Clinical Trials Logo

Bacteremia clinical trials

View clinical trials related to Bacteremia.

Filter by:

NCT ID: NCT00614679 Completed - Clinical trials for End-Stage Renal Disease

A Novel Catheter Lock Solution for Treatment of Tunneled Hemodialysis Catheter-Associated Bacteremia

Start date: October 2006
Phase: Phase 1
Study type: Interventional

The primary objective is to investigate the ability of systemic intravenous antibiotic plus antibiotic/anti-biofilm (i.e. N-acetylcysteine) lock catheter technique in eradicating uncomplicated catheter associated bacteremia and salvaging the infected vascular catheter. Secondary objectives include duration to clearance of bacteremia, future recurrence of bacteremia, need for catheter removal and death.

NCT ID: NCT00609375 Completed - Sepsis Clinical Trials

Efficacy of Cefepime Continuous Infusion Versus an Intermittent Dosing Regimen

CEFPK/PD
Start date: September 2006
Phase: Phase 4
Study type: Interventional

To determine the efficacy of the administration of 7 to 14 days of cefepime in a continuous infusion vs an intermittent (every 8 hours) administration, in adult patients hospitalized in Bogotá with sepsis and bacteremia caused by gram negative bacilli. The outcome was the rate of clinical cure and microbiological cure after 7 and 14 days of initiation of therapy and rates of relapse after 28 days. Hypothesis: The administration of beta lactams in continuous infusion allows a clinical or microbiological cure greater than the intermittent administration.

NCT ID: NCT00571259 Completed - Bacteremia Clinical Trials

Prophylactic Antimicrobial Catheter Lock

ALLOCK
Start date: September 2003
Phase: Phase 4
Study type: Interventional

This is a randomized, double blinded, prospective, multicenter, clinical trial of the use of Heparin versus Gentamicin as a pos-dialysis catheter lock solution.

NCT ID: NCT00555282 Completed - Clinical trials for Catheter Related Bloodstream Infection

Rate of Catheter Colonization and Risk of Bloodstream Infection During Use of Two Different Central Venous Catheters (CVC)

Start date: November 2005
Phase: Phase 4
Study type: Interventional

The use of these catheters is associated with infectious complications that are an important iatrogenic source of morbidity and mortality. Certofix® protect is a catheter with a surface modified in order to reduce colonization by bacteria. This clinical trial is performed to compare the safety and efficacy of the coated central venous catheter, Certofix® protect, with that of the non-coated standard catheter Certofix®.

NCT ID: NCT00548002 Completed - Sepsis Clinical Trials

Combination Therapy With Fluoroquinolone in Staphylococcus Aureus Bacteremia

FINLEVO
Start date: January 1999
Phase: Phase 4
Study type: Observational

To study whether fluoroquinolone (trovafloxacin or levofloxacin), added to standard treatment, could reduce the high mortality and complication rates in Staphylococcus aureus bacteremia.

NCT ID: NCT00515151 Completed - Clinical trials for Bacterial Infections

Prevention of Catheter-Associated Infection With the Skin Disinfectant Octenidine Dihydrochloride

Start date: May 2002
Phase: Phase 4
Study type: Interventional

Health-care-acquired infections are of tremendous importance for patients, especially catheter-associated infections. More than 40% of all bloodstream infections are associated with central venous catheters (CVC; catheters which are inserted into a large vein near the heart). Of all patients that acquire such an infection 1% to 5% die as a result from it. The insertion site is the main source of contamination and infection. In general, bacteria of the skin are the cause of infection, especially in short-term CVCs (10-14 days). Therefore it is necessary to efficiently disinfect the skin for the preparation and care of CVC insertion sites. Several substances are used for disinfection. Alcohol-based disinfectants are mainly used in Central Europe, other preparations contain povidine-iodine or chlorhexidine. Alcoholic disinfectants have a rapid initial effect, chlorhexidine shows an additional remanent (longer lasting) effect. A further substance, octenidine dihydrochloride, also demonstrated a remanent effect in a pilot study with neurosurgical patients. The purpose of our study is to compare an alcohol-based disinfectant containing octenidine dihydrochloride with a pure alcoholic disinfectant regarding efficacy and tolerability in patients receiving a CVC for a minimum of 5 days.

NCT ID: NCT00454285 Completed - Bacteremia Clinical Trials

Bacteria Entering the Blood Stream From Tooth Extractions and Tooth Brushing

Start date: January 2003
Phase: Phase 2
Study type: Interventional

The major purposes of this prospective, randomized, clinical study are to: 1. Determine and compare the true incidence, nature, magnitude, and duration (INMD) of bacteremia (bacteria found in the bloodstream) resulting from a highly invasive dental office procedure (tooth extraction) and a minimally invasive and naturally occurring source of bacteremia (tooth brushing); 2. Measure the effect of the American Heart Association's guidelines for amoxicillin prophylaxis (preventive treatment) on the INMD of bacteremia resulting from a single tooth extraction.

NCT ID: NCT00448942 Completed - MRSA Colonization Clinical Trials

The Impact of Chlorhexidine-Based Bathing on Nosocomial Infections

Start date: November 2004
Phase: N/A
Study type: Observational

The purpose of this study was to determine if the use of daily chlorhexidine bathing would decrease the incidence of MRSA and VRE colonization and healthcare associated Bloodstream Infections (BSI) among Intensive Care Unit (ICU) patients.

NCT ID: NCT00417235 Completed - Bacteremia Clinical Trials

Dressing: Frequency of Change and Evaluation of an Antiseptic-Impregnated Catheter Dressing in ICU Patients

DRESSING
Start date: January 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether a catheter dressing every 7th day is not inferior to a catheter dressing every 3 days and if Chlorhexidine impregnated sponges are effective in preventing catheter-related infections in ICUs.

NCT ID: NCT00414362 Completed - Bacteremia Clinical Trials

Clinical Impact of Fluoroquinolone Resistance in Bacteremia Caused by Gram-Negative Bacilli of Urinary Tract Origin

Start date: February 2007
Phase:
Study type: Observational

The information collected will optimize the management of patients with urinary tract infections with secondary bacteremia, primarily with gram negative bacteria especially Escherichia coli. The current IDSA guideline endorses the use of fluoroquinolones and trimethoprim-sulfamethoxazole as the first line agents. However, over use of this empiric regimen could result in in appropriate treatment of bacteremia.