Does Treatment With Macrobid Reduce Urinary Tract Infections in Patients Receiving a Sub-Urethral Sling for Incontinence
Completed · Phase 4 · Has a placebo group
Conditions studied: Stress Incontinence
In brief
This project will determine whether post-operative prophylaxis with macrobid will decrease the incidence of postoperative urinary tract infection in women receiving sub-urethral slings for the treatment of urinary incontinence.
Key facts
- Study ID
- NCT00734968
- Run by
- University of Missouri-Columbia
- People needed
- 161
- Starts
- 2008-05-01
- Expected to finish
- 2010-05-01
- Last updated by the study team
- 2016-10-11
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Women over the age of 18 who will undergo the placement of a sub-urethral sling for the treatment of stress urinary incontinence
You may not qualify if…
- Exclusion criteria are those with a known allergy to macrobid, those with glucose-6-phosphate deficiency, renal impairment, women breast feeding or with a known pregnancy, patients taking medications for gout, and those with known risk factors for complicated UTI (polycystic renal disease, nephrolithiasis, neurogenic bladder, diabetes, immuno-suppression, etc).
Where it is running
- Scott and White Hosptial, Texas A&M University — Temple, Texas, United States
Full record on ClinicalTrials.gov
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