Status:
COMPLETED
Does Treatment With Macrobid Reduce Urinary Tract Infections in Patients Receiving a Sub-Urethral Sling for Incontinence
Lead Sponsor:
University of Missouri-Columbia
Collaborating Sponsors:
Texas A&M University
Conditions:
Stress Incontinence
Eligibility:
FEMALE
18+ years
Phase:
PHASE4
Brief Summary
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 treatme...
Detailed Description
This project will be a randomized, double blinded, placebo controlled clinical trial. The aim of the trial is to determine whether or not post-operative prophylaxis with macrobid will decrease the inc...
Eligibility Criteria
Inclusion
- Women over the age of 18 who will undergo the placement of a sub-urethral sling for the treatment of stress urinary incontinence
Exclusion
- 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).
Key Trial Info
Start Date :
May 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2010
Estimated Enrollment :
161 Patients enrolled
Trial Details
Trial ID
NCT00734968
Start Date
May 1 2008
End Date
May 1 2010
Last Update
October 11 2016
Active Locations (1)
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1
Scott and White Hosptial, Texas A&M University
Temple, Texas, United States, 76508