Noroxin Efficacy and Safety Trial (NEST)
Urinary Tract Infections
About this trial
This is an interventional treatment trial for Urinary Tract Infections focused on measuring urinary tract infection, Norfloxacin, Fluroquinolone, Safety, Pakistan
Eligibility Criteria
Inclusion Criteria:
- Written informed consent
- At least one typical symptom of acute, lower urinary tract infection out of dysuria, frequency, macrohaematuria, cloudy or smelly urine or self-diagnosed cystitis
Exclusion Criteria:
- Duration of UTI symptoms for more than 7 days before physician's visit
- Clinical signs of invasiveness such as fever (axillary body temperature >38 degrees Celsius), costovertebral pain or tenderness, rigors, nausea or vomiting
- Known or suspicion of anatomical or functional abnormality of the urinary tract
- Vaginal symptoms: discharge, irritation
- Diabetes mellitus
- Immunosuppression (e.g. prednisone equivalent >10mg per day for >14 days, chemotherapy, radiotherapy, immunomodulators, HIV infection, neutropenia)
- Any other serious comorbidity as judged by the treating physician
- Bladder catheter in situ or during the past 30 days
- Pregnancy
- Recurrent urinary tract infection (more than 3 infections during the last 12 months)
- Antibiotic treatment during the last 4 weeks
Sites / Locations
Arms of the Study
Arm 1
Experimental
Norofloxacin
The recommended dosage of norfloxacin for urinary-tract infections in adults is 400 mg orally every 12 hours; the drug should be given for 7 to 10 days in uncomplicated infections and for 10 to 21 days in complicated ones. Adverse drug effects were mild and included disturbances of the gastrointestinal tract and the central nervous system. The study shall be completed in accordance with the ICH topic E6 (R1)(CPMP/ICH/one hundred thirty five/95) guiding principle for top medical practice and the ideas enunciated within the announcement of Helsinki and the approval by way of an Institutional Ethics Committee.