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Project CLEAR - Changing Lives by Eradicating Antibiotic Resistance (CLEAR)

Primary Purpose

Methicillin-resistant Staphylococcus Aureus

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Standard-of-Care Education
MRSA Decolonization
Sponsored by
University of California, Irvine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Methicillin-resistant Staphylococcus Aureus focused on measuring Methicillin-resistant Staphylococcus aureus, MRSA

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Covington Care Center
  • West Anaheim Extended Care
  • Downey Regional Medical Center
  • Fountain Valley Regional Hospital & Medical Center
  • Orange Coast Memorial Medical Center
  • St. Jude Medical Center
  • Chapman Care Center
  • Pacific Haven HealthCare Center
  • Regents Point at Windcrest
  • Saddleback Memorial Medical Center - Laguna Hills
  • Long Beach Memorial Medical Center
  • St. Mary Medical Center
  • Mission Hospital
  • Hoag Memorial Hospital Presbyterian
  • Villa Elena Health Care Center
  • UC Irvine Medical Center
  • Saddleback Memorial Medical Center - San Clemente
  • Little Company of Mary - San Pedro
  • Country Villa Plaza
  • Royale Healthcare
  • Harbor-UCLA Medical Center
  • Torrance Memorial Medical Center
  • Providence Little Company of Mary Medical Center
  • Ventura County Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

MRSA Decolonization

Education Arm

Arm Description

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.

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. In addition, educational material on hygiene practices to prevent MRSA infection will be provided.

Outcomes

Primary Outcome Measures

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)

Secondary Outcome Measures

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)

Full Information

First Posted
September 23, 2010
Last Updated
January 5, 2023
Sponsor
University of California, Irvine
Collaborators
Agency for Healthcare Research and Quality (AHRQ)
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1. Study Identification

Unique Protocol Identification Number
NCT01209234
Brief Title
Project CLEAR - Changing Lives by Eradicating Antibiotic Resistance
Acronym
CLEAR
Official Title
Project CLEAR - Changing Lives by Eradicating Antibiotic Resistance
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Completed
Study Start Date
January 2011 (undefined)
Primary Completion Date
January 2019 (Actual)
Study Completion Date
January 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, Irvine
Collaborators
Agency for Healthcare Research and Quality (AHRQ)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief 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.
Detailed 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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Methicillin-resistant Staphylococcus Aureus
Keywords
Methicillin-resistant Staphylococcus aureus, MRSA

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
2140 (Actual)

8. Arms, Groups, and Interventions

Arm Title
MRSA Decolonization
Arm Type
Active Comparator
Arm Description
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.
Arm Title
Education Arm
Arm Type
Active Comparator
Arm Description
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. In addition, educational material on hygiene practices to prevent MRSA infection will be provided.
Intervention Type
Behavioral
Intervention Name(s)
Standard-of-Care Education
Intervention Description
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.
Intervention Type
Drug
Intervention Name(s)
MRSA Decolonization
Intervention Description
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.
Primary Outcome Measure Information:
Title
Time to MRSA Infection
Description
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)
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Time to All-cause Infection (Steering Committee Modified Oct 2011)
Description
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)
Time Frame
1 year
Other Pre-specified Outcome Measures:
Title
Number of MRSA Infections
Description
Event count of outpatient and inpatient MRSA infections occurring after enrollment
Time Frame
1 year
Title
Rehospitalization Due to MRSA Infection
Description
Time in days to rehospitalization due to MRSA infection
Time Frame
1 year
Title
Cost and Cost Savings Associated With Post-discharge MRSA Decolonization
Description
Medical and non-medical costs of MRSA infection within the 1 year follow up period
Time Frame
1 year
Title
Number of All-cause Infections (Steering Committee Modified Oct 2011)
Description
Event count of all-cause infections occurring after enrollment
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Susan S Huang, MD, MPH
Organizational Affiliation
University of California, Irivne - School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Covington Care Center
City
Aliso Viejo
State/Province
California
ZIP/Postal Code
92656
Country
United States
Facility Name
West Anaheim Extended Care
City
Anaheim
State/Province
California
ZIP/Postal Code
92804
Country
United States
Facility Name
Downey Regional Medical Center
City
Downey
State/Province
California
ZIP/Postal Code
90241
Country
United States
Facility Name
Fountain Valley Regional Hospital & Medical Center
City
Fountain Valley
State/Province
California
ZIP/Postal Code
92708
Country
United States
Facility Name
Orange Coast Memorial Medical Center
City
Fountain Valley
State/Province
California
ZIP/Postal Code
92708
Country
United States
Facility Name
St. Jude Medical Center
City
Fullerton
State/Province
California
ZIP/Postal Code
92835
Country
United States
Facility Name
Chapman Care Center
City
Garden Grove
State/Province
California
ZIP/Postal Code
92840
Country
United States
Facility Name
Pacific Haven HealthCare Center
City
Garden Grove
State/Province
California
ZIP/Postal Code
92843
Country
United States
Facility Name
Regents Point at Windcrest
City
Irvine
State/Province
California
ZIP/Postal Code
92612
Country
United States
Facility Name
Saddleback Memorial Medical Center - Laguna Hills
City
Laguna Hills
State/Province
California
ZIP/Postal Code
92653
Country
United States
Facility Name
Long Beach Memorial Medical Center
City
Long Beach
State/Province
California
ZIP/Postal Code
90806
Country
United States
Facility Name
St. Mary Medical Center
City
Long Beach
State/Province
California
ZIP/Postal Code
90813
Country
United States
Facility Name
Mission Hospital
City
Mission Viejo
State/Province
California
ZIP/Postal Code
92691
Country
United States
Facility Name
Hoag Memorial Hospital Presbyterian
City
Newport Beach
State/Province
California
ZIP/Postal Code
92658
Country
United States
Facility Name
Villa Elena Health Care Center
City
Norwalk
State/Province
California
ZIP/Postal Code
90650
Country
United States
Facility Name
UC Irvine Medical Center
City
Orange
State/Province
California
ZIP/Postal Code
92868
Country
United States
Facility Name
Saddleback Memorial Medical Center - San Clemente
City
San Clemente
State/Province
California
ZIP/Postal Code
92673
Country
United States
Facility Name
Little Company of Mary - San Pedro
City
San Pedro
State/Province
California
ZIP/Postal Code
90732
Country
United States
Facility Name
Country Villa Plaza
City
Santa Ana
State/Province
California
ZIP/Postal Code
92707
Country
United States
Facility Name
Royale Healthcare
City
Santa Ana
State/Province
California
ZIP/Postal Code
92707
Country
United States
Facility Name
Harbor-UCLA Medical Center
City
Torrance
State/Province
California
ZIP/Postal Code
90502
Country
United States
Facility Name
Torrance Memorial Medical Center
City
Torrance
State/Province
California
ZIP/Postal Code
90505
Country
United States
Facility Name
Providence Little Company of Mary Medical Center
City
Torrance
State/Province
California
ZIP/Postal Code
90732
Country
United States
Facility Name
Ventura County Medical Center
City
Ventura
State/Province
California
ZIP/Postal Code
93003
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
18258033
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.
Results Reference
background
PubMed Identifier
12539068
Citation
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.
Results Reference
background
Citation
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.
Results Reference
background
PubMed Identifier
17940231
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.
Results Reference
background
PubMed Identifier
30763195
Citation
Huang SS, Singh R, McKinnell JA, Park S, Gombosev A, Eells SJ, Gillen DL, Kim D, Rashid S, Macias-Gil R, Bolaris MA, Tjoa T, Cao C, Hong SS, Lequieu J, Cui E, Chang J, He J, Evans K, Peterson E, Simpson G, Robinson P, Choi C, Bailey CC Jr, Leo JD, Amin A, Goldmann D, Jernigan JA, Platt R, Septimus E, Weinstein RA, Hayden MK, Miller LG; Project CLEAR Trial. Decolonization to Reduce Postdischarge Infection Risk among MRSA Carriers. N Engl J Med. 2019 Feb 14;380(7):638-650. doi: 10.1056/NEJMoa1716771.
Results Reference
derived

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Project CLEAR - Changing Lives by Eradicating Antibiotic Resistance

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