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Completed

NCT Number: NCT03228108

Culture-guided Antimicrobial Prophylaxis in Men Undergoing Prostate Biopsy.

This study aims to assess the effectiveness and cost-effectiveness of rectal swab culture-guided antimicrobial prophylaxis to reduce infectious complications after transrectal prostate biopsy. Half of participants will receive routine empirical prophylaxis with oral ciprofloxacin (control group), while the other half will receive rectal culture-guided oral antibiotic prophylaxis (intervention group). In the intervention group, men whose rectal swabs do not show ciprofloxacin-resistant bacteria will receive ciprofloxacin prophylaxis, comparable to the control group. In case of ciprofloxacin-resistant bacteria an alternative oral antibiotic based on the culture results will be prescribed (trimethoprim/sulfamethoxazole, fosfomycin or pivmecillinam/augmentin).

The investigators hypothesise that the targeted prophylaxis group (intervention group) will have a lower rate of post-biopsy infectious complications compared to the control group.

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Key information

Age range

18 year–90 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 4

Primary location

Jeroen Bosch Hospital, 's-Hertogenbosch, Netherlands

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About this study

Several classes of antibiotics are proven effective for prophylaxis during transrectal prostate biopsy, reducing infectious complications to less than 1% in case of susceptible rectal flora. Ciprofloxacin has been best studied and is recommended as first choice prophylaxis in urology guidelines. However, due to increasing fluoroquinolone resistance in gram negative bacilli (currently more than 20% in E.coli), a significant increase up to 6% in infectious complications after transrectal prostate biopsy was recently noticed. Antibiotic treatment of these infections and hospitalization may account for increased health care associated costs and will contribute to the further development of antibiotic resistance.

Besides, in urology guidelines no clear recommendations are made on the duration of prophylaxis. In the Netherlands, therefore, various prophylactic ciprofloxacin schedules are used, of which 2 to 3 day regimens are most common. Prolonged duration of prophylaxis during prostate biopsy is not proven to be more effective than a 1-day regimen, but it is more likely to select more fluoroquinolone (FQ) resistance.

This study aims to assess the effectiveness and cost-effectiveness of rectal culture-guided antimicrobial prophylaxis to reduce infectious complications after transrectal prostate biopsy. Also, duration of antibiotic prophylaxis will be minimized to 24 hours, thereby controlling further development of resistant bacteria.

The culture method used in this study with four phenotypic screening agars to support the choice of one of the oral prophylactic antibiotics is innovative. Culture results become available rapidly, within 48 hours, the method is simple, relatively inexpensive, as it does not need full susceptibility testing of separate colonies, and useful in daily practice.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subject is able and willing to sign the Informed Consent Form.
  • Subject undergoes a transrectal prostate biopsy as part of the standard care in the Radboudumc (Nijmegen), Canisius Wilhelmina hospital (Nijmegen) or Catharina hospital (Nijmegen) (because of suspicion of prostate cancer).

Exclusion criteria

  • Inability to receive ciprofloxacin (e.g. documented history of sensitivity to medicinal products or excipients similar to those found in the antibiotic prophylaxis, relevant history or presence of cardiovascular disorders)
  • Inability to receive either co-trimoxazole, fosfomycin and pivmecillinam/augmentin prophylaxis for any reason (e.g. documented history of sensitivity to medicinal products or excipients similar to those found in the antibiotic prophylaxis)
  • Inability to understand the nature of the trial and the procedures required.
  • Individuals with an urinary tract infection or acute prostatitis within 14 days prior to intervention.
  • Individuals who receive antibiotics within 14 days before prostate biopsy.
  • Individuals who fail to send a rectum swab to the microbiology laboratory.
  • Individuals whose rectal swab shows no growth on a (growth) control MacConkey agar without antibiotics.

Treatment and study plan

Ciprofloxacin

Drug

see study arms.

Other names: Ciproxin

trimethoprim/sulfamethoxazole

Drug

see study arms.

Other names: Co-trimoxazole

Fosfomycin

Drug

see study arms.

Other names: Monuril

Pivmecillinam/augmentin

Drug

see study arms.

Other names: Selexid, Amoxicillin/clavulanic acid

Primary outcomes

  1. Any registered clinical infectious complication after prostate biopsy

    Time frame: within 7 days post-biopsy

    Urinary tract infection, pyelonephritis, sepsis, fever, acute prostatitis, acute epididymitis

Secondary outcomes

  1. Cost of care

    Time frame: within 30 days after prostate biopsy

    Difference of costs between the intervention and the control group

  2. Positive microbiological results

    Time frame: within 7 and 30 days after prostate biopsy

    Urine or blood culture results

  3. Any registered clinical infectious complication after prostate biopsy

    Time frame: within 7 and 30 days after prostate biopsy

    Urinary tract infection, pyelonephritis, sepsis, fever, acute prostatitis, acute epididymitis

  4. Hospitalization after prostate biopsy

    Time frame: within 30 days after prostate biopsy

    Any hospital admission, including ICU admission

  5. Overall mortality

    Time frame: within 30 days after prostate biopsy

    Mortality of any cause

  6. Side effects of used antibiotics

    Time frame: within 30 days after prostate biopsy

    All side effects mentioned in the Summary of Product Characteristics (SPC)

  7. Prevalence of ciprofloxacin-resistant gram negative bacilli in local rectal flora

    Time frame: rectal swabs are taken 14 days before biopsy

    Assessed through microbiological rectal swab cultures

  8. Overall antibiotic use after prostate biopsy

    Time frame: within 30 days after prostate biopsy

    Number of antibiotic prescriptions

Sponsors and collaborators

Lead sponsor

Radboud University Medical Center

Other

Collaborators

  • ZonMw: The Netherlands Organisation for Health Research and Development

Registry information

Official study title

The Effect of Rectal Swab Culture-guided Antimicrobial Prophylaxis in Men Undergoing Prostate Biopsy on Infectious Complications and Cost of Care: A Randomized Controlled Trial in the Netherlands.

Acronym: pro-SWAP

Important dates

Study start
2018
Primary completion
2021
Study completion
2021
First posted
Jul 24, 2017
Registry last updated
May 10, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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