treatment of Enterococcus Faecalis Bacteremia
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
Gender: All
Ages: 18 Years - Any
Updated: 2025-12-03
3 states
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"
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. The main objectives of this study are: 1. To evaluate the safety of the use of the drug Fluorothiazinone according to the indicators 1. adverse events/reactions; 2. serious adverse events/reactions; 3. deviations from clinical and laboratory parameters. 2. To evaluate the therapy effectiveness: 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; 2. the timing of the disappearance of symptoms according to the patient's subjective feelings; 3. microbiological response when comparing pre-treatment and post-treatment cultures; 4. changes on VAS (visual analogue scale) for pain intensity determination; 5. changes on PUF (Pelvic pain and urgency/frequency patient symptom scale) for assessing symptoms by patients; 6. changes on ACSS (acute cystitis symptom scale); 7. development of relapses within 90 days after the start of therapy. 3. 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. 4. To determine the sensitivity of the obtained isolates to antibiotics.
Gender: FEMALE
Ages: 18 Years - Any
Updated: 2025-02-07
NCT06533215
Antimicrobial Efficacy of Nano-Based ICM on E.F
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.
Gender: All
Ages: 19 Years - 60 Years
Updated: 2024-08-01