Expired Study
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Temple, Texas 76508


Purpose:

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 incidence of postoperative urinary tract infection in women receiving sub-urethral slings for the treatment of urinary incontinence.


Criteria:

Inclusion Criteria: - Women over the age of 18 who will undergo the placement of a sub-urethral sling for the treatment of stress urinary incontinence Exclusion Criteria: - 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).


NCT ID:

NCT00734968


Primary Contact:

Principal Investigator
Daniel L Jackson, M.D.
University of Missouri-Columbia


Backup Contact:

N/A


Location Contact:

Temple, Texas 76508
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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