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Comparison · NCT01659866-deaths

Cipro-susceptible vs Cipro-resistant: deaths from any cause

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Cipro-susceptible vs Cipro-resistant: deaths from any cause. Trial comparisons, record NCT01659866-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01659866-deaths

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 1000.00885wilson
Risk in group 2000.0458wilson
Risk difference, group 1 minus group 20-0.04580.00885newcombe hybrid score
Risk ratio, group 1 over group 2loga group has no participants with the outcome
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to harmfrom the risk difference intervalthe two groups' risks are equal

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Cipro-susceptible
Patients with ciprofloxacin-susceptible bacteria on their rectal swab cultures will receive ciprofloxacin, the standard of care, as prophylaxis for their prostate biopsy~Ciprofloxacin: 500 mg orally 2 hours before prostate biopsy
0430EG000
Group 2Cipro-resistant
Patients with ciprofloxacin-resistant bacteria on their rectal swab will receive one of the following drugs:~* trimethoprim-sulfamethoxazole 1 double strength tablet orally 2 hours before the procedure and again 12 hours later~* cefuroxime 500 mg orally 2 hours before the procedure then again 12 hours later~* ceftriaxone 500 mg intramuscularly 2 hours before the procedure~* gentamicin 2mg/kg intramuscularly 2 hours before the procedure~* amikacin 5 mg/kg intramuscularly 2 hours before the procedure~* aztreonam 500 mg intramuscularly 2 hours before the procedure~* imipenem 500 mg intramuscularly 2 hours before the procedure~* ceftriaxone 2000 mg intravenously 1 hour before the procedure~* gentamicin 2 mg/kg intravenously 1 hour before the procedure~* amikacin 5mg/kg intravenously 1 hour before the procedure~* aztreonam 2000 mg intravenously 1 hour before the procedure~* imipenem 1000 mg intravenously 1 hour before the procedure
080EG001

Harm

What it counts
Total, all-cause mortality
Time frame

Source ClinicalTrials.gov

Trial

Title
Antibiotic Prophylaxis for Transrectal Prostate Biopsy
NCT number
NCT01659866
Phases
PHASE4
Conditions
Infection
Interventions
Ciprofloxacin, trimethoprim-sulfamethoxazole, cefuroxime, ceftriaxone, gentamicin, amikacin, aztreonam, imipenem, ceftriaxone, gentamicin, amikacin, aztreonam, imipenem
Lead sponsor
Northwestern University
Results first posted
2019-06-25

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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