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Wound Infection clinical trials

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NCT ID: NCT04917627 Recruiting - Wound Infection Clinical Trials

To Assess Use of Vancomycin Powder in Craniotomy on Wound Infection Rates

Start date: May 1, 2021
Phase: Phase 4
Study type: Interventional

Surgical site infection (SSI) after craniotomy is a major cause of morbidity and mortality besides its major health care cost. In each hospital, all measures are taken to decrease SSI. Despite current prophylactic measures, rates of SSIs have been reported in up to 5% of patients post craniotomy. Intrawound vancomycin powder has been studied extensively in spinal fusion surgeries and been found to reduce rates of surgical site infections (SSIs) significantly. Despite its success in spinal surgeries, topical vancomycin has not been extensively studied with respect to cranial neurosurgery. The use of adjuvant vancomycin powder was associated with a significant reduction in the incidence of postoperative infection as well as infection-related medical costs. These findings suggest that the use of adjuvant vancomycin powder in high-risk patients undergoing spinal fusion is a cost-saving option for preventing postoperative infections, as it can lead to cost-savings of $438,165 per 100 spinal fusions performed. The investigators believe that Topical vancomycin is a safe, effective, and cost-saving measure to prevent SSIs following craniotomy.

NCT ID: NCT04906642 Terminated - Clinical trials for Surgical Wound Infection

Clinical Assessment of Next Science Solution on Gustilo and Anderson Type II and IIIA or IIIB Tibial Fractures

Start date: May 4, 2021
Phase: N/A
Study type: Interventional

This is a prospective, randomized, controlled, double-blinded clinical feasibility study of subjects that are being treated for Gustilo and Anderson Type II or IIIA or IIIB Tibial Fractures

NCT ID: NCT04900298 Recruiting - Clinical trials for Surgical Wound Infection

Reducing Intraoperative ESKAPE Transmission Through Use of a Personal Hand Hygiene System

ESKAPE
Start date: January 1, 2022
Phase: N/A
Study type: Interventional

The investigators hypothesize that the use of a personal hand hygiene system (SafeHavenTM) by anesthesia providers in the adult operating room, combined with a novel infectious pathogen tracking system (OR PathTrac) will decrease participant exposure to pathologic bacteria in the adult operating room.

NCT ID: NCT04840576 Recruiting - Clinical trials for Surgical Wound Infection

Prophylactic Negative Wound Pressure Therapy (PICO-7) Following Groin Incisions in Vascular Surgery (PICO-Vasc Study)

PICO-Vasc
Start date: April 15, 2021
Phase: N/A
Study type: Interventional

Comparison between waterproof sterile dressing OPSITE Post-Op Visible, Smith & Nephew, UK and PICO-7, Smith & Nephew, UK in terms of inguinal surgical wound infection and complications after lower limb revascularization.

NCT ID: NCT04831112 Completed - Wound Infection Clinical Trials

Compare Effects of Dressing With Honey and EUSOL

Start date: March 1, 2020
Phase: N/A
Study type: Interventional

Honey is super saturated solution containing sugar derived from nectar gathered by honeybee. Honey is viscus supersaturated solution mainly composed of sugar and water along with minor constituents such as minerals, vitamins, amino acids, organic acids, flavonoids, and other phenolic compound and aromatic substances. Honey contents according to percentages are fructose 38.6%, glucose 31%, water 17%, lactose 7.2%, larger sugars 4.7% and rest of micronutrients and elemental compounds are 1.5%. Honey enhances wound healing by removing slough and necrotic tissue from wound. It promotes wound healing by increasing angiogenesis, granulation and epithelization. Honey possess antimicrobial activity against bacteria like methicillin resistant staphylococcus aureus, vancomycin resistant Escherichia Coli, pseudomonas aeruginosa, and many other species. It also has activity against some yeast species such as aspergillus and penicillium. Honey used for dressing will be 'Langnese Honey". Langnese honey is raw honey / unprocessed packed as collected, quality and quantity will be same for patients.

NCT ID: NCT04788381 Not yet recruiting - Colorectal Cancer Clinical Trials

The Effects of Preoperative Bevacizumab on Perioperative Complications

Start date: April 1, 2021
Phase:
Study type: Observational

This is a nationwide multicenter,retrospective,observational real-world study. 1. To assess the risk of perioperative complications in patients with tumor who received bevacizumab prior to unexpected operation. 2. To assess the correlation of the interval time between the last dose of bevacizumab and operation and occurrence of perioperative complications. 3. To explore the risk factors of perioperative comlications in patients with tumor received bevacizumab prior to unexpected operation.

NCT ID: NCT04785404 Completed - Wound Infection Clinical Trials

Primary Versus Secondary Closure of Stoma-Reversal Skin Wound

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

to compare infection rate stoma reversal skin wound after primary or secondary closure

NCT ID: NCT04725916 Recruiting - Clinical trials for Postoperative Complications

Studying How Outpatient Water affEcts Risks With Drains (SHOWER Study)

SHOWER
Start date: February 23, 2022
Phase: N/A
Study type: Interventional

This is a prospective randomized, controlled, unblinded, interventional feasibility study to evaluate if showering with post operative drains in place leads to an increase in complications. The patients included in the study will be those undergoing breast reductions and panniculectomies at Geisinger Medical Center. The patients will be randomized post operatively into one of two groups: 1) patients instructed to shower with drains in place, and 2) patients instructed not to shower while they have drains in place.

NCT ID: NCT04618276 Completed - Clinical trials for Surgical Site Infection

Effect of Photodynamic Therapy on Skin Microbiome. Single Center Study (PHOMIC-II)

Start date: January 15, 2021
Phase: N/A
Study type: Interventional

The overarching aim of this research project is to prevent orthopedic implant-associated infections. This study aims to investigate if PDT has an effect on bacterial skin colonization in order to improve skin antisepsis strategies for the prevention of surgical site infections.

NCT ID: NCT04609384 Recruiting - Clinical trials for Bacterial Infections

Nudging Effect of Timer on Surgical Rub

Start date: January 1, 2020
Phase:
Study type: Observational

To study whether a device has a nudging effect on the time spend on surgical rub.