Potentiated Aminoglycosides in Postoperative Urinary Tract Infection Prophylaxis
NCT05761405 · Status: RECRUITING · Phase: EARLY_PHASE1 · Type: INTERVENTIONAL · Enrollment: 90
Last updated 2024-02-08
Summary
Urinary tract hardware such as pig-tail catheters are are frequently used for management of urolithiasis or other obstructive pathologies. They are readily colonized by urogenital flora leading to asymptomatic bacteriuria. While asymptomatic bacteriuria is not per se a problem for patients, it may lead to severe infections in the context of hardware manipulation leading to mucosal damage (e.g. catheter exchanges or stone extraction). Such interventions therefore warrant an antibiotic prophylaxis. However, bacteria rapidly form biofilms on hardware; aside of fluoroquinolones, antibiotics have limited anti-biofilm activity. Furthermore, the widespread use of antibiotics has lead to resistant strains. Hence, novel antimicrobial strategies are needed. Recently, metabolism-based potentiation of aminoglycoside has shown high antimicrobial activity against persistent forms of bacteria such as biofilms in the context of murine catheter-associated urinary tract infections. Because of the highly favorable pharmacodynamic profile of aminoglycoside in the urinary tract and the metabolic potentiation, aminoglycosides can be reduced to levels with minimal toxicity.
UROPOT aims to compare the efficacy of potentiated aminoglycoside to standard of care for (i) prophylaxis of asymptomatic bacteriuria during urinary hardware manipulations with mucosal trauma (Pig-tail catheter exchange, stone surgery with prior in-dwelling catheter, etc.) and (ii) sustained microbiological eradication through antibiofilm activity. UROPOT will compare the rate of post-interventional urinary tract infections (primary outcome). It will also assess safety and eradication potency (microbiological outcome).
Conditions
- Urinary Tract Infections
- Urological System Complication of Procedure
Interventions
- COMBINATION_PRODUCT
-
mannitol-enhanced aminoglycoside
Preselected patients with ureteral stents in situ who are scheduled to undergo endourological ureteral stent manipulation will have routine urine cultures prior to intervention. Procedures: Consented patients will be randomized for the type of antibiotic prophylaxis according to a global randomization list (i.e. CRO, AMK, AMK1/2+MAN)). Antibiotics (± mannitol) will be delivered in a single infusion that will be administered within 30 minutes.
- DRUG
-
Ceftriaxon
Preselected patients with ureteral stents in situ who are scheduled to undergo endourological ureteral stent manipulation will have routine urine cultures prior to intervention. Procedures: Consented patients will be randomized for the type of antibiotic prophylaxis according to a global randomization list (i.e. CRO, AMK, AMK1/2+MAN)). Antibiotics will be delivered in a single infusion that will be administered within 30 minutes.
- DRUG
-
Amikacin
Preselected patients with ureteral stents in situ who are scheduled to undergo endourological ureteral stent manipulation will have routine urine cultures prior to intervention.
Sponsors & Collaborators
-
Ecole Polytechnique Fédérale de Lausanne
collaborator OTHER -
Insel Gruppe AG, University Hospital Bern
collaborator OTHER -
Centre Hospitalier Universitaire Vaudois
lead OTHER
Principal Investigators
-
Sylvain Meylan · Centre Hospitalier Universitaire Vaudois
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-01-16
- Primary Completion
- 2025-10-15
- Completion
- 2026-04-15
Countries
- Switzerland
Study Locations
More Related Trials
-
Patient Satisfaction and Long-term Safety of Intravesical Aminoglycoside Instillations in UTI Prevention
NCT05376670 ·Status: COMPLETED
-
Single Dose Aminoglycosides for Acute Uncomplicated Cystitis in the Emergency Department Setting
NCT05702762 ·Status: UNKNOWN ·Phase: PHASE2
-
A Pilot Comparison of Short-course Nitrofurantoin in Females With Uncomplicated Bacterial Cystitis in the Emergency Department
NCT01749605 ·Status: COMPLETED ·Phase: PHASE4
-
Diagnosis, Antibiotic Prescribing Practices and Outcomes of cUTI in an Outpatient Setting
NCT05091931 ·Status: COMPLETED
-
Can Probiotics be Used in the Prevention of Recurrent UTI in Paediatric Neurogenic Bladder
NCT02044965 ·Status: UNKNOWN ·Phase: PHASE1/PHASE2
-
Nitrofurantoin and Urinary Tract Infections (UTIs)
NCT00678041 ·Status: TERMINATED ·Phase: NA
-
Comparative Study to Evaluate Efficacy and Safety of Gepotidacin to Nitrofurantoin in Treatment of Uncomplicated Urinary Tract Infection (UTI)
NCT04187144 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Evaluate Efficacy and Safety of Gepotidacin in the Treatment of Uncomplicated Urinary Tract Infection (UTI)
NCT04020341 ·Status: COMPLETED ·Phase: PHASE3
-
Intravesical Gentamicin to Prevent Recurrent UTI
NCT06332781 ·Status: COMPLETED ·Phase: PHASE4
-
Safety and Efficacy of a Weekly Oral Cyclic Antibiotic Programme in the Prevention of Urinary Tract Infection on Neurological Bladder
NCT01388413 ·Status: COMPLETED ·Phase: PHASE4
-
Gentamicin Bladder Instillation in Individuals With Spinal Cord Injury Having Chronic Urinary Tract Infections
NCT03931408 ·Status: COMPLETED ·Phase: PHASE2
-
Prophylactic Antibiotics for Urinary Tract Infections After Robot-Assisted Radical Cystectomy
NCT04502095 ·Status: COMPLETED ·Phase: PHASE4
-
Study of the Pharmacokinetics of Ceftriaxone
NCT07169097 ·Status: RECRUITING
-
Suppressive Therapy With Oral Antibiotics for Prevention of Postoperative Urinary Tract Infection (UTI)
NCT01450800 ·Status: COMPLETED ·Phase: PHASE4
-
Antibiotic Prophylaxis for Bladder Botox
NCT04444440 ·Status: RECRUITING ·Phase: PHASE4
-
Improving Antibiotic Prescribing for Urinary Tract Infections in Frail Elderly
NCT03970356 ·Status: COMPLETED ·Phase: NA
-
Controlling Antimicrobial Use Through Reducing Unnecessary Treatment of Catheter Associated Urinary Tract Infections
NCT02650518 ·Status: UNKNOWN ·Phase: PHASE2/PHASE3
-
Clinical Trial Testing Whether Targeted Antibiotic Prophylaxis Can Reduce Infections After Cystectomy Compared to Empiric Prophylaxis
NCT06709196 ·Status: RECRUITING ·Phase: PHASE4
-
Assessment of UTI Symptoms and Quality of Life According to Antibiotics Treatment in Acute Uncomplicated Cystitis
NCT01631955 ·Status: COMPLETED
-
Analysis of Bacterial Multidrug Tolerance in Patients Prone to Urinary Tract Infections
NCT06724588 ·Status: ENROLLING_BY_INVITATION
-
Efficacy of Ciprofloxacin for the Treatment of Uncomplicated Urinary Tract Infection (uUTI)
NCT03366207 ·Status: COMPLETED ·Phase: PHASE4
-
The Urinary Microbiome in Patients Receiving Intradetrusor Botox Injections
NCT04479709 ·Status: COMPLETED
-
INtravesical Antimicrobial Agents v STANDard Oral Antibiotics for the Treatment of Acute UTI in Women With rUTI
NCT03299387 ·Status: WITHDRAWN ·Phase: PHASE4
-
Antibiotic Strategy and Asymptomatic Bacteriuria in the Context of Intra-vesical Botulinum Toxin A Injections.
NCT05534399 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Study of E. Coli Isolates From Recurrent Urinary Tract Infections
NCT05826067 ·Status: RECRUITING