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Phase 4 N=510 Treatment

Antibiotic Prophylaxis for Transrectal Prostate Biopsy

Infection

Enrolled (actual)
510
Serious AEs
0.0%
Results posted
Jun 2019
Primary outcome: Primary: Number of Participants With Post-biopsy Infection. — 6; 3 participants — p=<0.05

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Ciprofloxacin (Drug); trimethoprim-sulfamethoxazole (Drug); cefuroxime (Drug); ceftriaxone (Drug); gentamicin (Drug); amikacin (Drug); aztreonam (Drug); imipenem (Drug)
Age
Adult, Older Adult · 30+ yrs
Sex
Male
Sponsor
Northwestern University
Primary completion
Aug 2015

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Post-biopsy Infection.
6; 3 <0.05 sig

Summary

This study is being conducted in men scheduled to undergo transrectal ultrasound-guided prostate biopsy (TRUSP). Traditionally prior to prostate biopsy, an antibiotic, ciprofloxacin, has been given to men to prevent biopsy-related infections. In recent years as ciprofloxacin resistance has increased in the community, more and more men are becoming infected with ciprofloxacin-resistant bacteria after prostate biopsy. This study is being done to determine if obtaining rectal swab cultures and choosing antibiotics based on these culture results will result in fewer infectious complications than giving all men ciprofloxacin. The investigators will compare 2 groups: men whose rectal swabs do not show ciprofloxacin-resistant bacteria will receive ciprofloxacin prior to biopsy, and men whose swabs do show ciprofloxacin-resistant bacteria will receive alternative antibiotics based on their culture results. Our hypothesis is that these 2 groups will have equal numbers of post-biopsy infectious complications and both groups will have fewer infectious complications than a historical group who received empiric ciprofloxacin without the benefit of rectal swab culture results.

Eligibility Criteria

Inclusion Criteria

  • Ability and willingness to provide written informed consent.
  • All individuals who will undergo TRUSP as part of their standard of care are eligible for study.

Exclusion Criteria

  • Men under 30 years of age
  • Individuals whose rectal swab indicates that they harbor CS-GNB who cannot receive ciprofloxacin as pre-procedure prophylaxis for any reason
  • Individuals whose rectal swab indicates that they harbor CR-GNB who cannot abide by the antimicrobial prophylaxis guidelines outlined in the study protocol for any reason
  • Individuals who do not wish to complete the pre-procedure risk factor questionnaire or the two post-procedure phone questionnaires to assess for infectious complications
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01659866). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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