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RECRUITING
NCT03346694
NA

Reducing Surgical Site Infection Rates Using an Alternative Sternal Dressing

Sponsor: Stanford University

View on ClinicalTrials.gov

Summary

This study will evaluate two alternative dressings compared to a standard Island dressing presently in use at Stanford Hospital to determine reductions in surgical site infection (SSI) rates among cardiac surgery patients. Cardiovascular surgery patients who will have a sternotomy incision as a routine part of their surgery will be approached to voluntarily participate. Participants will be randomized to one of three dressing to determine which dressing has the lowest rate of sternal wound infection. The investigators will also assess the impact of alternative dressing use on hospital 30-day readmission rates related to SSI.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

660

Start Date

2018-05-01

Completion Date

2035-05-01

Last Updated

2022-10-26

Healthy Volunteers

No

Conditions

Interventions

DEVICE

Standard Island Dressing

participant randomized to control group before end of surgery to be applied on cardiovascular heart surgical sternal incision.

DEVICE

Prevena Negative Pressure wound dressing

participant randomized to dressing before end of surgery to be applied on cardiovascular heart surgical sternal incision.

DEVICE

Mepilex Border Post-Op Ag

Participant randomized to dressing before end of surgery to be applied on cardiovascular heart surgical sternal incision

Locations (1)

Stanford Healthcare

Stanford, California, United States