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Wound Infection clinical trials

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NCT ID: NCT02459093 Completed - Clinical trials for Surgical Wound Infection

Subcuticular Suture for Cesarean Skin Incision Closure

Start date: May 2015
Phase: Phase 4
Study type: Interventional

A comparison of the type of suture used for cesarean skin incision approximation and the subsequent rate of wound complications has not been widely studied. Investigators seek to compare poliglecaprone 25 and polyglactin 910 suture used in a subcuticular skin closure in Pfannenstiel incisions during cesarean birth and determine the subsequent wound complication rates (SSI, hematoma, seroma, wound separation).

NCT ID: NCT02448511 Completed - Wound Infection Clinical Trials

Local Application of Ozone Gas for Infected Ulcers

Start date: August 2013
Phase: N/A
Study type: Interventional

This study evaluates the efficacy of local application of ozone gas in healing of infected ulcers. Half the participants received conventional treatment with placebo generator and the other half received conventional treatment with ozone generator.

NCT ID: NCT02444598 Completed - Wound Infection Clinical Trials

Trial of Negative-pressure Wound Therapy Use in Conflict-related Extremity Wounds

VACoCREW
Start date: June 2015
Phase: N/A
Study type: Interventional

There is a treatment method called negative-pressure wound therapy (NPWT) that is well established and used for the treatment of wounds. The method involves the application of a wound dressing through which a negative pressure is applied. Due to a plastic film overlaying the wound the risk of wound contamination is reduced. NPWT is considered to promote wound healing and prevent infection and has previously been used in the treatment of acute war associated wounds with satisfactory results. The aim of this study is to compare NPWT with conventional wound dressings in the treatment of war-associated extremity wounds and evaluate which method is more effective.

NCT ID: NCT02400112 Terminated - Clinical trials for Surgical Wound Infection

Local Application of Vancomycin Powder in Grade I-IIIA Open Fractures

Start date: March 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if local administration of vancomycin powder at the site of Grade I-IIIA open fractures at the time of surgery will be an efficacious method to lower infection rates in open fracture treatment and to elucidate any detrimental effects of applying vancomycin powder at the site of open fractures.

NCT ID: NCT02399878 Active, not recruiting - Pneumonia Clinical Trials

Intra-operative Inspiratory Oxygen Fraction and Postoperative Respiratory Complications

Start date: January 2007
Phase: N/A
Study type: Observational

Respiratory complications represent the second most frequent type of postoperative complications with an incidence estimated to range from 2.0% to 7.9% It has been shown that intra-operative protective ventilation is associated with a reduced risk of respiratory complications. The effects of intra-operative inspiratory oxygen fraction (FiO2) remain to be investigated. In this study, the investigators aim to investigate the association between intra-operative FiO2 and respiratory complication as well as surgical site infection and ICU admission in patients undergoing non-cardiothoracic surgery. The investigators primary hypothesis is that high intra-operative FiO2 increases the risk of postoperative respiratory complications independent of predefined risk factors.

NCT ID: NCT02395159 Completed - Infections Clinical Trials

Reduction of Groin Wound Infections After Vascular Surgery by Using an Incision Management System (IMS)

IMS
Start date: July 2015
Phase: N/A
Study type: Interventional

Comparison of the Prevena™ IMS with the standard wound management method of sterile plaster in vascular surgery patients.

NCT ID: NCT02390401 Terminated - Clinical trials for Surgical Wound Infection

Vacuum Assisted Closure for Cesarean Section

VACCS
Start date: May 2015
Phase: Phase 1
Study type: Interventional

To study if incisional vacuum-assisted closure can decrease the risk of infection in cesarean section incisions in the obese compared with standard sterile dressing.

NCT ID: NCT02375178 Completed - Clinical trials for Periodontal Diseases

Antimicrobial Activity of Two Mouthwashes

Start date: August 2014
Phase: N/A
Study type: Interventional

This is a three arm randomized trial. The aim is to evaluate the antimicrobial activity of chlorhexidine and polyhexamethylene biguanide oral antiseptics on the microorganisms of the oral cavity. A total of 30 healthy volunteers will be enrolled and randomly allocated to control group (CG, n=10), which will be instructed to rinse the mouth with 10ml of a sterile saline solution for one minute, to chlorhexidine group (ClG, n=10), which will be instructed to rinse the mouth with 10ml of an 0.12% chlorhexidine solution, for one minute, or to polyhexamethylene biguanide group (PG, n=10), which will be instructed to rinse the mouth with 10ml of an 0.07% polyhexamethylene biguanide solution, for one minute. Samples of saliva will be collected before the mouth wash and after 30, 60 and 180 minutes. Samples will be plated on manitol agar, mitis salivarius agar, EMB agar and Sabouraud agar. Samples will be processed by a blinded microbiologist.

NCT ID: NCT02374853 Terminated - INFECTION Clinical Trials

Topical Use of Vancomycin in Reducing Sternal Wound Infection in Cardiac Surgery (SWI Trial)

SWI
Start date: March 2015
Phase: Phase 2
Study type: Interventional

The purpose of this research is to determine if using the antibiotic vancomycin as a preventative topical (on the surface of the skin) treatment during open-heart surgery will reduce the risk of developing a sternal wound infection.

NCT ID: NCT02374294 Withdrawn - Clinical trials for Complication of Surgical Procedure

TCOT Effectiveness in Preventing Wound Infections in Perineal Resections

Start date: September 2015
Phase: Phase 2
Study type: Interventional

In colorectal surgery, oxygen insufflation (which leads to higher oxygen concentration in the surgical site) has been shown to decrease infection rate. Several pressure wounds in the coccyx have been successfully treated to closure with Transdermal Continuous Oxygen Therapy (TCOT) Given the wound healing properties of TCOT, particularly in infection-prone anatomic locations such as coccyx, and the microbicidal properties of oxygen, it is expected that the infection rate in abdominoperineal (AP) resection surgery can be reduced with transdermal continuous oxygen therapy. The primary objective of this study is to compare the number of surgical site infections associated with perineal surgery within 28 days between subjects randomized to receive EPIFLO or Standard of Care