CompletedNot Applicable

A Comparison of Post-Sternotomy Dressings

United States351 participantsStarted 2010-07

Plain-language summary

The purpose of this study was to determine which of three types of dressings, a dry sterile dressing, a metallic silver dressing or an ionic silver dressing provided better patient outcomes for the post-sternotomy cardiac surgery patient population. In this prospective, randomized controlled trial, the hypothesis was that subjects who received either of the silver impregnated dressings would have better outcomes (better wound healing, less discomfort, and less incidence of infection). Investigators also evaluated dressing factors such as adherence, time for application and ease of use.

Who can participate

Age range21 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Adult (at least 21 years of age) inpatients awaiting cardiac surgery or outpatients seen in the pre-surgical testing area prior to admission for surgery * Having surgery at the study setting * English-speaking * Able to understand and give consent * Had the approval of their cardiothoracic surgeon to participate * Had no known sensitivity to silver * Had no known sensitivity to alginates Exclusion Criteria: * Known sensitivity to silver * Known sensitivity to alginates

What they're measuring

Wound Healing

Timeframe: 5 days postoperatively or day of discharge, whichever came first

Trial details

NCT IDNCT02198066

SponsorCarilion Clinic

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2012-08

View on ClinicalTrials.gov More Impaired Wound Healing trials