Potentiated Aminoglycosides in Postoperative Urinary Tract Infection Prophylaxis

Urinary Tract Infections Clinical Trial

— UROPOT  

Official title:

Metabolic Potentiation of Aminoglycosides: a Novel Antimicrobial Strategy to Prevent Urinary Tract Infections (UROPOT TRIAL).

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05761405
• Other study ID #: 2022-001979
• Status: Recruiting
• Phase: Early Phase 1
• Start date: January 16, 2024
• Est. completion date: April 15, 2026

Study information

• Verified date: February 2024
• Source: Centre Hospitalier Universitaire Vaudois
• Contact: Sylvain Meylan, MD-PhD
• Phone: +41795569418
• Email: sylvain.meylan[@]chuv.ch
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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).

Description:

UROPOT is a randomized, single-centre, double-blind, pilot trial comparing a combination of aminoglycosides and mannitol to standard of care or aminoglycosides alone for the peri-operative antimicrobial prophylaxis of endourological procedures with mucosal trauma in the presence of hardware. Adults (≥18 years) scheduled for such procedures with mucosal trauma (stone surgery with hardware, pig-tail catheter exchanges) and having an asymptomatic bacteriuria E. coli or K. pneumoniae as identified 10 days prior to surgery, will be randomly assigned (1:1:1) to receive standard prophylaxis (gen. Ceftriaxone 2 g) for 24 hours, a single dose of amikacin (6mg/kg i.v.) or a single dose of mannitol (pres. 2.5g i.v. bolus)/amikacin (3mg/kg i.v.). Sample size for the three groups will be constructed to demonstrate a non-inferiority for the clinical outcome (absence of infectious complication within 48 hours from operation) with a power of 80%. Complications in the absence of antimicrobial prophylaxis range from 2-10%. Patients will be excluded if baseline urine culture has another bacterial pathogen or E. coli or K. pneumoniae are documented to be aminoglycoside resistant. The primary endpoint will be the prevention of complications(clinical) that will be evaluated for non-inferiority compared to the accepted standard of care. i.e., within a 6% margin Assuming a rate of complication as low as 2%, the new treatments will be considered non-inferior if the corresponding rate of complication is not above 8% (i.e., 6% margin). This non-inferiority margin can be evaluated with a total for 128 patients per treatment arm, at 1-sided alpha of 5%, with power 80%, through an exact two-sample test for proportions. Two comparisons will be performed of arm A and of arm B versus standard of care (SoC). In addition, a microbiological outcome will be included to document higher biofilm eradication rate. This will be documented by sonication of extracted hardware as well as repeat urine culture at post-operative days 7 and 14 days (secondary outcomes). Safety will be monitored with a specific focus on nephrotoxicity and ototoxicity. If highly efficient, this novel antimicrobial strategy would be expanded to treatment of complicated urinary tract infections.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 90
• Est. completion date: April 15, 2026
• Est. primary completion date: October 15, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Written informed consent

• Adults (=18 years)

• Ureteral stent in situ

• Patients scheduled for endourological ureteral manipulations (e.g. endourological stone surgery, ureteral stent exchange)

• Asymptomatic bacteriuria with strains of E. coli and/or K. pneumoniae sensitive to Ceftriaxone and Amikacin/Aminoglycosides.

Exclusion Criteria:

• Allergy to one of the study drugs Beta-lactams, aminoglycosides or mannitol

• Pregnant and lactating women

• Glomerular filtration rate (CKD-EPI eGFR) < 50ml/min / 1,73m2

• Hearing impairment

• Myasthenia gravis or other forms of myoneural disorders

• Congestive heart failure, Pulmonary edema

• Intracranial hemorrhage, blood-brain barrier compromise

• Previous (within 3 months prior to randomization) or concomitant participation in another interventional clinical trial

• Antibiotic treatment within 14 days prior to randomization

• Mixed cultures of E. coli and/or K. pneumonia with other bacteria

• Inability to understand and follow the protocol

• Inability to give informed consent

• BMI<20 or >30

Related Conditions & MeSH terms

• Communicable Diseases
• Infections
• Urinary Tract Infections
• Urological System Complication of Procedure

Intervention

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.
• 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.

Locations

Country	Name	City	State
Switzerland	CHUV	Lausanne

Sponsors (3)

Lead Sponsor	Collaborator
Centre Hospitalier Universitaire Vaudois	Ecole Polytechnique Fédérale de Lausanne, Insel Gruppe AG, University Hospital Bern

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Infection prophylaxis	Incidence of postoperative infections within the initial 48 hours postoperatively.	48 hours postoperatively
Secondary	Combined microbiological eradication	anti-biofilm activity as determined by culture of sonicated catheter (CFU/ml) and intraoperative urine culture (CFU/ml)	6-8 hours post infusion
Secondary	Sustained microbiological eradication	To document eradication of bacteriuria at postoperative day 2 and 14 day by urine culture (CFU/ml)	Up to 2 weeks
Secondary	Surgical safety outcome	Postoperative complications	Day 0-14
Secondary	Pharmacokinetics outcome	Measurements of maximum urine drug concentrations (Amikacin, Ceftriaxone, Mannitol)	Day 0, Day 2, Day 14
Secondary	Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]	Safety and tolerability of Amikacin/Mannitol combination (serious adverse events (SAEs), pre-specified adverse events (AEs) of special interest (ototoxicity, nephrotoxicity).	Day 0-Day 14