Table 1 Intervention description
Groups | Interventions |
|---|---|
Experimental group | Patients in this arm will receive study medication fosfomycin 500 mg every 8 h orally or intravenously in case of intolerance to the oral route |
Control group | Ciprofloxacin 500 mg every 12 h orally or intravenously in case of intolerance to the oral route (https://clinicaltrials.gov/study/NCT01371656?term=ACCL0934&rank=1) |