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Surgical Wound Infection clinical trials

View clinical trials related to Surgical Wound Infection.

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NCT ID: NCT04310878 Completed - Clinical trials for Surgical Site Infection

Gaps Between Evidence and Practice in Prevention of Surgical Site Infection in Spain

SurveyOIC
Start date: April 1, 2019
Phase:
Study type: Observational

Web-based survey to members of 10 Spanish Associations of surgical nurses and surgeons of different specialities to know the application of preventative measures for surgical site infection.

NCT ID: NCT04303390 Completed - Clinical trials for Surgical Site Infection

24 Vs 48 Hours of Cefazolin or Cefuroxime as Prophylaxis

Start date: February 6, 2018
Phase: Phase 4
Study type: Interventional

A randomized control trial studying the effect of prophylactic antibiotics to reduce surgical site infections following cardiac surgery in adults using 1st generation cephalosporin (Cefazolin) or 2nd generation cephalosporin (Cefuroxime).

NCT ID: NCT04299737 Withdrawn - Clinical trials for S. Aureus Transmission

Improving Case Selection for Perioperative S. Aureus Transmission Surveillance to Reduce Surgical Site Infections

Start date: March 9, 2020
Phase:
Study type: Observational

The first patient in the dyad will receive the bundle, which includes patient decolonization methods, environmental cleaning in the OR, a hand hygiene system located on the IV pole for the anesthesia provider, and intravascular catheter and syringe tip disinfection practices. The second patient in the dyad will receive usual care. Both patients will be surveyed by obtaining swab samples at the beginning and end of the surgery using the OR PathTrac kits. The OR PathTrac software (RDB Bioinformatics, Omaha, NE 68154) uses algorithms to guide analysis of the S. aureus isolates and to identify transmission events. Transmission stories are processed by the software to generate transmission maps that identify improvement successes and failures. It also identifies actionable steps to improve the bundle. The perioperative infection control team then uses this information to continually optimize the bundle, and the software to measure the effect.

NCT ID: NCT04285697 Suspended - Brain Tumor Clinical Trials

Infection Prevention Bundle in Brain Tumor Surgery

Start date: February 20, 2020
Phase: N/A
Study type: Interventional

This study aimed to evaluate the effectiveness of an infection prevention bundle on surgical site infections in patients undergone brain tumor surgery. The patients were divided into 2 groups: infection prevention bundle group and control group

NCT ID: NCT04281667 Active, not recruiting - Colorectal Cancer Clinical Trials

Mechanical Bowel Preparation and Oral Antibiotics Versus Mechanical Bowel Preparation Only Prior Rectal Surgery

MOBILE2
Start date: March 18, 2020
Phase: Phase 4
Study type: Interventional

MOBILE2 is a randomized controlled trial comparing mechanical and oral antibiotic bowel preparation to mechanical bowel preparation only in patients undergoing anterior rectal resection with primary anastomosis. Primary endpoint is Comprehensive Complication Index within 30 days from surgery.

NCT ID: NCT04280237 Withdrawn - Clinical trials for Surgical Site Infection

Pharmacological Study of Cefazolin Antibioprophylaxis in Liver Transplantation

ProCeTH
Start date: March 2020
Phase:
Study type: Observational

This study describes Cefazolin pharmacokinetics variation to target levels during liver transplantation.

NCT ID: NCT04265612 Terminated - Clinical trials for Wound Infection, Surgical

Effect of the Negative Pressure Therapy Dressing Compared With Hydrogel Dressing.

PICO/2019
Start date: November 5, 2019
Phase: N/A
Study type: Interventional

The objective of the study is to measure the efficacy of the use of single-use portable negative pressure therapy (PICO ®) in the prevention of surgical wound infections (SSI) from cardiac surgery under extracorporeal circulation compared to single-use hydrocolloid dressings "Aquacel Surgical".

NCT ID: NCT04258878 Not yet recruiting - Clinical trials for Surgical Wound Infection

Prospective Cohort Study in Evaluation of Risk Factors for Infection During and After Coronary Graft Operations.

Start date: April 1, 2020
Phase:
Study type: Observational [Patient Registry]

We aim to prospectively evaluate the risk factors that can play a role before, during or after the surgical period.

NCT ID: NCT04258098 Completed - Colorectal Cancer Clinical Trials

Prophylatic Effect Preoperative Antibiotics With Mechanical Bowel Preparation in SSIs: A Propensity Analysis

Start date: January 1, 2011
Phase:
Study type: Observational

Surgical site infections (SSIs) are a major postoperative complication after colorectal surgery. Current study aims to evaluate prophylactic function of oral antibiotic intake (OA) in combination with mechanical bowel preparation (MBP) relative to MBP alone with respect to postoperative SSIs incidence. A retrospective analysis of eligible patients was to conducted using the databases of the Gastrointestinal Surgery Centre, Third Affiliated Hospital of Sun Yat-sen University from 2011 to 2017. Data pertaining to postoperative hospital stay length, expenses, SSIs incidence, anastomotic fistula incidence, and rates of other complications wloud be extracted and compared. A propensity analysis was conducted to minimize bias associated with demographic characteristics.

NCT ID: NCT04256824 Recruiting - Clinical trials for Surgical Site Infection

Triclosan-antibacterial Sutures Efficacy on the Incidence of Surgical Site Infection in Clean-contaminated Wounds

Start date: February 5, 2020
Phase: Phase 4
Study type: Interventional

Comparing the incidence of SSI in cases using coated Polyglactin 910 suture with Triclosan and cases using Polyglactin 910 suture without Triclosan in clean-contaminated wound surgery