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Wound Infection clinical trials

View clinical trials related to Wound Infection.

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NCT ID: NCT01316588 Completed - Clinical trials for Surgical Wound Infection

Recolonization Following Preoperative Disinfection Plastic Adhesive Drapes

Start date: August 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to measure the time to recolonization intraoperatively after preoperative disinfection with chlorhexidine solution in ethanol and to determine evidence of differential bacterial growth with or without plastic adhesive drape on the chest as well as with or without microbial sealant on the leg.

NCT ID: NCT01292343 Completed - Wound Infection Clinical Trials

Triclosan Toothpaste and Third Molar Surgery

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

Triclosan containing dentifrices are effective in the prevention of inflammatory complications following third molar surgery through reducing preoperative oral bacteria load.

NCT ID: NCT01287780 Completed - Clinical trials for Surgical Wound Infection

Local Gentamicin Application to Reduce Postoperative Infection Rate

Start date: January 2011
Phase: Phase 3
Study type: Interventional

The majority of elderly patients with a displaced fracture of the proximal femur are now treated with a hemiarthroplasty. Prosthetic joint infection is a devastating complication, and the infection rate is high in this group of elderly patients. Local application of gentamicin produces high antibiotic concentrations in the wound. The aim of this study is to determine whether locally administered collagen-gentamicin in the joint perioperatively in addition to routine IV prophylaxis with beta-lactam antibiotics can reduce the early postoperative infection rate (< 4 weeks postoperative)after hemiarthroplasty in proximal femoral fractures.

NCT ID: NCT01252732 Completed - Wound Infection Clinical Trials

Oritavancin Versus IV Vancomycin for the Treatment of Patients With Acute Bacterial Skin and Skin Structure Infection

SOLO II
Start date: December 2010
Phase: Phase 3
Study type: Interventional

The purpose of this Phase 3 trial is to evaluate the efficacy, safety, and tolerability of oritavancin in ABSSSIs, including those caused by MRSA and to evaluate the potential economic benefit of oritavancin administered as a single 1200 mg IV dose.

NCT ID: NCT01252719 Completed - Wound Infection Clinical Trials

Oritavancin Versus IV Vancomycin for the Treatment of Participants With Acute Bacterial Skin and Skin Structure Infection (SOLO I)

SOLO I
Start date: December 2010
Phase: Phase 3
Study type: Interventional

The purpose of this Phase 3 trial was to evaluate the efficacy, safety, and tolerability of oritavancin in acute bacterial skin and skin structure infections (ABSSSIs), including those caused by methicillin-resistant staphylococcus aureus (MRSA), and to evaluate the potential economic benefit of oritavancin administered as a single 1200-milligram (mg) intravenous (IV) dose.

NCT ID: NCT01238276 No longer available - Diabetic Foot Ulcer Clinical Trials

Direct Antibiotic Delivery of Cefazolin Into Soft Tissue Infections Using Subcutaneous Injection and Ultrasonic Dispersion

DAD
Start date: n/a
Phase:
Study type: Expanded Access

This study focuses on a new drug delivery system (Direct Antibiotic Delivery) to treat soft tissue infections. In this study, cefazolin is delivered directly to the target tissues using subcutaneous injection of antibiotic solution and then dispersed using high-frequency external ultrasound. Using this system, a much higher concentration of antibiotic can be achieved than through traditional treatment methods. Unlike traditional delivery methods, Direct Antibiotic Delivery does not rely on blood supply and is beneficial for subjects with Diabetes or subjects who have received radiation therapy and blood supply is limited.

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: NCT01235546 Completed - Clinical trials for Surgical Site Infection

Study of Effectiveness and Safety of Azithromycin-based Extended-spectrum Prophylaxis to Prevent Post Cesarean Infection

C/SOAP
Start date: May 2011
Phase: N/A
Study type: Interventional

The Cesarean Section Optimal Antibiotic Prophylaxis (C/SOAP) study is a large pragmatic multi-center randomized clinical trial designed to evaluate the comparative effectiveness and safety of azithromycin-based extended-spectrum antibiotic prophylaxis (azithromycin plus standard narrow-spectrum cephalosporin) relative to standard single-agent cephalosporin (preferably prior to surgical incision) to prevent post-cesarean infection. Hypothesis: Compared to narrow-spectrum prophylaxis (i.e. cefazolin alone, or clindamycin if cephalosporin allergy) prior to surgical incision, the addition of extended-spectrum prophylaxis (azithromycin + cefazolin) reduces the incidence of post-cesarean infection.

NCT ID: NCT01220700 Completed - Wound Infections Clinical Trials

Antimicrobial Coated Sutures in Paediatric Surgery

Start date: September 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if suture material coated by antimicrobial agent triclosan would decrease the incidence of surgical site infections (SSIs) in paediatric surgery compared to ordinary sutures. 1500 children (age form 4 weeks to 18 years) coming for general pediatric surgery to the Oulu University Hospital are randomised to have sutures coated with triclosan (Vicryl Plus, Monocryl Plus) or ordinary sutures. The occurrence of SSIs is monitored by email questionnaires to the parents on days 10 and 30. The diagnosis of SSIs are made along CDC criteria.

NCT ID: NCT01212315 Completed - Clinical trials for Postoperative Wound Infection

Effects of Triclosan-coated Sutures in Cardiac Surgery

Start date: March 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess if triclosan-coated sutures reduces wound infections after saphenous vein harvesting in CABG patients. Secondary objectives are the effect triclosan-coated sutures on sternal wound infections and a cost analysis.