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About
General objective
This pilot study aims to compare the prevalence of resistance in bacteria causing UTIs among patients seeking care outside the hospital settings (CDROs) to the WHO-GLASS data.
Specific objectives
2-1 Primary objectives:
2-2 Secondary objectives:
Enrollment
Sex
Volunteers
Inclusion criteria
acute (< 2 weeks) dysuria. increased urinary urgency and frequency, irritation, discharge. increased lower abdominal pain or discomfort and sometimes gross haematuria.
Exclusion criteria
3,000 participants in 2 patient groups
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Central trial contact
Catrin E Moore, DPhil, MBA, MSc, BSc, FRSB, FI; Henry Kajumbula, PhD
Data sourced from clinicaltrials.gov
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