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Urinary Tract Infections clinical trials

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NCT ID: NCT00305227 Completed - Clinical trials for Urinary Tract Infection

Intravaginal LACTIN-V for Prevention of Recurrent Urinary Tract Infection

Start date: March 2006
Phase: Phase 2
Study type: Interventional

Recurrent urinary tract infections (RUTIS) continue to be a major health problem in women and are now complicated by increasing antibiotic resistance. New preventive approaches are needed. Because most women with RUTI lack the normal protective Lactobacillus (LB) in their vaginal flora, we hypothesized that restoration of LB would reduce RUTIS. In this trail, women with recent UTI are randomized to receive either LB or placebo vaginal capsules and are followed for side effects, for colonization with LB and for occurrence of RUTI over hte next four months.

NCT ID: NCT00305071 Not yet recruiting - Clinical trials for Urinary Tract Infections

Effect of Adjuvant Treatment With Compound Cranberry Extract Tablets in Acute Bacterial Cystitis.

Start date: April 2006
Phase: Phase 2
Study type: Interventional

In conventional treatment for non-complicated bacterial cystitis, 3-day oral antibiotics could achieve good cure rate. However, severe lower urinary tract symptoms were most bothersome and only could be partially relieved by NSAID, detrusor muscle relaxants, minor tranquilizer or pyridium. Some medication associated side effects were complained while receiving adjuvant medication treatment, including gastro-intestinal discomfort, dry mouth, blurred vision, lethargy, or allergic reactions. The irritative bladder symptoms from bladder inflammation had great impact on the quality of life and well tolerable adjuvant therapy would have clinical benefit to reduce the discomfort from the bladder. In the past years, cranberry juice or its extract has been proven to have protective effect on urothelium to prevent further bacterial ascending infection. The commercial cranberry extract tablets have good tolerability and showed good effect on symptoms reliving and infection protection on several clinical observation. In acute bladder infection, we could expect the bioactive components in cranberry could reduce the virulence of pathogens and assist to eradicate pathogens and to stable the urothelium. In literature review, only little works focusing on the symptoms relief in acute cystitis patients. To clarify the clinical benefit on lower urinary symptoms relieving, we attempt to conduct a randomized double-blind placebo-controlled trial to evaluate the effect of a compound cranberry extract tablet as an adjunctive modality in treating acute uncomplicated bacterial cystitis in otherwise healthy female patients.

NCT ID: NCT00280592 Completed - Multiple Sclerosis Clinical Trials

Cranberry for Prevention of Urinary Tract Infections in Multiple Sclerosis Patients

CANNEBERGE
Start date: January 2006
Phase: Phase 3
Study type: Interventional

Bladder dysfunction occurs at some time in most patients with multiple sclerosis and these patients are prone to have recurrent urinary tract infections. Cranberry has been traditionally used for the treatment and prophylaxis of urinary tract infections but there is no reliable randomized controlled trial demonstrating evidence of cranberry's utility in this disease. The aim of our study is to assess the efficacy and safety of cranberry in the prophylaxis of urinary tract infections in patients with multiple sclerosis with a prospective randomized, double-blind and placebo-controlled clinical trial.

NCT ID: NCT00261248 Completed - Clinical trials for Recurrent Urinary Tract Infections in Women

Vaccine for Recurrent Urinary Tract Infections in Women

Start date: November 1996
Phase: Phase 2
Study type: Interventional

The purpose of this study is determine whether a vaginal mucosal vaccine given to women with a history of recurrent urinary tract infections can reduce the number of infections occurring in a six-month study period, as compared to placebo treatment.

NCT ID: NCT00258102 Completed - Clinical trials for Urinary Tract Infections

A Study of the Safety and Effectiveness of Levofloxacin Compared With Lomefloxacin in the Treatment of Complicated Urinary Tract Infections

Start date: January 1993
Phase: Phase 3
Study type: Interventional

The purpose of the study is to compare the safety and effectiveness of oral levofloxacin (an antibiotic) with that of oral lomefloxacin in the treatment of complicated urinary tract infections in adults.

NCT ID: NCT00258089 Completed - Clinical trials for Urinary Tract Infections

A Study of the Safety and Effectiveness of Oral Levofloxacin Compared With Oral Ciprofloxacin in the Treatment of Complicated Urinary Tract Infections

Start date: June 1993
Phase: Phase 3
Study type: Interventional

The purpose of the study is to compare the safety and effectiveness of oral levofloxacin (an antibiotic) with that of oral ciprofloxacin in the treatment of complicated urinary tract infections in adults.

NCT ID: NCT00245791 Terminated - Clinical trials for Complicated Urinary Infection

Urinary Tract Infection Study With the Antibiotic Levofloxacin Given at a Higher Dose Over a Shorter Period of Time

Start date: October 2004
Phase: Phase 4
Study type: Interventional

The purpose of the study is to compare the safety and effectiveness of the antibiotic levofloxacin by administering a higher dose of levofloxacin and using a shorter course of therapy.

NCT ID: NCT00243360 Completed - Clinical trials for Urinary Tract Infection, Antibiotic Use

Optimizing Antibiotic Use in Long Term Care

Start date: January 2001
Phase: N/A
Study type: Interventional

The purpose of this study was to determine if a multi-faceted intervention to implement diagnostic and therapeutic algorithms for management of suspected urinary infection in nursing home residents could reduce antibiotic prescribing for urinary indications in this population.

NCT ID: NCT00229021 Completed - Clinical trials for Urinary Tract Infections

Doripenem in the Treatment of Complicated Lower Urinary Tract Infection or Pyelonephritis

Start date: December 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the microbiological cure rate of doripenem versus a comparator antibiotic in the treatment of patients with complicated urinary tract infection or pyelonephritis. The study will also characterize the safety and tolerability of treatment with doripenem in patients with complicated urinary tract infection or pyelonephritis.

NCT ID: NCT00216853 Completed - Clinical trials for Urinary Tract Infections

A Study of Vaginal MicroFlora and Immune Profiles of Patients With Recurrent Urinary Tract Infection

Start date: September 2003
Phase: N/A
Study type: Observational

The purpose of this study is to determine the extent to which vaginal microflora and immune profiles of patients with urinary tract infection (UTI) differ from healthy controls.