Intraoperative Hygiene Measures and Surgical Site Infections

This study has been completed.
Sponsor:
Information provided by:
University Hospital Inselspital, Berne
ClinicalTrials.gov Identifier:
NCT00555815
First received: November 8, 2007
Last updated: NA
Last verified: November 2007
History: No changes posted

November 8, 2007
November 8, 2007
July 2005
Not Provided
Surgical site infection 30 days postoperative [ Time Frame: 30 days ]
Same as current
No Changes Posted
Adherence to rules of asepsis by members of the surgical team [ Time Frame: intraoperative ]
Same as current
Not Provided
Not Provided
 
Intraoperative Hygiene Measures and Surgical Site Infections
Intraoperative Hygiene Measures and Rates of Surgical Wound Infection in General Surgery

Surgical site infections are associated with high morbidity and cost Hypothesis: Extended intraoperative hygiene measures decrease surgical site infections in general surgery compared to standard hygiene measures.

Intraoperatively two types of hygiene measures were performed randomly: standard and extensive. Standard hygiene measures included empiric accepted measures (e.g. gloves, masks, disinfection). Extensive hygiene measures included among others: double gloving, astro caps, extensive disinfection, extensive intraoperative rinsing. In addition, intraoperative adherence to the rules of asepsis were registered by an independent observer.

Patients were followed for 30 days.

Observational
Observational Model: Cohort
Time Perspective: Prospective
Not Provided
Not Provided
Non-Probability Sample

Consecutive patients undergoing general surgery in university hospital

  • Surgery
  • Surgical Site Infection
  • Hygiene
  • Discipline
  • Colorectal Surgery
Not Provided
  • 1
    Extended hygiene measures
  • 2
    Standard hygiene measures
Beldi G, Bisch-Knaden S, Banz V, Mühlemann K, Candinas D. Impact of intraoperative behavior on surgical site infections. Am J Surg. 2009 Aug;198(2):157-62. Epub 2009 Mar 12.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
1032
January 2007
Not Provided

Inclusion Criteria:

  • Patient undergoing surgical operation in one of two assigned operative theaters. Only initial operations are studied

Exclusion Criteria:

  • Previous inclusion into study
Both
Not Provided
No
Contact information is only displayed when the study is recruiting subjects
Switzerland
 
NCT00555815
1.05.01.30.-17
No
Not Provided
University Hospital Inselspital, Berne
Not Provided
Study Director: Daniel Candinas, MD Department of Visceral and Transplant Surgery
University Hospital Inselspital, Berne
November 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP