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Phase 2 Completed N=134 Randomized Single-blind Prevention

Effectiveness of Preurodynamic With Posturodynamic Levofloxacin on the Incidence of UTI

Source: ClinicalTrials.gov NCT05219877 ↗
Enrolled (actual)
134
Serious AEs
1.5%
Results posted
Nov 2023
Primary outcomePrimary: Number of Participant With Urinary Tract Infection — 12; 13 Participants

Summary

This study aims to compare the effectiveness of preoperative single dose of levofloxacin with postoperative levofloxacin for three days on the incidence of urinary tract infections (UTI) after urodynamic examination.

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participant With Urinary Tract Infection
12; 13

Eligibility Criteria

Inclusion Criteria

  • Male/female patients > 18 years who have indications for urodynamics
  • Willing to participate in research

Exclusion Criteria

  • Allergy to levofloxacin
  • History of taking antibiotics in 1 month • Pregnant
  • Uncontrolled DM
  • Use a urinary catheter
  • Having a UTI before urodynamics, based on clinical symptoms and urine examination results
  • Refuse to participate in research
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05219877). 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. Informational only — not medical advice.

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