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Skin Cleansing With Chlorhexidine to Decrease Hospital Acquired Infections

This study has been completed.

Sponsors and Collaborators: John H. Stroger Hospital
Sage Products, Inc.
Centers for Disease Control and Prevention
Information provided by: John H. Stroger Hospital
ClinicalTrials.gov Identifier: NCT00130221
  Purpose

Patients in the intensive care unit are at risk for many infections because the severity of illness and the procedures necessary to care for them. This study is designed to look at a change in bathing procedure as a method to reduce infections. Currently, patients at John H. Stroger Hospital are cleansed with soap and water. However, preliminary data from a previous study at Rush University Medical Center showed that a chlorhexidine (CHG)-impregnated cloth (2% CHG Antiseptic Cloth system, Sage Products, Inc.) decreased skin bacteria and may lessen bacteria in the blood stream. The 2% CHG Antiseptic Cloth system is a non-irritating, no-rinse, cleansing and moisturizing product that contains 2% chlorhexidine gluconate. The goal of this proposed study is to further evaluate the effectiveness of the 2% CHG Antiseptic Cloth system compared with soap and water in cleansing the skin and preventing bacteria from entering the bloodstream.


Condition Intervention Phase
Nosocomial Infection
Bacteremia
Sepsis
Pneumonia
Urinary Tract Infection
Clostridium Infection
Drug: 2% chlorhexidine gluconate impregnated cloth
Phase I

MedlinePlus related topics:   Pneumonia    Sepsis    Urinary Tract Infections   

ChemIDplus related topics:   Chlorhexidine    Chlorhexidine digluconate    D-Gluconic acid, monosodium salt    Gluconic acid    Manganese gluconate   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Prevention, Randomized, Open Label, Active Control, Crossover Assignment, Efficacy Study
Official Title:   Skin Cleansing With Chlorhexidine to Improve Nosocomial Infection Risks. (SCCIN Project)

Further study details as provided by John H. Stroger Hospital:

Primary Outcome Measures:
  • Clinical: Primary blood stream infections and culture negative sepsis
  • Microbiologic: Skin colonization from environment and endotracheal secretions

Secondary Outcome Measures:
  • Clinical: Laboratory confirmed blood stream infections
  • Nosocomial infections

Estimated Enrollment:   208
Study Start Date:   June 2005
Study Completion Date:   July 2006

Detailed Description:

Patients admitted to the medical intensive care unit at John H Stroger Hospital are randomly assigned to Unit A or B. Unit B was randomly selected as the intervention unit. For 6 months, all patients in Unit B will be bathed with the 2% CHG Antiseptic Cloth system and all patients in Unit A will receive soap and water baths. After this 6 month period, there will be a 2 to 4 week washout period and the interventions will cross over, with Unit A receiving Chlorhexidine baths and unit B receiving soap and water for 6 months.

Each week, two randomly selected patients will have cultures of the inguinal area, neck/subclavian region, and endotracheal aspirates. A comparison of the colonization of the skin and sputum will be done between the two intervention groups.

Daily infection surveillance will be done on all patients in the intensive care unit. A comparison of blood stream infections, clinical sepsis, and other nosocomial infections will be done between the two intervention groups.

  Eligibility
Ages Eligible for Study:   16 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

  • Data collection will be compiled from all the participants admitted to the Medical Intensive Care Unit (MICU).
  • For skin cultures: One randomly selected (intubated or non-intubated) patient in each intervention group

Exclusion Criteria:

  • Patients with greater than 20% of body surface area disruption in skin integrity will be excluded from participation in the 2% CHG Antiseptic Cloths arm of the study
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00130221

Locations
United States, Illinois
John H. Stroger Hospital of Cook County    
      Chicago, Illinois, United States, 60612

Sponsors and Collaborators
John H. Stroger Hospital
Sage Products, Inc.
Centers for Disease Control and Prevention

Investigators
Principal Investigator:     Robert A Weinstein, MD     John H. Stroger Hospital of Cook County    
  More Information

Publications:

Publications indexed to this study:

Study ID Numbers:   05-006, IND # 71,948
First Received:   August 12, 2005
Last Updated:   April 3, 2007
ClinicalTrials.gov Identifier:   NCT00130221
Health Authority:   United States: Food and Drug Administration

Keywords provided by John H. Stroger Hospital:
Chlorhexidine  
Blood stream infections  
central venous catheter associated  
Nosocomial infection  
Bacteremia  
sepsis  
Pneumonia  
Urinary tract infection
Clostridium Difficile
intensive care unit
catheter
nosocomial pneumonia
Infection control

Study placed in the following topic categories:
Bacterial Infections
Systemic Inflammatory Response Syndrome
Chlorhexidine
Urinary Tract Infections
Bacteremia
Inflammation
Sepsis
Gram-Positive Bacterial Infections
Urologic Diseases
Respiratory Tract Diseases
Respiratory Tract Infections
Chlorhexidine gluconate
Lung Diseases
Clostridium Infections
Pneumonia
Cross Infection

Additional relevant MeSH terms:
Anti-Infective Agents
Anti-Infective Agents, Local
Communicable Diseases
Disinfectants
Pathologic Processes
Therapeutic Uses
Infection
Dermatologic Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on September 05, 2008




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