The optimal duration of antimicrobial prophylaxis (study medication Cotrimoxazole (Trimethoprim/Sulfamethoxazole)) in transurethral resection of the prostate and Greenlight Laser vaporisation of the prostate is investigated by comparing a guideline-conform single-dose prophylaxis (intervention) versus usual clinical care (i.e. 3-day prophylaxis; control) for prevention of urinary tract infections.
Increasing antimicrobial resistance rates have a substantial impact on morbidity, mortality and healthcare costs and is particularly prevalent among urological patients due to an overuse of antimicrobial agents for therapeutical and prophylactic indications. Transurethral resection of the prostate is one of the most frequently performed urological procedures in Switzerland and a single-dose of antimicrobial prophylaxis is recommended to reduce postoperative urinary tract infections. For photoselective vaporisation of the prostate with the Greenlight Laser, a similar operative alternative, there are currently no international guidelines for antimicrobial prophylaxis. The optimal duration of antimicrobial prophylaxis in transurethral resection of the prostate and Greenlight Laser vaporisation of the prostate is investigated by comparing a guideline-conform single-dose prophylaxis (intervention) versus usual clinical care (i.e. 3-day prophylaxis; control) for prevention of urinary tract infections. The study medication Cotrimoxazole (Trimethoprim/Sulfamethoxazole) is a routinely used antimicrobial substance recommended in international and in-house guidelines for antimicrobial prophylaxis and treatment of urinary tract infections. Perioperative antimicrobial prophylaxis will be Cotrimoxazole short infusion in both groups. Postoperative study medication packages consists of either five tablets of placebo or five tablets of Cotrimoxazole (Nopil forte®) 800/160mg using licensed product repacked in a new immediate container which is blinded
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
728
five oral applications of TMP/SMX 800/160 mg (Nopil forte® tablets) at the evening of the surgery and thereafter twice daily on day 1 and 2 after surgery while the patient is in hospital.
five oral applications of Placebo at the evening of the surgery and thereafter twice daily on day 1 and 2 after surgery while the patient is in hospital.
St. Claraspital, Department of Urology
Basel, Canton of Basel-City, Switzerland
Kantonsspital Aarau, Department of Urology
Aarau, Switzerland
University Hospital Basel, Division of Infectious Diseases and Hospital Epidemiology
Basel, Switzerland
Kantonsspital Baselland, Department of Urology
Liestal, Switzerland
Symptomatic UrinaryTract Infection (UTI)
Symptomatic UTI (based on clinical diagnosis) treated with antimicrobial agents
Time frame: within 30 days after randomization
Symptomatic UTI by measured bacteriuria
measured bacteriuria of ≥105 cfu/ml treated with antimicrobial agents (key secondary outcome)
Time frame: within 30 days after randomization
Symptomatic cystitis (based on clinical diagnosis)
Symptomatic cystitis (based on clinical diagnosis)
Time frame: within 30 days after randomization
Symptomatic epididymitis (based on clinical diagnosis)
Symptomatic epididymitis (based on clinical diagnosis)
Time frame: within 30 days after randomization
Symptomatic pyelonephritis (based on clinical diagnosis)
Symptomatic pyelonephritis (based on clinical diagnosis)
Time frame: within 30 days after randomization
Symptomatic prostatitis (based on clinical diagnosis)
Symptomatic prostatitis (based on clinical diagnosis)
Time frame: within 30 days after randomization
Symptomatic urethritis (based on clinical diagnosis)
Symptomatic urethritis (based on clinical diagnosis)
Time frame: within 30 days after randomization
Urosepsis (based on clinical diagnosis)
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University Hospital Zurich, Department of Urology
Zurich, Switzerland
Urosepsis (based on clinical diagnosis)
Time frame: within 30 days after randomization
Prescription of antibiotics (for any reason)
Prescription of antibiotics (for any reason)
Time frame: within 30 days after randomization
Prescribed defined daily doses (DDD) of antibiotics (cumulative sum of DDD) day 30)
Prescribed defined daily doses (DDD) of antibiotics (cumulative sum of DDD)
Time frame: within 30 days after randomization
Asymptomatic bacteriuria of ≥105 cfu/ml treated with antimicrobial agents
Asymptomatic bacteriuria of ≥105 cfu/ml treated with antimicrobial agents
Time frame: within 30 days after randomization
Detection of multidrug-resistant bacteria in Urine culture
Detection of multidrug-resistant bacteria in Urine culture
Time frame: within 30 days after randomization
Any Clostridium difficile-associated infection
Any Clostridium difficile-associated infection
Time frame: within 30 days after randomization
Duration of catheterisation (cumulative sum of days between randomisation and end of catheterisation or day 30)
Duration of catheterisation (cumulative sum of days between randomisation and end of catheterisation or day 30)
Time frame: within 30 days after randomization
Duration of hospital stay (cumulative sum of Hospital days between randomisation and day 30)
Duration of hospital stay (cumulative sum of Hospital days between randomisation and day 30)
Time frame: within 30 days after randomization
Duration of intensive care unit (ICU) stay (cumulative sum of ICU days between randomisation and day 30)
Duration of intensive care unit stay (cumulative sum of ICU days between randomisation and day 30)
Time frame: within 30 days after randomization
Re-hospitalisation (within 30 days after randomisation)
Re-hospitalisation (within 30 days after randomisation)
Time frame: within 30 days after randomization
Change of International Prostate Symptom Score (prior to randomisation and at day 30 after randomisation)
Change of International Prostate Symptom Score (prior to randomisation and at day 30 after randomisation)
Time frame: within 30 days after randomization
Change of Quality of life Score (prior to randomisation and at day 30 after randomisation)
Change of Quality of life Score (prior to randomisation and at day 30 after randomisation)
Time frame: within 30 days after randomization
All-cause mortality
All-cause mortality
Time frame: within 30 days after randomization
Total adverse events
Total adverse events
Time frame: within 30 days after randomization
Total serious adverse events
Total serious adverse events
Time frame: within 30 days after randomization