Clinical Trials Directory

Trials / Completed

CompletedNCT01316588

Recolonization Following Preoperative Disinfection Plastic Adhesive Drapes

Recolonization of the Skin Following Pre-operative Disinfection and Impact of the Use of Plastic Adhesive Drapes

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
140 (actual)
Sponsor
Örebro University, Sweden · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Detailed description

The purpose of this study is to measure the time to recolonization intraoperative after preoperative disinfection with chlorhexidine solution in ethanol and to determine evidence of differential bacterial growth with or without plastic adhesive drape as well as with or without microbial sealant on the leg. A RCT study of 140 patients undergoing coronary artery bypass grafting (CABG) and/or aortic valve replacement (AVR) are included. The investigators test the hypothesis that patients randomized to no plastic adhesive drape intraoperatively will have a reduced recolonisation compared to patients with plastic adhesive drape.

Conditions

Interventions

TypeNameDescription
OTHERPlastic adesive drapePlastic adhesive drape intraoperatively on patients skin around the surgical wound on the chest and bare skin on the leg
OTHERMicrobial SealantMicrobial sealant intraoperatively on patients skin around the surgical wound on the leg and bare skin on the chest

Timeline

Start date
2010-08-01
Primary completion
2011-10-01
Completion
2011-10-01
First posted
2011-03-16
Last updated
2016-04-19

Locations

1 site across 1 country: Sweden

Source: ClinicalTrials.gov record NCT01316588. Inclusion in this directory is not an endorsement.