Efficacy of Ciprofloxacin for the Treatment of Uncomplicated Urinary Tract Infection (uUTI)

Completed · Phase 4

Conditions studied: UTI - Lower Urinary Tract Infection, Antibiotic Resistant Infection

In brief

This is a prospective, Phase 4, open label, multi-center study of the clinical and microbiologic efficacy of ciprofloxacin for the treatment of uncomplicated urinary tract infections in adult women.

Key facts

Study ID

NCT03366207

Run by

Iterum Therapeutics, International Limited

People needed

250

Starts

2017-12-15

Expected to finish

2018-10-26

Last updated by the study team

2019-09-06

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Female patients ≥18 years of age with more than 24 hours of urinary symptoms attributable to a UTI
• Two of the following signs and symptoms of uUTI: urinary frequency, urinary urgency, pain or burning on micturition, suprapubic pain, gross hematuria
• A mid-stream urine specimen with:
• a dipstick analysis positive for nitrite AND
• a dipstick analysis positive for leukocyte esterase
• Has given written informed consent to participate in the study.

You may not qualify if…

• Presence of signs and symptoms suggestive of acute pyelonephritis: fever (temperature > 38°Celsius), chills, costovertebral angle tenderness, flank pain, nausea and/or vomiting
• Receipt of prior effective antibacterial drug therapy for uUTI for the presenting illness unless the recovered pathogen demonstrates resistance to initial antibiotic and clinical symptoms persist
• Concurrent use of non-study antibacterial drug therapy that would have a potential effect on outcome evaluations in patients with uUTI
• Patients with ileal loops or urinary stoma
• Patients with an indwelling urinary catheter in the previous 30 days
• Patients with paraplegia
• Patients who are likely to receive ongoing antibacterial drug prophylaxis after treatment of uUTI (e.g., patients with vesico-ureteral reflux)
• Any history of trauma to the pelvis or urinary tract
• Patient's urine culture results, if available at study entry, identify more than 2 microorganisms regardless of colony count or patient has a potential fungal pathogen
• Patient's urine culture results, if available at study entry, identifies the causative uropathogen for the presenting illness to be resistant to ciprofloxacin
• Patient has severe chronic kidney disease, or is receiving hemodialysis or peritoneal dialysis or had a renal transplant
• Patient is known to have severe neutropenia
• Patient is known to be pregnant
• Patients with uncontrolled diabetes mellitus
• Patients with a known history of myasthenia gravis
• Patients who require concomitant administration of tizanidine
• Patients with a history of allergy to quinolones
• Patient is considered unlikely to survive the study period or has a rapidly progressive or terminal illness including septic shock which is associated with a high risk of mortality

Where it is running

• Restore Clinical Research — Cary, North Carolina, United States

Full record on ClinicalTrials.gov

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