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Simulation-based Training for Surgery Residents in Aseptic Techniques (CVC)

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ClinicalTrials.gov Identifier: NCT00787345
Recruitment Status : Completed
First Posted : November 7, 2008
Last Update Posted : September 22, 2010
Sponsor:
Information provided by:
St. Luke's-Roosevelt Hospital Center

Brief Summary:
Central line associated bloodstream infection (CL-ABI) is an important and preventable cause of nosocomial infections and is responsible for considerable morbidity and mortality The Centers for Disease Control have published guidelines for the prevention of CL-ABI that represent a collaborative effort by a multidisciplinary coalition of professional organizations that provide evidence based recommendations to prevent catheter related infections [5]. The interventions emphasize five distinct practices, including: education and training of healthcare providers who place and care for catheters, utilizing maximum sterile barrier precautions during catheter placement.

Condition or disease Intervention/treatment Phase
Nosocomial Infections Other: simulation based training Phase 3

  Show Detailed Description

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 50 participants
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Official Title: General Surgery Residents Education in Maximum Barrier Precautions During Central Venous Catheter Placement: Effect of Simulation-Based Training
Study Start Date : May 2008
Primary Completion Date : July 2010
Study Completion Date : July 2010

Arm Intervention/treatment
Surgery residents
general surgery residents undergoing evaluation and training in MBP during CVC placement as per department policy are eligible for the study.
Other: simulation based training
simulation based training in aseptic techniques that included specified AT categories



Primary Outcome Measures :
  1. Primary outcome: General surgery residents performance in maximal barrier precaution (MBP) technique during central venous catheter (CVC) placement [ Time Frame: 3-6 months ]


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Ages Eligible for Study:   18 Years to 60 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • General surgery residents will be undergoing evaluation and training in MBP according to their department training policy.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00787345


Locations
United States, New York
St.Luke's Roosevelt Hospital
New York, New York, United States, 10019
SLRH
NYC, New York, United States, 10019
Sponsors and Collaborators
St. Luke's-Roosevelt Hospital Center
Investigators
Principal Investigator: Hassan Khouli, MD St. Luke's-Roosevelt Hospital Center

Publications:

Responsible Party: Hassan Khouli, MD, St. Luke's Roosevelt Hospital
ClinicalTrials.gov Identifier: NCT00787345     History of Changes
Other Study ID Numbers: 08-094
First Posted: November 7, 2008    Key Record Dates
Last Update Posted: September 22, 2010
Last Verified: May 2008

Keywords provided by St. Luke's-Roosevelt Hospital Center:
precaution technique during central venous catheter placement.

Additional relevant MeSH terms:
Cross Infection
Infection
Iatrogenic Disease
Disease Attributes
Pathologic Processes