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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01209234
Other study ID # 2010-7710
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2011
Est. completion date January 2019

Study information

Verified date January 2023
Source University of California, Irvine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This randomized controlled trial will compare strategies to reduce the risk of methicillin-resistant Staphylococcus aureus (MRSA) infection and re-hospitalization in MRSA carriers. This trial will provide critical answers about the role of decolonization versus standard-of-care education in preventing MRSA infections in the large group of high risk MRSA-positive patients being discharged from hospitals. Findings could potentially impact best practice for the 1.8 million MRSA carriers who are discharged from US hospitals each year.


Description:

This randomized controlled trial will compare strategies to reduce the risk of methicillin-resistant Staphylococcus aureus (MRSA) infection and re-hospitalization in MRSA carriers. This trial will provide critical answers about the role of decolonization versus standard-of-care education in preventing MRSA infections in the large group of high risk MRSA+ patients being discharged from hospitals. Findings could potentially impact best practice for the 1.8 million MRSA carriers who are discharged from US hospitals each year. Specific Aims: Methicillin-resistant Staphylococcus aureus (MRSA) is arguably the most important single pathogen in healthcare-associated infection when accounting for virulence, prevalence, diversity of disease spectrum, and propensity for widespread transmission. MRSA infection causes or complicates 300,000 hospitalizations each year [Klein, Smith, Laxminarayan], a number which has doubled in the past five years. An additional 1.5 million hospitalized patients either acquire or already harbor the pathogen without current infection. Altogether, these 1.8 million MRSA inpatient carriers experience a high amount of MRSA invasive disease in the year following discharge. Due to increased delivery of complex medical care at home or other post-hospital settings, more and more patients experience serious healthcare-associated morbidity after hospital discharge.[Huang, Platt; Huang, Hinrichsen, Stulgis et al.] In fact, over 80% of patients admitted for MRSA infection have had prior healthcare exposures and are at high risk for repeated MRSA infection.[Huang, Platt; Huang, Hinrichsen, Stulgis et al.; Klevens, Morrison, Nadle, et al.] Project CLEAR compares two strategies to reduce infection and re-hospitalization due to MRSA among patients being discharged from hospitals. Our trial will compare a long-term regimen aimed at eradicating MRSA body reservoirs with patient education on general hygiene and self care, which is the current standard of care. Our specific aims are: - To conduct a randomized controlled trial of serial decolonization versus standard-of-care patient education among MRSA carriers upon hospital discharge to reduce post-discharge MRSA infection and re-hospitalization for one year - To identify predictors of a) infection or re-hospitalization due to MRSA, and b) successful MRSA decolonization, including patient demographics, comorbidities, medical devices, risk behaviors, socioeconomic status, and colonizing MRSA genotype - To estimate medical and non-medical costs of MRSA infection among MRSA carriers and evaluate the potential for cost savings associated with decolonization


Recruitment information / eligibility

Status Completed
Enrollment 2140
Est. completion date January 2019
Est. primary completion date January 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - 1) At least 18 years old - 2) Have had a positive culture (a type of test) for MRSA during recent hospital admission or within the 30 days prior to admission or following discharge - 3) Able to give consent or have a primary caregiver provide consent - 4) Able to bathe or shower or have this consistently performed by a willing caregiver Exclusion Criteria: - 1) Known allergies to chlorhexidine or mupirocin

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Standard-of-Care Education
Patients randomized to standard education will receive a binder with MRSA educational materials which will include or be based upon CDC guidance for MRSA patients at home.
Drug:
MRSA Decolonization
Participants in this arm will be instructed to complete a decolonization regimen that will involve a 5-day application of nasal mupirocin, oral CHG rinse, and CHG body wash twice a month.

Locations

Country Name City State
United States Covington Care Center Aliso Viejo California
United States West Anaheim Extended Care Anaheim California
United States Downey Regional Medical Center Downey California
United States Fountain Valley Regional Hospital & Medical Center Fountain Valley California
United States Orange Coast Memorial Medical Center Fountain Valley California
United States St. Jude Medical Center Fullerton California
United States Chapman Care Center Garden Grove California
United States Pacific Haven HealthCare Center Garden Grove California
United States Regents Point at Windcrest Irvine California
United States Saddleback Memorial Medical Center - Laguna Hills Laguna Hills California
United States Long Beach Memorial Medical Center Long Beach California
United States St. Mary Medical Center Long Beach California
United States Mission Hospital Mission Viejo California
United States Hoag Memorial Hospital Presbyterian Newport Beach California
United States Villa Elena Health Care Center Norwalk California
United States UC Irvine Medical Center Orange California
United States Saddleback Memorial Medical Center - San Clemente San Clemente California
United States Little Company of Mary - San Pedro San Pedro California
United States Country Villa Plaza Santa Ana California
United States Royale Healthcare Santa Ana California
United States Harbor-UCLA Medical Center Torrance California
United States Providence Little Company of Mary Medical Center Torrance California
United States Torrance Memorial Medical Center Torrance California
United States Ventura County Medical Center Ventura California

Sponsors (2)

Lead Sponsor Collaborator
University of California, Irvine Agency for Healthcare Research and Quality (AHRQ)

Country where clinical trial is conducted

United States, 

References & Publications (4)

Huang SS, Hinrichsen VH, Stulgis L, Miroshnik I, Datta R, Watson K, Platt R. Methicillin-resistant Staphylococcus aureus Infection in the Year Following Detection of Carriage (oral presentation). Society of Healthcare Epidemiology of America Annual Meeting (Chicago, IL), March 18-21, 2006.

Huang SS, Platt R. Risk of methicillin-resistant Staphylococcus aureus infection after previous infection or colonization. Clin Infect Dis. 2003 Feb 1;36(3):281-5. doi: 10.1086/345955. Epub 2003 Jan 17. — View Citation

Klein E, Smith DL, Laxminarayan R. Hospitalizations and deaths caused by methicillin-resistant Staphylococcus aureus, United States, 1999-2005. Emerg Infect Dis. 2007 Dec;13(12):1840-6. doi: 10.3201/eid1312.070629. — View Citation

Klevens RM, Morrison MA, Nadle J, Petit S, Gershman K, Ray S, Harrison LH, Lynfield R, Dumyati G, Townes JM, Craig AS, Zell ER, Fosheim GE, McDougal LK, Carey RB, Fridkin SK; Active Bacterial Core surveillance (ABCs) MRSA Investigators. Invasive methicillin-resistant Staphylococcus aureus infections in the United States. JAMA. 2007 Oct 17;298(15):1763-71. doi: 10.1001/jama.298.15.1763. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Number of MRSA Infections Event count of outpatient and inpatient MRSA infections occurring after enrollment 1 year
Other Rehospitalization Due to MRSA Infection Time in days to rehospitalization due to MRSA infection 1 year
Other Cost and Cost Savings Associated With Post-discharge MRSA Decolonization Medical and non-medical costs of MRSA infection within the 1 year follow up period 1 year
Other Number of All-cause Infections (Steering Committee Modified Oct 2011) Event count of all-cause infections occurring after enrollment 1 year
Primary Time to MRSA Infection Time in days to MRSA inpatient or outpatient infection (analyzed with the use of unadjusted Cox proportional-hazard models to identify time to infection; the results we are reporting are number of participants who had an infection event at one year post discharge) 1 year
Secondary Time to All-cause Infection (Steering Committee Modified Oct 2011) Time in days to all-cause infection (analyzed with the use of unadjusted Cox proportional-hazard models to identify time to infection; the results we are reporting are number of participants who had an infection event at one year) 1 year
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