Trial to Evaluate the Efficacy and Safety of Cipro® XR in Treating Female Patients With Lower Urinary Tract Infections

• Status: Completed
• Trial end date: 2003-10-01
• Target enrollment: 0
• Participant gender: Female

Summary

This trial evaluated how effective and safe Cipro XR was in treating female patients with signs and symptoms of a lower urinary tract infections. After 3 days of treatment, patients were evaluated to determine if signs/symptoms disappeared and the infecting bacteria was eliminated.

• Phase: Phase 4
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Bayer
• Treatments: Ciprofloxacin

Criteria

Inclusion Criteria:

• Non-pregnant, non-lactating female outpatients between the ages of 18 - 44 years (inclusive)

• Patients with at least two of the following clinical signs and symptoms of an uUTI:

• Dysuria

• Frequency

• Urgency

• Suprapubic pain

• Patients with onset of symptoms < 72 hours prior to study entry

• Patients with one positive pre-treatment clean-catch midstream urine culture at enrollment in the study, defined as > 10000 CFU/mL (study drug treatment is permitted prior to the availability of urine culture results)

• Positive leukocyte esterase (LE) (1+ or greater) utilizing a urine dipstick method of analysis

• Patients willing to give written informed consent

• Cultures must be performed on pre-treatment clean-catch midstream urine (MSU) specimens

Exclusion Criteria:

• Males

• Women who are pregnant, nursing, or not using two medically accepted, effective methods of birth control

• Patients with known or suspected hypersensitivity to quinolones

• Patients unable to take oral medication for any reason

• Patients with an asymptomatic bacteriuria

• Patients with complicated UTI, defined as: a clinical syndrome characterized by the development of systemic and local signs and symptoms of fever (> 38.3°C/101°F orally), chills, malaise, flank pain, back pain, or costovertebral angle (CVA) pain or tenderness

• Symptoms as outlined in the inclusion criteria occurring in the presence of a functional or anatomical abnormality of the urinary tract or in the presence of urinary catheterization

• Patients with symptoms of a UTI within the 4 weeks prior to the present episode

• Patients with the onset of symptoms >72 hours prior to study entry

• Patients with three or more episodes of any UTI in the past 12 months

• Patients with evidence of factors predisposing to the development of UTIs, including calculi, stricture, primary renal disease (e.g. polycystic renal disease), or neurogenic bladder

• Patients who received systemic antimicrobial therapy within 48 hours prior to entry

• Patients with a neutrophil count < 1000/mm3, CD4 < 200/mm3 or other conditions associated with significant depression in host defense; HIV testing is not mandatory

• Patients requiring concomitant systemic antibacterial therapy with agents not specified in this protocol

• Patients with a previous history of tendinopathy associated with fluoroquinolones

• Patients diagnosed with a rapidly fatal underlying disease (death expected within six months)

• Patients requiring concomitant use of theophylline

• Patients previously enrolled in this clinical study

• Patients taking an investigational drug in the last 30 days