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Efficacy Of Copper To Reduce Acquisition Of Microbes and Healthcare-acquired Infections

Medical University of South Carolina (MUSC) logo

Medical University of South Carolina (MUSC)

Status

Completed

Conditions

Healthcare-acquired Infection

Treatments

Other: Copper-alloy surfaced patient care objects

Study type

Interventional

Funder types

Other
Other U.S. Federal agency

Identifiers

NCT01565798
DOD W81XWH-07-C-0053
Effect of Copper on HAI (Other Grant/Funding Number)

Details and patient eligibility

About

CONTEXT: Healthcare-acquired infections (HAI) cause substantial patient morbidity and mortality. Commonly touched items in the patient care environment harbor microorganisms that may contribute to HAI risk. Thus, reduction in the surface bioburden may be an effective strategy to reduce HAI. Inherent biocidal capabilities of copper surfaces offer a theoretical advantage to conventional cleaning, as disinfection is continuous rather than episodic.

OBJECTIVE: Determine whether placement of copper-alloy surfaced objects in an intensive care unit (ICU) reduce risk of HAI.

DESIGN: An intention to treat study where patients are sequentially placed into rooms with or without copper-alloy surfaced objects.

SETTING: The ICUs of three hospitals, a tertiary academic hospital, an academic cancer center, and a Veteran's Administration Medical Center.

PATIENTS: Any patient 18 years of age or older who required admission to an ICU at a study hospital is eligible for placement into a study room if available.

INTERVENTION: Placement of copper-alloy surfaced objects in an ICU room. MAIN OUTCOME MEASURE: Rate of incident HAI and/or colonization with methicillin-resistant Staphylococcus aureus (MRSA) or vancomycin-resistant Enterococcus (VRE) in each type of room.

Enrollment

614 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

patients 18 years and older requiring admission to an ICU at one of the study sites were eligible

Exclusion criteria

  • less than 18 years of age or
  • pregnant

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

Single Blind

614 participants in 2 patient groups

Copper Surfaced Room
Experimental group
Description:
Patients sequentially randomized to this arm were admitted to an ICU room with copper surfaced objects.
Treatment:
Other: Copper-alloy surfaced patient care objects
Standard Surfaced Room
No Intervention group
Description:
Patients sequentially randomized to this arm were admitted to an ICU room with standard surfaced objects

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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