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Infection clinical trials

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NCT ID: NCT00323453 Completed - Appendicitis Clinical Trials

Wound Infection Alexis Wound Retractor

Start date: March 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the incidence of surgical site wound infection will be reduced in open appendectomy patients through the use of the Alexis® wound retractor.

NCT ID: NCT00321165 Completed - Sepsis Clinical Trials

The AOT (Acridine Orange and Taurolidine) Trial

Start date: June 2006
Phase: Phase 3
Study type: Interventional

Total parenteral (intravenous) nutrition in the home setting (Home TPN or HPN) is a life saving strategy in patients who suffer from severe intestinal failure. Unfortunately, this treatment modality remains complicated by the development of frequent infectious complications. This especially relates to the device that is used to establish venous access, mostly a catheter (Hickman-Broviac type) or a port-a-cath. Taurolodine is an antimicrobial agent without any known side effects or resistance-related problems that holds promise as an effective antibiotic lock solution to prevent catheter infections, as demonstrated recently in a pilot study in HPN patients [Jurewitsch, 2005]. In addition, recently a test has been described which may enable to confirm a suspected diagnosis of central line infection within one hour, the so-called Acridine Orange Leukocyte Cytospin test (AOLC) [Bong, 2003]. For this test, blood that is drawn from the central line is stained with the fluorescent dye acridine orange. Next, microscopic evaluation for the presence of micro-organisms takes place. Implementation of this test might enable to start treatment of the infection and prevent unnecessary removal of non-infected central lines without the necessity to several days wait for culture results.

NCT ID: NCT00318591 Completed - Clinical trials for Urinary Tract Infections

Comparative Study of Intermittent Catheters and Occurrence of Urinary Tract Infections

Start date: April 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the frequency of urinary tract infections with symptoms in spinal cord injured patients requiring intermittent catheterization for emptying the bladder. Patients will use either a coated catheter or an uncoated catheter with gel.

NCT ID: NCT00316043 Completed - Clinical trials for Urinary Tract Infections

Prevention of Renal Failure in Children With Urinary Tract Infections

Start date: May 2006
Phase: N/A
Study type: Interventional

The aim of the study is to describe the current clinical management of young children with urinary tract infections in Dutch primary care and also to describe the possibilities for improvement and potential cost-efficiency of improved care in the light of preventing renal failure.

NCT ID: NCT00312468 Completed - HIV Infections Clinical Trials

Examining the Link Between Heart Disease and HIV Infection in Women

Start date: October 2006
Phase:
Study type: Observational

Recent studies have shown that HIV infected individuals have an increased risk of developing heart disease, but the reason for this is not fully understood. This study will examine ultrasound test results of blood vessels and laboratory data of HIV infected and HIV uninfected women to examine the link between heart disease and HIV infection.

NCT ID: NCT00309114 Completed - Clinical trials for Urinary Tract Infections

Prevention of Urinary Tract Infection (UTI) in Persons With Spinal Cord Injury (SCI)

Start date: February 2004
Phase: N/A
Study type: Interventional

Urinary tract infection (UTI) is the most common infection in patients with spinal cord injury (SCI) and is linked to major undesired results or complications including death. The bladder of SCI patients, especially those with indwelling catheters, is usually colonized by bacteria, some of which do and others which do not cause symptoms of UTI. Bacteria that do not cause symptoms are often called benign colonizers and are often left untreated because they may provide some protection against infection with more harmful bacteria. This idea of using benign bacteria to prevent infections with symptoms is called bacterial interference. A prototype strain, Escherichia coli 83972, was shown to begin and continue for extended periods of time non symptom causing colonization of the human bladder and to hold back symptom causing infections of the neurogenic bladder. Data from pilot studies at two medical centers indicated that bacterial interference might be a useful therapy for reducing the rate or frequency of UTI in SCI patients. Because almost all SCI patients have a UTI at some time, and also the large costs of treating this infection, studying the impact of bladder colonization with E. coli 83972 on the rate of symptom causing UTI has an amazing potential for improving the quality of life of SCI patients and decreasing the cost of health care. Like with other preventive plans such as vaccination, for instance, it is important to explore the effectiveness of this new preventive approach. The project is a prospective, randomized, double blind, multi-center study that deals with specific pieces of bacterial interference in SCI patients. HYPOTHESES: Placing non symptom causing bacteria (E. coli 83972) into SCI patients' bladders reduces the rate of symptom causing UTI. A. SPECIFIC AIM: Determine how bladder colonization with E. coli 83972 or similar bacteria affects the rate of symptom causing urinary tract infections in a large group of SCI and Spina Bifida patients by conducting a prospective, randomized, placebo-controlled, multi-center clinical trial.

NCT ID: NCT00308906 Completed - Infection Clinical Trials

Identification of Gene and Protein Markers of Kidney Injury in Aminoglycoside-treated Children

Start date: June 2006
Phase: N/A
Study type: Observational

The purposes of this study are to identify potential gene and protein markers of aminoglycoside-induced kidney injury in infants, children and adolescents treated with aminoglycoside antibiotics.

NCT ID: NCT00304382 Completed - Pneumonia Clinical Trials

Humoral Determinants of Immunity to Pneumococcal Infection

Start date: January 1, 2003
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether there are differences in the level of antibody to capsular polysaccharides of S. pneumoniae or the physiological activity of such antibody after vaccinating patients who have recovered from pneumococcal pneumonia with pneumococcal polysaccharide vaccine (Pneumovax) or conjugate pneumococcal vaccine (Prevnar).

NCT ID: NCT00303589 Completed - Clinical trials for Soft Tissue Infections

A Study of Beta-Lactam in Hospitalized Patients With Skin and Skin Structure Infections

Start date: December 2005
Phase: Phase 2
Study type: Interventional

This 3 arm study will compare the efficacy and safety of beta-lactam with that of 'standard care' in patients with complicated skin and skin structure infections requiring hospitalization. Patients will be randomized to receive 1)beta-lactam 750mg iv q8h 2)beta-lactam 1500mg iv q8h or 3)'standard care' [PRP (nafcillin or flucloxacillin) or vancomycin, plus aztreonam or ciprofloxacin]. The anticipated time on study treatment is <3 months and the target sample size is 100-500 individuals.

NCT ID: NCT00302640 Completed - Rotavirus Infection Clinical Trials

Study of Nitazoxanide Suspension in the Treatment of Diarrhea Caused by Enteric Viruses in Children

Start date: February 2005
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine the effect of nitazoxanide suspension in treating diarrhea caused by enteric viruses in children less than 12 years of age.