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Urinary Tract Infections clinical trials

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NCT ID: NCT00787085 Completed - Clinical trials for Urinary Tract Infections

The Significance of Funguria in Hospitalized Patients

FACES
Start date: September 2001
Phase: N/A
Study type: Observational

This investigation is a epidemiologic case-control study of the risk factors associated with nosocomial funguria (fungi in the urine).

NCT ID: NCT00781625 Recruiting - Clinical trials for Urinary Tract Infections

Probiotics as a Prophylactic Aid in Women With Recurrent Urinary Tract Infections (UTI's)

Start date: October 2008
Phase: N/A
Study type: Interventional

To investigate if administration of probiotics, either orally or vaginally, - Can reduce the number of episodes of acute bacterial cystitis and/or - Has tolerable adverse effect profile - Improves general QoL in these women - Improves the immune function and other physiological stress markers - Reduces inflammation in urinary bladder epithelium

NCT ID: NCT00771316 Terminated - Clinical trials for Urinary Tract Infections

Clinical Trial to Study the Safety and Effectiveness of MK0826 and Other Antibiotic Therapy in Patients With Complicated Urinary Tract Infection (0826-054)

Start date: December 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to demonstrate that MK0826 is comparable to Meropenem in the treatment of complicated Urinary Tract Infections (UTIs) in adults.

NCT ID: NCT00767988 Withdrawn - Clinical trials for Urinary Tract Infection

Probiotics in Girls With Spina Bifida

Start date: n/a
Phase: Phase 2
Study type: Interventional

Girls with spina bifida also have bladder problems. This is because they need temporary placement of a tube into the bladder to remove urine. This thin flexible tube is called a catheter. It can increase the risk of having bacteria in the urine. This in turn can lead to urinary tract infection (UTI). Some girls with spina bifida are given antibiotics. These are medicines used to treat infections caused by bacteria. The medicine is used to prevent UTI. However, long-term treatment with these medicines can have side effects. For example, the bacteria may become resistant to the antibiotics. Also, bacteria in the urine can persist. UTI can still occur in patients on antibiotics. UTI in girls occurs because bacteria migrate from the rectum to the vagina area. This gives the bacteria access to the bladder. Also, in girls with spina bifida, the access to the bladder is easier because of the catheter. Probiotics are friendly bacteria. They are available as dietary supplements and as food. They contain helpful bacteria. Yogurt is an example of a food that contains probiotics. The purpose of this study is to find out, if probiotics taken for 6 months can prevent UTI in girls with spina bifida. We will also try to find out whether changes in urine bacteria are associated with the taking of the probiotics. A vaginal and rectal swab will also be done to find out if taking probiotics has any benefits on preventing bacteria.

NCT ID: NCT00734968 Completed - Clinical trials for Post-Operative Urinary Tract Infection in Patients Undergoing Placement of a Sub-Urethral Sling for the Treatment of Stress Urinary Incontinence

Does Post-Operative Prophylaxis With Macrobid Reduce the Incidence of Post-Operative Urinary Tract Infection in Patients Undergoing Placement of a Sub-Urethral Sling for the Treatment of Stress Urinary Incontinence

Start date: May 2008
Phase: Phase 4
Study type: Interventional

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.

NCT ID: NCT00732238 Completed - Spinal Cord Injury Clinical Trials

Multifaceted Treatment of Catheter-related Urinary Tract Infection

Start date: July 2007
Phase: Phase 2
Study type: Interventional

The specific objective of this clinical trial is to demonstrate that a multifaceted approach for treatment for catheter-related urinary tract infection (UTI) in patients with spinal cord injury is effective and feasible. We plan to test the following hypothesis: a multifaceted treatment approach that consists of immediate removal of the indwelling bladder catheter, selecting antibiotics based on the finding from a urine culture that is obtained through the newly inserted catheter, and a 5-day course of systemic antibiotics will effectively treat catheter-related infection that is limited to the lower urinary tract of patients with spinal cord injury.

NCT ID: NCT00731315 Terminated - Clinical trials for Urinary Tract Infections

Computer-Assisted Treatment of Urinary Tract Infection in Emergency Departments and Community Health Centers

UTI-Kiosk
Start date: August 2008
Phase: N/A
Study type: Interventional

Our study aims to test the utility of computer-assisted treatment for uncomplicated, recurrent urinary tract infections (UTIs) for women receiving care in safety net health care facilities. As of November 2009, we are also testing the utility of computer-assisted treatment for certain types of complicated cystitis (i.e. women with voiding symptoms and one of the following complicating symptoms: fever, flank pain, or symptoms greater than 7 days).

NCT ID: NCT00722735 Completed - Clinical trials for Urinary Tract Infections

Finafloxacin 300 mg Twice a Day (b.i.d.) Versus Ciprofloxacin 250 mg Twice a Day (b.i.d) in Patients With Lower Uncomplicated UTI (uUTI)

FLUT
Start date: October 2008
Phase: Phase 2
Study type: Interventional

To compare the bacteriological eradication rates of Finafloxacin and Ciprofloxacin in female patients with uUTI.

NCT ID: NCT00714792 Completed - Overactive Bladder Clinical Trials

Pilot Study: Is Overactive Bladder Caused by Subacute Urinary Tract Infections?

Start date: June 2008
Phase: N/A
Study type: Observational

The purpose of this study is to look for evidence of bacteria in the urine or bladder of people with overactive bladder. Because you do not have overactive bladder, your participation in this study will be used as a comparison to those who have overactive bladder.

NCT ID: NCT00714402 Completed - Clinical trials for Bacterial Infections

Procalcitonin Level and Kinetics in Children With Bacterial Infections

Start date: August 2008
Phase: N/A
Study type: Observational

The purposes of this study are: 1. To determine whether procalcitonin level at admission of pediatric patients with bacterial infections can be used as a marker for prediction of defervescence and hospitalization length 2. To examine the kinetics of procalcitonin in pediatric patients with bacterial infections and persistent fever