Clinical Trials Logo

Wound Infection clinical trials

View clinical trials related to Wound Infection.

Filter by:

NCT ID: NCT01629030 Recruiting - Clinical trials for Coronary Artery Bypass Graft

Risk Factors of Sternal Wound Infection After Coronary Artery Bypass Graft

Start date: June 2012
Phase: N/A
Study type: Observational

The investigators are trying to evaluate the performance of neutrophil and lymphocyte counts as a risk factor of deep sternal wound infection after coronary artery bypass graft surgery.

NCT ID: NCT01324804 Recruiting - Clinical trials for Coronary Heart Disease

Antibiotic Concentration in Internal Mammary Graft Preparation

Start date: November 2010
Phase: N/A
Study type: Observational

The negative effect of internal mammary harvesting on sternal perfusion is well known, especially in diabetic subjects. Microdialysis previously showed increased lactate tissue concentration after mammary artery preparation. Although high antibiotic concentration is of utmost importance in this region, no study previously measured the effect of internal mammary artery harvesting on target tissue antibiotic concentration. Study hypothesis: Internal mammary artery harvesting imposes an additional risk for deep sternal wound infection by impairing antibiotic tissue penetration. This effect is mediated by altered perfusion patterns and may be seen in cephalosporin and/or Teicoplanin treatment. Study objective: To evaluate the impact of left internal mammary artery preparation on target tissue antibiotic concentration of Cefazolin and Teicoplanin during cardiac surgery Design: This study is designed as an observational pharmacokinetic trial. Patients are their own controls by measuring antibiotic concentration in different subcutaneous tissues. Study population: Patients referred for coronary artery bypass grafting to the Department of Cardiothoracic Surgery with planned unilateral left internal mammary artery preparation and a high risk profile for deep sternal wound infections will be asked to participate in this trial.

NCT ID: NCT01237730 Recruiting - Clinical trials for Prophylactic Antibiotics Before PEG

Tailored Antibiotics Prophylaxis for Percutaneous Endoscopic Gastrostomy

PEG
Start date: July 2010
Phase: N/A
Study type: Interventional

Tailored antibiotic prophylaxis according to the individual throat swab culture could reduce the peristomal infection rate

NCT ID: NCT00150852 Recruiting - Wound Infection Clinical Trials

Prevention of Gastrostomy-Related Wound Infection by Vancomycin in Carriers of Methicillin-Resistant Staphylococcus Aureus.

Start date: September 2004
Phase: Phase 2
Study type: Interventional

The aim of this study is to determine whether vancomycin with cefazoline is superior to vancomycin with placebo in preventing gastrostomy-related wound infection in carriers of methicillin-resistant staphylococcus aureus (MRSA).